[go: up one dir, main page]

WO1997034473A1 - Craf1 (traf-3) isoforms and uses thereof - Google Patents

Craf1 (traf-3) isoforms and uses thereof Download PDF

Info

Publication number
WO1997034473A1
WO1997034473A1 PCT/US1997/005076 US9705076W WO9734473A1 WO 1997034473 A1 WO1997034473 A1 WO 1997034473A1 US 9705076 W US9705076 W US 9705076W WO 9734473 A1 WO9734473 A1 WO 9734473A1
Authority
WO
WIPO (PCT)
Prior art keywords
cells
disease
crafl
protein
smooth muscle
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US1997/005076
Other languages
French (fr)
Other versions
WO1997034473A9 (en
Inventor
Seth Lederman
Dale M. Frank
Aileen M. Cleary
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Columbia University in the City of New York
Original Assignee
Columbia University in the City of New York
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Columbia University in the City of New York filed Critical Columbia University in the City of New York
Priority to AU25939/97A priority Critical patent/AU2593997A/en
Publication of WO1997034473A1 publication Critical patent/WO1997034473A1/en
Publication of WO1997034473A9 publication Critical patent/WO1997034473A9/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/715—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons
    • C07K14/7151—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons for tumor necrosis factor [TNF], for lymphotoxin [LT]
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/569—Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
    • G01N33/56966—Animal cells
    • G01N33/56972—White blood cells
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • G01N33/6893—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • CD40 (1) is a receptor on B cells that interacts with the helper T cell surface protein CD40L (CD40 ligand, also known as T-BAM, gp39, or TRAP) (2-4) .
  • CD40L is found particularly on lymphoid follicle CD4 + T lymphocytes, where it delivers a contact-dependent signal that stimulates B cell survival, growth, and differentiation (2-4) .
  • Signaling through CD40 rescues B cells from apoptosis induced by Fas (CD95) or by cross-linking of the immunoglobulin M (IgM) complex (5) ; it also induces B cells to differentiate and to undergo Ig isotype switching (3) and to express CD80 (B7 or BB- 1) (6) .
  • CD40L-CD40 interaction The crucial role of CD40L-CD40 interaction is illustrated by humans with defects in CD40L, who manifest a serious immune deficiency syndrome, the X- linked hyper-IgM syndrome (HIGMX-1) characterized by an absence of IgG, IgA, and IgE, elevated IgM, and no lymphoid follicles (7) .
  • HIGMX-1 syndrome the X- linked hyper-IgM syndrome characterized by an absence of IgG, IgA, and IgE, elevated IgM, and no lymphoid follicles (7) .
  • the essential roles of CD40L and CD40 in the phenotype of HIGMX-1 syndrome has been confirmed by targeted disruption of either CD40L (8) or CD40 (9) in mice.
  • CD40 is also expressed by follicular dendritic cells (10) , dendritic cells (11) , activated macrophages (12) , epithelial cells (including thymic epithelium) (13), and a variety of tumor cells.
  • CD40 Stimulation of CD40 causes the tyrosine phosphorylation of multiple substrates including Src family kinases such as p53-p56 lyn , activates multiple serine-threonine- specific protein kinases, and induces the phosphorylation of phospholipase C- ⁇ 2 and of phosphoinositol-3' kinase (14) .
  • CD40 ligation also stimulates protein kinase C-independent activation of the mitgen-activated protein kinases (MAPK) family, including the extracellular signal-regulated protein kinases 1 and 2 (ERK) and the c-Jun NH2-terminal kinases (JNK isofor s) (Li, Y.
  • MAPK mitgen-activated protein kinases
  • mice In mice the CD40 cytoplasmic tail is necessary for signaling (15) . Proteins which interact with the cytoplasmic tail of CD40 have been described (H.M. Hu, et al., J. Biol . Chem. 269: 30069 (1994); and G. Mosialos, et al. , Cell 80:389 (1995)) . These proteins are the same as CRAFl .
  • CD40 signaling is known to be complex and may be mediated or modulated by TRAF-2 (Rothe, M. et al . (1995)
  • TRAF-2 signals may be modulated by TANK (or I-TRAF)
  • the present invention provides an isolated CRAFl peptide encoded by the nucleic acid sequence shown from base 169 to base 2381 of Figures 1A-1P or a variant thereof.
  • One embodiment of the present invention is an isoform of the CRAFl peptide.
  • the present invention also provides for a method of inhibiting activation by CD40 ligand of cells expressing CD40 on the cell surface, comprising providing the cells with the CRAFl peptide or variant thereof, the peptide being present in an amount effective to inhibit activation of the cells.
  • the present invention further provides for a method of treating a condition characterized by an aberrant or unwanted level of CD40-mediated intracellular signaling, in a subject, comprising providing the subject with a therapeutically effective amount of a peptide of this invention capable of inhibiting CD40-mediated intracellular signaling in cells bearing CD40 on the cell surface.
  • FIGS 1A-1P Sequence of TRAF-3 (CRAF-1) and Isoforms thereof. Sequence data of CRAFl is shown including cDNA sequence of isoforms of CRAFl including CRAFl-a (p55; p60 isoform) , CRAFl-b (p70; p77 isoform), smaller CRAFl pre-peptides (p5 isoform and pl5 isoform) , and other deletion isoforms and alternative splice possibilities. The DNA and amino acid sequences of such isoforms are also indicated. The base pair number and the amino acid residue number are indicated.
  • FIG. 2A Schematic diagram of the genomic structure of the zinc finger region of CRAF-1.
  • Fig 2B Schematic diagram of the cDNA structure of the zinc finger regions of CRAF-1, CRAF-1 (del aa 218-242) , and CRAF-1 (del aa 191-242) , as indicated.
  • Predicted amino acid sequences of human CRAFl-a (residues 1-568) .
  • FIG. 4 Predicted CRAFl zinc fingers, corresponding to residues 110 to 264.
  • the zinc fingers are numbered consecutively from 1 to 5, proceeding from the amino terminus to the carboxy terminus .
  • the numbering of the amino acids is based on the sequence shown in Figures 1A-1P, in which the initial "M" residue is +1.
  • FIG. 1 Differential expression of CRAFl isoforms in hyper-IgM patients.
  • Western blot analysis Cell lysates from 1 x 10 7 cells of B cell tumor lines (lanes 1-7 non- transformed, 8-12 EBV-transformed) were immunoprecipitated with a rabbit antiserum directed against TRAF-3 (CRAF-1) molecule. Following the SDS- PAGE, the proteins were transferred to a nitrocellulose sheet and probed with the anti-CRAF-1 antiserum. The specificity of this antiserum is demonstrated by the fact that the low molecular weight CRAF-1, p60 CRAF,
  • CD40 is BJAB transfected with CD40 and overexpressing CD40.
  • RCC/CRAF is Ramos CC transfected with and stably expressing a cDNA construct encoding CRAFl-a (TRAF-3- p70) , and overexpressing CRAFl-a mRNA.
  • BL41 is a B cell tumor cell line.
  • the expression of the p60 CRAF-1 is comparable in all the cell lines examined except the EBV-transformed B cells from patient B, in which only trace amounts of the p60 CRAFl was detected. This result shows that p60 CRAFl is normally expressed in B lymphocytes.
  • p70 CRAF A high molecular weight CRAFl, p70 CRAF (TRAF-3-p70) , was identified in EBV-transformed B cells (lanes 9-12) , but not in non-EBV-transformed cell lines. However the expression level of p70 CRAFl varies. In EBV- transformed B cells established from normal B lymphocytes, p70 CRAF is only expressed at low levels
  • FIGS. 7A-7B The Entire TRAF-3 Gene is Encoded on Two pAC clones. A schematic of two pAC clones is illustrated along with peptide-encoding regions.
  • FIG. 1 Complexity of CD40/p80/LT- ⁇ R Interactions with TRAF-3, TRAF-1 and TRAF-2.
  • FIGS 9A-9C Relationship of CRAFl/TRAF-3 Isoforms to Truncated C26 clone and peptide domains.
  • FIGS. 10A-10D 5' -Untranslated Region of Human TRAF-3 Gene with Transcription Regulatory Functions
  • This invention provides for an isolated CRAFl peptide encoded by the nucleic acid sequence shown from base 169 to base 2381 of Figures 1A-1P or a variant thereof.
  • the CRAFl peptide may be an isoform of the CRAFl peptide.
  • the isoform may comprise a p5 peptide, a pi5 peptide, a p55del9 peptide, a p70del9 peptide, a p55del9,10 peptide, a p70del9,10 peptide, a p55del-8,9 peptide, a p70del-8,9 peptide as shown in Figures 1A-1P.
  • the CRAFl peptide may comprise from zero to four zinc finger domains; wherein when the isoform comprises zinc finger domain 1, 2 and 5, the peptide further comprises one or both of zinc finger domains 3 and 4.
  • the isoform may comprise a CRAFl peptide or variant thereof comprising zero, one, two or four zinc finger domains.
  • the peptide may have deleted zinc finger domains 2, 3 and 4.
  • the peptide may have deleted amino acids 191 to 242 or amino acids 313 to 364 as shown in Figures 1A-1P.
  • the peptide may comprise the sequence GARRGRRVREPGLQPSRDFPAGGSRGGRRLFPAPRHGAARGA(E/K) (R/C) CG PRR(Q/R)TRPAPLSRPSGDGP(Q/R)ELLFPK (Seq I.D. No. ) or a variant thereof capable of inhibiting CD40-mediated cell activation.
  • the isoform may have a molecular weight of about 5 kDa or about 15 kDa.
  • CRAFl is also termed “TRAF-3” .
  • CRAFl nucleic acid encompasses the nucleic acid sequence shown in Figures 1A-1P.
  • CRAFl-a is also termed “TRAF-3-p55” or “p55” or “CRAFl (p55)” or “TRAF-3 (p55)” or “CRAFl (p60) ".
  • CRAFl-b is also termed “TRAF-3-p70” or “p70” or “CRAFl (p70)” or “TRAF-3 (p 70)”.
  • P70-i as used herein encompasses all of the isoforms of p70. and p70-i is represented in Figures 1A-1P as the longest isoform of p70.
  • CRAFl gene encompasses a nucleic acid sequence comprising a genomic sequence of a CRAFl nucleic acid.
  • Two embodiments of a CRAFl gene are the sequences contained in the two pAC clone nucleic acid constructs (pAC clone number 34 and pAC clone number 167) which have been deposited on March 21, 1997 with the American Type Tissue Culture Collection (ATCC) , 12301 Parklawn Drive, Rockville, Maryland 20852, U.S.A. under the provisions of the Budapest Treaty for the International Recognition of the Deposit of Microorganism for the Purposes of Patent Procedure.
  • pAC clone no. 34 was accorded ATCC Accession No.
  • CRAFl gene Another embodiment of a CRAFl gene is the human CRAFl gene. A portion of the human CRAFl gene is shown in Figures 1A- 1P from nucleotide numbers 1-2918. Other embodiments of the present invention provide for the homologous murine CRAFl gene, and the analogous homolog CRAFl gene in other species of animals. Further embodiments of a CRAFl gene are the sequences contained in the following deposits: pE, pGM and pZAC which have been deposited on March 21, 1997 with the American Type Tissue Culture Collection (ATCC) , 12301 Parklawn Drive, Rockville, Maryland 20852, U.S.A.
  • ATCC American Type Tissue Culture Collection
  • CRAFl nucleic acid encompasses the DNA nucleic acid sequence shown in Figures 1A-1P from (169- 2381) which encodes CRAFl (p70) or p70-i as designated in Figures 1A-1P.
  • CRAFl nucleic acid comprising DNA, recombinant DNA, cDNA, mRNA or RNA.
  • Another embodiment of the present invention is the reverse complement of CRAFl nucleic acid.
  • a further embodiment of the present invention is a nucleic acid molecule comprising at least a portion of the CRAFl nucleic acid sequence shown in Figures 1A-1P in an antisense orientation.
  • the nucleic acid may be an isolated nucleic acid or a purified nucleic acid which nucleic acid is separated from cellular particles substantially. Such isolation or purification would be known to one of skill in the art, see Sambrook, et al. Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press, Cold Spring Harbor, New York (1989) .
  • One embodiement of this invention is a nucleic acid comprising of a portion of the human CRAFl nucleic acid sequence shown in Figures 1A-1P.
  • Such embodiments may be isoforms (p70-i) of the CRAFl nucleic acid such as deletion mutants, insertion mutants or substitution mutants, wherein portions of the nucleic acid sequence is deleted, inserted or substituted, respectively. Examples of such isoforms are indicated in Figures 1A- 1P, i.e. p5, pl5, p55-l, etc. Further embodiments of this invention are described in Tables 1 and 2 (see Experimental Details section hereinbelow) .
  • /Another embodiment of the present invention is the deposited cDNA clone IHb, ATCC No. 97489.
  • a further embodiment of the present invention are pAC clones which encompass the entire CRAFl genomic sequence or a portion of the CRAFl genomic sequence.
  • This invention provides for a nucleic acid comprising - li ⁇ the cDNA nucleotide sequence of human CRAFl IHb clone (TRAF-3 (p55) ) which was deposited in GenBank with accession number U21092.
  • This plasmid, pBluescriptSKII+/IIIb was deposited on March 21, 1996 with the American Type Culture Collection (ATCC) , 12301 Parklawn Drive, Rockville, Maryland 20852, U.S.A. under the provisions of the Budapest Treaty for the International Recognition of the Deposit of Microorganism for the Purposes of Patent Procedure. Plasmid pBluescriptSKII+/IIIb was accorded ATCC Accession Number 97489.
  • This invention provides for alleles of the CRAFl nucleic acid.
  • This invention provides for human CRAFl nucleic acid (as shown in Figures 1A-1P) and also provides for the homologous murine CRAFl nucleic acid, as well as the homologous CRAFl nucleic acids in other species of animals.
  • the present invention also provides for upstream and downstream regulatory nucleic acid sequences of CRAFl nucleic acid.
  • One embodiment of this invention is shown in Figures 1A-1P from nucleotides 1-168.
  • Another embodiment of the present invention is shown in Figures 1A-1P from nucleotide 2382-2918.
  • Another embodiment of the invention is shown in Figures 2A-2B which shows the 5' untranslated region of human TRAF-3 gene (CRAFl gene) with has been shown to function as a transcriptional regulator or modulator.
  • This upstream sequence capable of being activated to increase expression of a gene (e.g. transactivated) by EBV infection.
  • This sequence and variants thereof may be useful the modulation and/or expression of heterologous genes as part of recombinant, heterologous nucleic acid constructs. Such constructs may be used in gene therapy as described in more detail hereinbelow.
  • the present invention also provides for nucleic acid probes derived from the nucleic acid sequence as shown in Figures 1A-1P and in Tables 1-4. Such probes may be useful in diagnostic testing of subjects for disease states and for determination of levels of CRAFl peptide expression or lack thereof . Such probes may have other uses such as a monitor use in gene therapy or alternative therapy of subjects suffering from a CRAFl related disorder.
  • the present invention also provides for a CRAFl nucleic acid molecule linked to a vector.
  • the vector may be a self-replicating vector or a replicative incompetent vector.
  • the vector may be a pharmaceutically acceptable vector for methods of gene therapy.
  • An example of replication incompetent vector is LNL6 (Miller, A.D. et al. (1989) BioTechniques 7:980-990) .
  • the present invention provides for CRAFl nucleic acid which is produced by polymerase chain reaction (PCR) .
  • PCR polymerase chain reaction
  • An isolated CRAFl nucleic acid may be isolated by using PCR.
  • Such reactions are well known to one of skill in the art.
  • U.S. Patent Nos. 4,754,065; 4,800,159;; 4,683,195 and 4,683,202 provide PCR techniques and methods and these U.S. Patents are hereby incorporated by reference in their entirties.
  • CRAFl peptide encompasses the amino acid sequence shown in Figures 1A-1P encoded by the nucleotide sequence from base 169 to base 2831 (therein termed p70-i) .
  • CRAFl peptide is also termed TRAF-3 peptide (TRAF-3-p55 or CRAFl(p70)) .
  • This invention encompasses isoforms of the CRAFl peptide, the sequence of several of which are shown in
  • FIGS 1A-1P i.e. p5, pl5, p55-i, p55del-9, etc.
  • Such embodiments and further embodiments of isoforms of the CRAFl peptide are described in Tables 1 and 2.
  • Embodiments of CRAFl peptide include peptides produced from alternatively spliced transcripts derived from a CRAFl nucleic acid, CRAFl peptide isoforms with reduced numbers of zinc finger regions, truncated CRAFl peptide.
  • Another embodiment of the present invention is a prematurely terminated CRAFl peptide, e.g. p5 and pl5 as shown in Figures 1A-1P and on Tables 1 and 2.
  • CRAFl nucleic acid may also be a synthetic nucleic acid or a mimetic of a nucleic acid which may have increased bioavailability, stability, potency or decreased toxicity.
  • Such synthetic nucleic acids may have alterations of the basic A, T, C or G or U bases or sugars which make up the nucleotide polymer to as to alter the effect of the nucleic acid.
  • This invention provides an isolated protein comprising a CRAFl peptide (TRAF-3-p70) domain which comprises
  • PRR(Q/R)TRPAPLSRPSGDGP(Q/R)ELLFPK (Seq I.D. No. ), or a variant thereof capable of inhibiting CD40-mediated cell activation ( Figures 1A-1P) .
  • the amino acids in parentheses are alternatives; one amino acid was found to be coded for in the cloned cDNA and the other amino acid was found to be encoded by the genomic sequence. Thus, it is likely that there are polymorphisms at these sites. This is a 71 amino acid sequence encoded by sequence which is found at the amino-terminal domain of CRAFl nucleic acid as shown in Figures 1A-1P.
  • the protein further comprises CRAFl-a (TRAF-3-p55 or CRAFl (p55) ) or a variant thereof adjacent to the carboxy-terminus of the CRAFl-b (TRAF-3-p70 or CRAFl (p55) ) domain.
  • the molecular weight of the CRAFl peptide is about 70 kDa.
  • an isoform of the CRAFl peptide has a molecular weight of about 5 kDa or about 15 kDa.
  • the CRAFl-b (p70) amino terminal domain comprises at least about 71 amino acids. In another embodiment, it comprises from about 120 to about 150 amino acids. Preferably , it comprises 122 amino acids.
  • This invention provides a CRAFl peptide having a molecular weight of about 70 kDa.
  • the CRAFl peptide comprises an amino acid sequence encoded by exons 1-13.
  • the CRAFl peptide comprises an amino acid sequence that is encoded by the exons as shown in the examples in Tables 1 and 2.
  • Variants encompass the following: Variants can differ from naturally occurring CRAFl peptide (TRAF-3 peptide) in amino acid sequence or in ways that do not involve sequence, or both. Variants in amino acid sequence are produced when one or more amino acids are substituted with a different natural amino acid, an amino acid derivative or non-native amino acid. When a nucleic acid molecule encoding the protein is expressed in a cell, one naturally occurring amino acid will generally be substituted for another.
  • Conservative substitutions typically include the substitution of one amino acid for another with similar characteristics such as substitutions within the following groups: valine, glycine; glycine, alanine; valine, isoleucine; aspartic acid,glutamic acid; asparagine, glutamine; serine, threonine; lysine, arginine; and phenylalanine, tyrosine.
  • the non-polar (hydrophobic) amino acids include alanine, leucine, isoleucine, valine, proline, phenylalanine, tryptophan and methionine .
  • the polar neutral amino acids include glycine, serine, threonine, cysteine, tyrosine, asparagine and glutamine.
  • the positively charged (basic) amino acids include arginine, lysine and histidine.
  • the negatively charged (acidic) amino acids include aspartic acid and glutamic acid.
  • variants within the invention are those with modifications which increase peptide stability. Such variants may contain, for example, one or more non- peptide bonds (which replace the peptide bonds) in the peptide sequence. Also included are: variants that include residues other than naturally occurring L-amino acids, such as D-amino acids or non-naturally occurring or synthetic amino acids such as beta or gamma amino acids and cyclic variants. Incorporation of D- instead of L-amino acids into the polypeptide may increase its resistance to proteases. See, e.g., U.S. Patent No. 5,219,990.
  • the protein of this invention may also be modified by various changes such as insertions, deletions and substitutions, either conservative or nonconservative where such changes might provide for certain advantages in their use.
  • variants with amino acid substitutions which are less conservative may also result in desired derivatives, e.g., by causing changes in charge, conformation and other biological properties.
  • substitutions would include for example, substitution of hydrophilic residue for a hydrophobic residue, substitution of a cysteine or proline for another residue, substitution of a residue having a small side chain for a residue having a bulky side chain or substitution of a residue having a net positive charge for a residue having a net negative charge.
  • the derivatives may be readily assayed according to the methods disclosed herein to determine the presence or absence of the desired characteristics.
  • Variants within the scope of the invention include proteins and peptides with amino acid sequences having at least eighty percent homology with the CRAFl upstream protein sequence, or CRAFl-b. More preferably the sequence homology is at least ninety percent, or at least ninety-five percent.
  • Non- sequence modifications may include, for example, in vivo or in vitro chemical derivatization of portions of the protein of this invention, as well as changes in acetylation, methylation, phosphorylation, carboxylation or glycosylation.
  • the protein is modified by chemical modifications in which activity is preserved.
  • the proteins may be a idated, sulfated, singly or multiply halogenated, alkylated, carboxylated, or phosphorylated.
  • the protein may also be singly or multiply acylated, such as with an acetyl group, with a farnesyl moiety, or with a fatty acid, which may be saturated, monounsaturated or polyunsaturated.
  • the fatty acid may also be singly or multiply fluorinated.
  • the invention also includes methionine analogs of the protein, for example the methionine sulfone and methionine sulfoxide analogs.
  • the invention also includes salts of the proteins, such as ammonium salts, including alkyl or aryl ammonium salts, sulfate, hydrogen sulfate, phosphate, hydrogen phosphate, dihydrogen phosphate, thiosulfate, carbonate, bicarbonate, benzoate, sulfonate, thiosulfonate, mesylate, ethyl sulfonate and benzensulfonate salts.
  • ammonium salts including alkyl or aryl ammonium salts, sulfate, hydrogen sulfate, phosphate, hydrogen phosphate, dihydrogen phosphate, thiosulfate, carbonate, bicarbonate, benzoate, sulfonate, thiosulfonate, mesylate, ethyl sulfonate and benzensulfonate salts.
  • This invention provides a method of inhibiting activation by CD40 ligand of cells bearing CD40 on the cell surface, comprising providing the cells with the protein of this invention, the protein being present in an amount effective to inhibit activation of the cells.
  • the present invention further provides a method of inhibiting activation by CD40 ligand of cells expressing CD40 on the cell surface, comprising providing the cells with the peptide of the invention, the peptide being present in an amount effective to inhibit activation of the cells.
  • the cells are provided with the peptide by introducing into the cells a nucleic acid sequence encoding the peptide under conditions such that the cells express an amount of the peptide effective to inhibit activation of the cells.
  • the nucleic acid sequence is operably linked to a transcriptional control sequence recognized by the cell.
  • the nucleic acid sequence may be a plasmid.
  • the CD40-bearing cells may be selected from the group consisting of B cells, fibroblasts, endothelial cells, epithelial cells, T cells, basophils, macrophages, Reed-Steinberg cells, dendritic cells, renal cells, and smooth muscle cells.
  • the B cells may be resting B cells, primed B cells, myeloma cells, ly ⁇ nphocytic leukemia B cells, or B lymphoma cells.
  • the epithelial cells may be keratinocytes.
  • the fibroblasts may be synovial membrane fibroblasts, dermal fibroblasts, pulmonary fibroblasts, or liver fibroblasts.
  • the renal cells may be selected from the group consisting of glomerular endothelial cells, mesangial cells, distal tubule cells, proximal tubule cells, parietal epithelial cells, visceral epithelial cells, cells of a Henle limb, and interstitial inflammatory cells.
  • the parietal epithelial cells may be crescent parietal epithelial cells.
  • the smooth muscle cells may be smooth muscle cells of the bladder, vascular smooth muscle cells, aortic smooth muscle cells, coronary smooth muscle cells, pulmonary smooth muscle cells, or gastrointestinal smooth muscle cells.
  • the gastrointestinal smooth muscle cells may be esophageal smooth muscle cells, stomachic smooth muscle cells, smooth muscle cells of the small intestine, or smooth muscle cells of the large intestine.
  • the invention provides a method of providing a subject with an amount of a CRAF 1 peptide effective to inhibit activation by CD40 ligand of cells bearing CD40 on the cell surface in the subject, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the CRAFl peptide, under conditions such that the cells express in the subject an activation inhibiting effective amount of the peptide.
  • the introducing of the nucleic acid into cells of the subject may comprise a) treating cells of the subject ex vivo to insert the nucleic acid sequence into the cells; and b) introducing the cells from step a) into the subject.
  • the subject may be a mammal.
  • the mammalian subject may be a human.
  • An embodiment of the present invention is a method of treating a condition characterized by an aberrant or unwanted level of CD40-mediated intracellular signaling, in a subject, comprising providing the subject with a therapeutically effective amount of a CRAFl peptide capable of inhibiting CD40-mediated intracellular signaling in cells bearing CD40 on the cell surface.
  • the peptide may be provided by introducing into CD40- bearing cells of the subject, a nucleic acid sequence encoding the peptide under conditions such that the cells express the peptide according to this method.
  • the condition may be organ rejection in a subject receiving transplant organs, or an immune response in a subject receiving gene therapy.
  • the transplant organ may be a kidney, heart or liver.
  • the condition may be a CD40-dependent immune response.
  • the CD40-dependent immune response may be an autoimmune response in a subject suffering from an autoimmune disease.
  • the autoimmune disease may comprise rheumatoid arthritis, Myasthenia gravis, systemic lupus erythematosus, Graves' disease, idiopathic thrombocytopenia purpura, he olytic anemia, diabetes mellitus, a drug-induced autoimmune disease, psoriasis, or hyper IgE syndrome.
  • the drug-induced autoimmune disease may be drug-induced lupus.
  • the immune response may comprise induction of CD23, CD80 upregulation, rescue from CD95-mediated apoptosis, rescue from apoptosis in a subject undergoing chemotherapy against a tumor, or autoimmune manifestations of an infectious disease.
  • the autoimmune manifestations may be derived from Reiter's syndrome, spondyloarthritis, Lyme disease, HIV infections, syphilis or tuberculosis.
  • the condition may be an allergic response.
  • the allergic response may be hay fever or a penicillin allergy.
  • the condition may be dependent on CD40 ligand-induced activation of fibroblast cells.
  • the condition may be selected from the group consisting of arthritis, scleroderma, and fibrosis.
  • the arthritis may be rheumatoid arthritis, non-rheumatoid inflammatory arthritis, arthritis associated with Lyme disease, or osteoarthritis.
  • the fibrosis may be pulmonary fibrosis, hypersensitivity pulmonary fibrosis, or a pneumoconiosis.
  • the pulmonary fibrosis may be pulmonary fibrosis secondary to adult respiratory distress syndrome, drug-induced pulmonary fibrosis, idiopathic pulmonary fibrosis, or hypersensitivity pneumonitis.
  • the pneumoconiosis may be asbestosis, siliconosis, or Farmer's lung.
  • the fibrosis may be a fibrotic disease of the liver or lung.
  • the fibrotic disease of the lung may be caused by rheumatoid arthritis or scleroderma.
  • the fibrotic disease of the liver may be selected from the group consisting of: Hepatitis-C; Hepatitis-B; cirrhosis; cirrhosis of the liver secondary to a toxic insult; cirrhosis of the liver secondary to drugs; cirrhosis of the liver secondary to a viral infection; and cirrhosis of the liver secondary to an autoimmune disease.
  • the toxic insult may be alcohol consumption.
  • the viral infection may be Hepatitis B, Hepatitis C, or hepatitis non-B non- C.
  • the autoimmune disease may be primary biliary cirrhosis, or Lupoid hepatitis.
  • the condition may be dependent on CD40 ligand-induced activation of endothelial cells.
  • the condition may be selected from the group consisting of atherosclerosis, reperfusion injury, allograft rejection, organ rejection, and chronic inflammatory autoimmune diseases.
  • the atherosclerosis may be accelerated atherosclerosis associated with organ transplantation.
  • the chronic inflammatory autoimmune disease may be vasculitis, rheumatoid arthritis, scleroderma, or multiple sclerosis.
  • the condition may be dependent on CD40 ligand-induced activation of epithelial cells.
  • the epithelial cells are keratinocytes, and the condition is psoriasis.
  • the condition may be an inflammatory kidney disease.
  • the inflammatory kidney disease may not be initiated by autoantibody deposition in kidney.
  • the kidney disease may be selected from the group consisting of :membranous glomerulonephritis;summel change disease/acute tubular necrosis,-pauci-immune glomerulonephritis;focal segmental glomerulosclerosis;interstitial nephritis;antitissue antibody-induced glomerular injury;circulating immune- complex disease;a glomerulopathy associated with a multisystem disease; and drug-induced glomerular disease .
  • the antitissue antibody-induced glomerular injury may be anti-basement membrane antibody disease.
  • the circulating immune-complex disease may be selected from the group consisting of:infective endocarditis; leprosy; syphilis; hepatitis B; malaria; and a disease associated with an endogenous antigen.
  • the endogenous antigen may be DNA, thyroglobulin, an autologous immunoglobulin, erythrocyte stroma, a renal tubule antigen, a tumor-specific antigen, or a tumor- associated antigen.
  • the glomerulopathy may be associated with a multisystem disease is selected from the group consisting of: diabetic nephropathy; systemic lupus erythematosus;Goodpasture's disease; Henoch-Sch ⁇ nlein purpura; polyarteritis; Wegener's granulomatosis; cryoimmunoglobulinemia; multiple myeloma; Waldenstr ⁇ m's macroglobulinemia; and amyloidosis.
  • a multisystem disease is selected from the group consisting of: diabetic nephropathy; systemic lupus erythematosus;Goodpasture's disease; Henoch-Sch ⁇ nlein purpura; polyarteritis; Wegener's granulomatosis; cryoimmunoglobulinemia; multiple myeloma; Waldenstr ⁇ m's macroglobulinemia; and amyloidosis.
  • the pauci-immune glomerulonephritis may be ANCA+ pauci- immune glomerulonephritis, or Wegener's granulomatosis.
  • the interstitial nephritis may be drug-induced interstitial nephritis.
  • the kidney disease may affect renal tubules.
  • the kidney disease which affects renal tubules may be selected from the group consisting of : a kidney disease associated with a toxin; a neoplasia;hypersensitivity nephropathy; Sj ⁇ gren's syndrome; andAIDS.
  • the condition may be a smooth muscle cell-dependent disease.
  • the smooth muscle cell-dependent disease may be a vascular disease.
  • the vascular disease may be atherosclerosis.
  • the smooth muscle cell-dependent disease may be a gastrointestinal disease.
  • the gastrointestinal disease may be selected from the group consisting of esophageal dys otility, inflammatory bowel disease, and scleroderma.
  • the smooth muscle cell- dependent disease may be a bladder disease.
  • the condition may be associated with Epstein-Barr virus.
  • the condition may be selected from the group consisting of mononucleosis, B cell tumors, Burkitt's lymphoma, and nasopharyngeal carcinoma.
  • the treatment may not increase susceptibility of the subject to pneumocystis pneumonia, atypical infections, or tumors.
  • the present invention provides for an isolated nucleic acid molecule encoding a CRAFl peptide.
  • the nucleic acid molecule may be DNA, RNA, cDNA, recombinant DNA, or mRNA.
  • One embodiment of the invention is a vector comprising the CRAFl nucleic acid molecule or variants or isoforms thereof operably linked to a transcriptional control sequence recognized by a host cell transformed with the vector.
  • the vector may be a plasmid.
  • the present invention provides a method of differentiating a subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes, comprising: detecting in an extract from a cell derived from the subject, the presence of a nucleic acid encoding the abnormal CD40 receptor-associated factor, thereby differentiating the subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes.
  • the abnormal CD40 receptor-associated factor polypeptide may be abnormal CD40 receptor-associated factor 1.
  • the subject may be heterozygous for the abnormal CD40 receptor-associated factor.
  • the subject may express CD40 ligand normally.
  • the subject may be a human.
  • the cell may be a B cell.
  • the cell may be derived from a cell culture.
  • the cell may be derived from a bodily fluid.
  • the nucleic acid may encode a truncated CD40 receptor-associated factor polypeptide.
  • the nucleic acid may encode the CD40 receptor-associated factor truncated at the carboxy terminus.
  • the CD40 receptor- associated factor polypeptide may be truncated by at least about 170 amino acid residues.
  • the CD40 receptor- associated factor polypeptide may be truncated by at least about 244 amino acid residues.
  • the nucleic acid may encode the CD40 receptor-associated factor truncated at the amino terminus.
  • the CD40 receptor-associated factor polypeptide may be truncated by at least about 100 amino acid residues.
  • the nucleic acid in the extract may be mRNA, DNA.
  • the method may further comprise amplifying the nucleic acid prior to detecting, and wherein the detecting is detecting of the amplified nucleic acid.
  • the detecting may comprise: contacting the nucleic acid to be detected with a probe, wherein, if the nucleic acid to be detected is DNA, the probe is capable of hybridizing to a coding or noncoding strand of a unique sequence encoding a normal CD40 receptor-associate factor; and if the nucleic acid to be detected is RNA, the probe is capable of hybridizing to a unique sequence encoding a normal CD40 receptor-associated factor, under stringent conditions which would permit hybridization with the unique sequence if present; and detecting the absence of a hybrid of the probe and the nucleic acid to be detected, thereby detecting the nucleic acid encoding the abnormal CD40 receptor-associated factor.
  • the probe may comprise at least nine nucleotides, at least twelve nucleotides, or at least fifteen nucleotides.
  • the probe may be labeled.
  • the label may be a radioactive isotope.
  • the label may be iodine-125.
  • the determining may comprise sequencing the nucleic acid.
  • the present invention provides for a method of providing a subject with an immunosuppressant effective amount of an abnormal CD40 receptor-associated factor, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding an abnormal CD40 receptor-associated factor polypeptide, under conditions such that the cells express in the subject an immunosuppressant effective amount of the abnormal CD40 receptor-associated factor.
  • One embodiment of the present invention is an antibody or portion thereof capable of specifically binding to a CD40 receptor-associated factor.
  • the CD40 receptor- associated factor may be CD40 receptor-associated factor 1.
  • the antibody may be a monoclonal antibody, a chimeric antibody, or a humanized antibody.
  • the portion of the antibody may comprise a complementarity determining region or variable region of a light or heavy chain.
  • the portion of the antibody may comprise a complementarity determining region or a variable region, or a Fab.
  • the present invention provides for a method of differentiating a subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes, comprising: contacting a proteinaceous extract from cells derived from the subject with the antibody or portion thereof under conditions which would permit specific binding of the antibody with normal CD40 receptor-associated factor if present; and detecting the absence of a complex of the antibody with protein in the extract, thereby differentiating a subject with hyper- IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes.
  • the abnormal CD40 receptor-associated factor polypeptide may be abnormal CD40 receptor-associated factor 1.
  • the subject may express CD40 ligand normally.
  • the subject may be a human.
  • the subject may be a murine animal.
  • the cell may be a B cell.
  • the cell may be derived from a cell culture, or from a bodily fluid.
  • the abnormal CD40 receptor-associated factor polypeptide may be truncated.
  • the abnormal CD40 receptor-associated factor may be truncated at the carboxy terminus, or by at least about 170 amino acid residues, or by at least about 244 amino acid residues, or at the amino ⁇ terminus, or by at least about 100 amino acid residues.
  • the antibody or portion thereof may be labeled.
  • the label may be a radioactive isotope such as iodine-125.
  • the present invention also provides a method for killing a tumor cell which comprises contacting the tumor cell with a CRAFl peptide or variant or isoform thereof so as to activate CD40 signaling and thereby kill the tumor cell.
  • the tumor cell may be a breast tumor cell, a prostate cancer tumor cell, a liver cancer cell, a lung cancer cell, a nasoepithelial cancer cell, an EBV induced tumor cell, a nasopharyngeal tumor cell, an esophogeal cancer cell, a colon cancer cell, a gastric cancer cell, a central nervous system tumor cell, an ovarian cancer cell, or a cervical cancer cell.
  • CD40 signaling may be used as a signal for death in transformed cells (Hess, S. and H. Engelmann. 1996. J " . Exp . Med . 183 : 159 ) .
  • This invention provides for a method of performing anti- tumor therapy with CRAFl: CD40 signaling kills tumor cells by apoptosis, particularly when the tumor cell is a non-B cell.
  • This invention provides for a method for treating a subject suffering from a neoplastic condition which comprises administration of a CRAFl peptide or a variant or an isoform thereof in an effective amount so as to kill a tumor cell and thereby treat the neoplastic condition in the subject.
  • the tumor cell may be stimulated to undergo apoptosis.
  • the cell may be in a subject suffering from cancer and the CRAFl peptide or variant or isoform thereof is delivered to the tumor cell.
  • the cells are provided with the protein of this invention by introducing into the cells a nucleic acid sequence encoding the protein under conditions such that the cells express an amount of the protein effective to inhibit activation of the cells.
  • the nucleic acid may be DNA (including cDNA) or RNA. It may be single or double stranded, linear or circular. It may be in the form of a vector such as a plasmid or a viral vector.
  • the nucleic acid sequence is operably linked to a transcriptional control sequence recognized by the host cell.
  • the CD40-bearing cells are selected from the group consisting of B cells, fibroblasts, endothelial cells, epithelial cells, T cells, basophils, macrophages, Reed- Steinberg cells, dendritic cells, myeloma cells, renal cells, and smooth muscle cells.
  • the B cells are resting B cells, primed B cells, myeloma cells, lymphocytic leukemia B cells, or B lymphoma cells.
  • the epithelial cells are keratinocytes.
  • the fibroblasts are synovial membrane fibroblasts, dermal fibroblasts, pulmonary fibroblasts, or liver fibroblasts.
  • the renal cells are selected from the group consisting of glomerular endothelial cells, mesangial cells, distal tubule cells, proximal tubule cells, parietal epithelial cells (e.g., crescent parietal epithelial cells) , visceral epithelial cells, cells of a Henle limb, and interstitial inflammatory cells.
  • the smooth muscle cells are smooth muscle cells of the bladder, vascular smooth muscle cells, aortic smooth muscle cells, coronary smooth muscle cells, pulmonary smooth muscle cells, or gastrointestinal smooth muscle cells.
  • the gastrointestinal smooth muscle cells are esophageal smooth muscle cells, stomachic smooth muscle cells, smooth muscle cells of the small intestine, or smooth muscle cells of the large intestine.
  • This invention provides a method of providing a subject with an amount of the protein of this invention effective to inhibit activation by CD40 ligand of cells bearing CD40 on the cell surface in the subject, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein of this invention, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
  • the introducing of the nucleic acid into cells of the subject comprises: a) treating cells of the subject ex vivo to insert the nucleic acid sequence into the cells; and b) introducing the cells from step a) into the subject.
  • the subject which can be treated by the methods described herein is an animal.
  • the animal is a mammal.
  • Subjects specifically intended for treatment with the method of the invention include humans, as well as nonhuman primates, sheep, horses, cattle, goats, pigs, dogs, cats, rabbits, guinea pigs, hamsters, gerbils, rats and mice, as well as the organs, tumors, and cells derived or originating from these hosts.
  • This invention provides a method of treating a condition characterized by an aberrant or unwanted level of CD40- mediated intracellular signaling, in a subject, comprising providing the subject with an amount of the peptide of this invention capable of inhibiting CD40- mediated intracellular signaling in cells bearing CD40 on the cell surface.
  • the peptide of the present invention may be a protein.
  • the protein is provided by introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
  • the condition is organ rejection in a subject receiving transplant organs.
  • suitable transplant organs include a kidney, heart or liver, as well as others known to those of skill in the art.
  • the condition is an immune response in a subject receiving gene therapy.
  • One difficulty encountered in gene therapy is an immune response by the patient to the gene therapy vector and the proteins it expresses (Yang, Y. et al . (1996) J. Virol. 70:6370) .
  • the protein of this invention inhibits the immune response, gene therapy with the protein of this invention does not trigger an immune response. Its immunosuppressant effect also makes it useful as an adjunct to other forms of gene therapy.
  • the patient is also administered a vector which provides the protein of this invention.
  • condition is an allergic response, including but not limited to hay fever or a penicillin allergy, atopic dermatitis and extrinsic asthma.
  • the immune response comprises induction of CD23, CD80 upregulation, or rescue from CD95-mediated apoptosis.
  • CD40 which is expressed by many tumors, is involved in rescuing cells from apoptosis, inhibitors of CD40- mediated activity are useful as adjunctive agents in chemotherapy.
  • the immune response is autoimmune manifestations of an infectious disease.
  • the autoimmune manifestations are derived from Reiter's syndrome, spondyloarthritis, Lyme disease, HIV infections, syphilis or tuberculosis.
  • the condition is dependent on CD40 ligand-induced activation of fibroblast cells, for example arthritis, scleroderma, and fibrosis.
  • arthritis is rheumatoid arthritis, non-rheumatoid inflammatory arthritis, arthritis associated with Lyme disease, or osteoarthritis.
  • fibrosis is pulmonary fibrosis, hypersensitivity pulmonary fibrosis, or a pneumoconiosis. Examples of pulmonary fibrosis include pulmonary fibrosis secondary to adult respiratory distress syndrome, drug-induced pulmonary fibrosis, idiopathic pulmonary fibrosis, or hypersensitivity pneumonitis.
  • pneumoconiosis examples include asbestosis, siliconosis, or Farmer's lung.
  • the fibrosis is a fibrotic disease of the liver or lung, including fibrotic disease of the lung caused by rheumatoid arthritis or scleroderma, and fibrotic diseases of the liver selected from the group consisting of: Hepatitis-C; Hepatitis-B; cirrhosis; cirrhosis of the liver secondary to a toxic insult; cirrhosis of the liver secondary to drugs; cirrhosis of the liver secondary to a viral infection; and cirrhosis of the liver secondary to an autoimmune disease.
  • the toxic insult is alcohol consumption.
  • the viral infection is Hepatitis B, Hepatitis C, or hepatitis non-B non-C.
  • the autoimmune disease is primary biliary cirrhosis, or Lupoid hepatitis.
  • the condition is dependent on CD40 ligand-induced activation of endothelial cells.
  • the condition dependent on CD40 ligand-induced activation of endothelial cells is selected from the group consisting of atherosclerosis, reperfusion injury, allograft rejection, organ rejection, and chronic inflammatory autoimmune diseases.
  • the atherosclerosis is accelerated atherosclerosis associated with organ transplantation.
  • the chronic inflammatory autoimmune disease is vasculitis, rheumatoid arthritis, scleroderma, or multiple sclerosis.
  • condition is dependent on CD40 ligand-induced activation of epithelial cells.
  • epithelial cells are keratinocytes, and the condition is psoriasis.
  • condition is an inflammatory kidney disease, including inflammatory kidney disease not initiated by autoantibody deposition in kidney and kidney disease which is initiated by autoantibody deposition.
  • the kidney disease is selected from the group consisting of : membranous glomerulonephritis; minimal change disease/acute tubular necrosis; pauci-immune glomerulonephritis; focal segmental glomerulosclerosis; interstitial nephritis; antitissue antibody-induced glomerular injury; circulating immune-complex disease; a glomerulopathy associated with a multisystem disease; and drug-induced glomerular disease.
  • the antitissue antibody-induced glomerular injury is anti-basement membrane antibody disease.
  • the circulating immune-complex disease is selected from the group consisting of: infective endocarditis; leprosy; syphilis; hepatitis B; malaria; and a disease associated with an endogenous antigen.
  • the endogenous antigen is DNA, thyroglobulin, an autologous immunoglobulin, erythrocyte stroma, a renal tubule antigen, a tumor- specific antigen, or a tumor-associated antigen.
  • the glomerulopathy associated with a multisystem disease is selected from the group consisting of: diabetic nephropathy; systemic lupus erythematosus; Goodpasture's disease; Henoch-Sch ⁇ nlein purpura; polyarteritis; Wegener's granulomatosis; cryoimmunoglobulinemia; multiple myeloma; Waldenstr ⁇ m's macroglobulinemia; and amyloidosis .
  • the pauci-immune glomerulonephritis is ANCA+ pauci- immune glomerulonephritis, or Wegener's granulomatosis.
  • the interstitial nephritis is drug- induced interstitial nephritis.
  • the kidney disease affects renal tubules, including but not limited to: a kidney disease associated with a toxin; a neoplasia; hypersensitivity nephropathy; Sjogren's syndrome; and AIDS.
  • the condition is a smooth muscle cell- dependent disease.
  • vascular diseases such as atherosclerosis
  • gastrointestinal diseases such as esophageal dys otility, inflammatory bowel disease, and scleroderma
  • bladder diseases such as atherosclerosis
  • the condition is associated with Epstein-Barr virus.
  • Epstein-Barr virus-associated conditions include mononucleosis, B cell tumors (particularly in immunosuppressed individuals such as chemotherapy patients and those with acquired immune deficiency syndrome (AIDS) ) , Burkitt's lymphoma, and nasopharyngeal carcinoma.
  • Epstein-Barr virus (EBV) transforms cells using latent infection membrane protein 1 (LMP1) .
  • LMP1 binds to CRAFl (also known as LAP1) (33) .
  • Inhibition of the immune response using an antibody against CD40L may potentially making the patient susceptible to pneumocystis pneumonia.
  • Hyper IgM patients who have defective B cell activation signaling do not get pneumocystis pneumonia, other atypical infections, and tumors.
  • the data presented herein indicate that people with the 70 kDa isoform of CRAFl are a subset of these patients. Accordingly, in an embodiment of the above-described method of treating a subject, the treatment does not increase susceptibility of the subject to atypical infections (e.g., pneumocystis pneumonia) or tumors.
  • the nucleic acid may be DNA (including cDNA) or RNA. It may be single or double stranded, linear or circular. It may be in the form of a vector, such as a plasmid or viral vector, which comprises the nucleic acid molecule operably linked to a transcriptional control sequence recognized by a host cell transformed with the vector.
  • the DNA molecule comprises the coding strand of the CRAFl IHb clone ( Figures 1A-1P) .
  • the DNA molecule is complementary to the coding strand of the CRAFl IHb clone.
  • the plasmid is pBluescriptSKII+/IIIb.
  • This invention provides an isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers; wherein when the protein comprises zinc fingers 1, 2 and 5, the protein further comprises one or both of zinc fingers 3 and 4.
  • CRAFl zinc finger domains The numbering of CRAFl zinc finger domains is based on the schematic shown in Figure 4.
  • the zinc finger domains are numbered consecutively from 1 to 5, proceeding from the amino terminus to the carboxy terminus.
  • the zinc fingers if any, in the protein of this invention, may be present in the order in which they appear in wild-type CRAF-1 (e.g., N-l, 3, 4, 5-C) or in a different order (e.g. N-l, 4, 5-C) .
  • a zinc finger domain can be eliminated by deleting the corresponding exon or part of the exon, or by other mutagenesis techniques, for example a point mutation which changes a zinc finger cysteine or histidine to another amino acid which disrupts the zinc finger domain structure.
  • CRAFl proteins or variants thereof comprising from zero to four zinc finger domains of this invention may be capable of inhibiting CD40-mediated cell activation in vitro and in vivo.
  • the protein comprises zero, one, two or four zinc fingers.
  • the protein comprises CRAFl or variant thereof deleted by zinc finger domains 2, 3 and 4, or by exons 8, 9, and 10 in the zinc finger domain encoding region.
  • the protein comprises CRAFl or variant thereof deleted by amino acids 191 to 242.
  • the protein is CRAFla deleted by amino acids 191 to 242 or CRAFlb deleted by amino acids 313 to 364. The deletions of these amino acids result in the formation of new zinc finger domains comprised of different groups of amino acids.
  • the variant comprises a conservative amino acid substitution.
  • Variants can differ from naturally occurring CRAFl and isoforms thereof comprising from one to four zinc fingers, in amino acid sequence or in ways that do not involve sequence, or both.
  • This invention provides a method of inhibiting activation by CD40 ligand of cells bearing CD40 on the cell surface, comprising providing the cells with an isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers, the protein being present in an amount effective to inhibit activation of the cells.
  • the cells are provided with isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers by introducing into the cells a nucleic acid sequence encoding the protein under conditions such that the cells express an amount of the protein effective to inhibit activation of the cells.
  • the nucleic acid may be DNA (including cDNA) or RNA. It may be single or double stranded, linear or circular. It may be in the form of a vector such as a plasmid or a viral vector.
  • the nucleic acid sequence is operably linked to a transcriptional control sequence recognized by the host cell.
  • This invention provides a method of providing a subject with an amount of isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers effective to inhibit activation by CD40 ligand of cells bearing CD40 on the cell surface in the subject, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
  • the protein comprises CRAFl or variant thereof, deleted by amino acids 218 to 242. In specific embodiments the protein is CRAFla deleted by amino acids 218 to 242 or CRAFlb deleted by amino acids 340 to 364. In another embodiment the protein comprises CRAFl or variant thereof, deleted by amino acids 191 to 242. In specific embodiments the protein is CRAFla deleted by amino acids 191 to 242 or CRAF lb deleted by amino acids 313 to 364.
  • the introducing of the nucleic acid into cells of the subject comprises: a) treating cells of the subject ex vivo to insert the nucleic acid sequence into the cells; and b) introducing the cells from step a) into the subject.
  • This invention provides a method of treating a condition characterized by an aberrant or unwanted level of CD40- mediated intracellular signaling, in a subject, comprising providing the subject with an amount of an isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers capable of inhibiting CD40-mediated intracellular signaling in cells bearing CD40 on the cell surface.
  • the protein is provided by introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
  • the condition is a CD40-dependent immune response.
  • the CD40- dependent immune response is an autoimmune response in a subject suffering from an autoimmune disease, including but not limited to rheumatoid arthritis, Myasthenia gravis, systemic lupus erythematosus, Graves' disease, idiopathic thrombocytopenia purpura, hemolytic anemia, diabetes mellitus, a drug-induced autoimmune disease such as drug-induced lupus, psoriasis, hyper IgE syndrome, or abdominal aortic aneurism (AAA) .
  • autoimmune disease including but not limited to rheumatoid arthritis, Myasthenia gravis, systemic lupus erythematosus, Graves' disease, idiopathic thrombocytopenia purpura, hemolytic anemia, diabetes mellitus, a drug-induced autoimmune disease such as drug-induced lupus, psoriasis,
  • the nucleic acid may be DNA (including cDNA) or RNA or mRNA. It may be single or double stranded, linear or circular. It may be in the form of a vector, such as a plasmid or viral vector, which comprises the nucleic acid molecule operably linked to a transcriptional control sequence recognized by a host cell transformed with the vector.
  • the nucleic acid molecule encodes a CRAFl peptide that does not contain exon 9 ( Figures 1A-1P) .
  • the nucleic acid can be a coding strand or complementary to the coding strand or a reverse complement to the coding strand.
  • the CRAFl nucleic acid molecule may be any of the specific sequences shown in Figures 1A-1P and in Tables 1 and 2.
  • This invention provides a method of providing a subject with an amount of a CRAFl protein or variant thereof comprising from zero to four zinc fingers, effective to inhibit activation by CD40 ligand of cells bearing CD40 on the cell surface in the subject, comprising: introducing into CD40-bearing cells of the subject an agent capable of enhancing RNA splicing, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
  • the agent is a splicing apparatus element.
  • the element is a protein; an RNA, for example a a small nuclear RNA (snRNA) ; or a small nuclear ribonucleoprotein (snRNP) .
  • the agent is a vector encoding a splicing apparatus element.
  • the agent can enhance nonspecific RNA splicing, or it can specifically affect CRAFl RNA splicing. In embodiments of this invention the agent enhances downstream splicing, or upstream splicing.
  • the agent enhances formation of a spliceosome, wherein the spliceosome comprises pre-mRNA encoding the CRAFl protein or variant thereof comprising from zero to four zinc fingers.
  • This invention provides a method of differentiating a subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes, comprising: detecting in an extract from a cell derived from the subject, the presence of a nucleic acid encoding the abnormal CD40 receptor-associated factor, thereby differentiating the subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes.
  • abnormal CD40 receptor-associated factor polypeptide is abnormal CD40 receptor-associated factor 1.
  • the expression of mutant or truncated forms of CRAF! Can serve as a dominant negative. Accordingly, in a specific embodiment the subject is heterozygous for the abnormal CD40 receptor-associated factor.
  • the subject with hyper -IgM syndrome expresses CD40 ligand normally.
  • the cell from which the extract is derived is a B cell.
  • the cell may be derived from a cell culture or from a bodily fluid, including but not limited to blood.
  • the gene encoding abnormal CRAF may contain point mutations, frame shift mutations, a premature stop codon. Alternatively, it may be missing a segment of the gene at the 5' or 3' end of the coding region.
  • the nucleic acid encodes a truncated CD40 receptor-associated factor polypeptide.
  • the nucleic acid encodes the CD40 receptor-associated factor truncated at the carboxy terminus.
  • the carboxy-terminal truncated CRAF is truncated by at least about 170 amino acid residues, or by at least about 244 amino acid residues.
  • the nucleic acid encodes the CD40 receptor-associated factor truncated at the amino terminus.
  • the amino-terminal truncated CRAF is truncated by at least about 171 amino acid residues or 258 amino acids.
  • the nucleic acid present in the extract can be RNA or DNA. It can be single stranded or double stranded. In an embodiment the nucleic acid in the extract is mRNA. In another embodiment the nucleic acid in the extract is DNA, including single stranded and double stranded DNA.
  • the nucleic acid is amplified prior to detecting, and the detecting is detecting of the amplified nucleic acid.
  • the nucleic acid is mRNA
  • a cDNA copy is preferably made by reverse transcription.
  • Reverse transcriptase is commercially available, for example from New England Biolabs (Beverly, MA) .
  • PCR a well known laboratory technique (See for example
  • the detecting comprises: contacting the nucleic acid to be detected with a probe, wherein, if the nucleic acid to be detected is DNA, the probe is capable of hybridizing to a coding or noncoding strand of a unique sequence encoding a normal CD40 receptor-associate factor; and if the nucleic acid to be detected is RNA, the probe is capable of hybridizing to a unique sequence encoding a normal CD40 receptor-associated factor, under stringent conditions which would permit hybridization with the unique sequence if present; and detecting the absence of a hybrid of the probe and the nucleic acid to be detected, thereby detecting the nucleic acid encoding the abnormal CD40 receptor-associated factor.
  • the length of the probe should be chosen to provide a high probability that it will recognize a unique sequence. This will depend in part on the length of the genome of the subject and can be easily calculated by one of skill in the art to which this invention pertains.
  • the probe comprises at least nine nucleotides, at least twelve nucleotides, or at least fifteen nucleotides.
  • the probe is labeled.
  • the label is a radioactive isotope. A number of suitable radioactive isotopes are known to those of skill in the art, including but not limited to iodine-125.
  • This invention also provides a method of providing a subject with an immunosuppressant effective amount of an abnormal CD40 receptor-associated factor, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding an abnormal CD40 receptor-associated factor polypeptide, under conditions such that the cells express in the subject an immunosuppressant effective amount of the abnormal CD40 receptor-associated factor.
  • a nucleic acid sequence encoding the protein of interest can be inserted into cells of the subject in vivo.
  • the nucleic acid can be inserted into cells ex vivo and the transfected cells can then be introduced into the subject.
  • the introducing of the nucleic acid into cells of the subject comprises: a) treating cells of the subject ex vivo to insert the nucleic acid sequence into the cells; and b) introducing the cells from step a) into the subject.
  • the abnormal CD40 receptor-associated factor polypeptide is abnormal CD40 receptor-associated factor 1.
  • the nucleic acid sequence encodes a truncated CD40 receptor-associated factor polypeptide.
  • the nucleic acid sequence encodes CD40 receptor-associated factor polypeptide truncated at the amino terminus.
  • the amino-terminal truncated CD40 receptor-associated factor polypeptide is truncated by at least about 171 amino acid residues.
  • the amino-terminal truncated CD40 receptor-associated factor polypeptide is truncated by at least about 323 amino acid residues.
  • nucleic acid sequence encodes CD40 receptor-associated factor polypeptide truncated at the carboxy terminus.
  • carboxy-terminal truncated CD40 receptor-associated factor polypeptide is truncated by at least about 258 amino acid residues.
  • This invention provides a method of inhibiting a CD40- dependent immune response in a subject, comprising providing the subject with an immunosuppressant effective amount of an abnormal CD40 receptor-associated factor by a method which comprises introducing into
  • CD40-bearing cells of the subject a nucleic acid sequence encoding an abnormal CD40 receptor-associated factor polypeptide, under conditions such that the cells express in the subject an immunosuppressant effective amount of the abnormal CD40 receptor-associated factor as described above.
  • the immune response which is inhibited comprises induction of CD23, CD80 upregulation, or rescue from CD95-mediated apoptosis.
  • This invention also provides an antibody or portion thereof capable of specifically binding to a CD40 receptor-associated factor.
  • Techniques for producing antibodies are well known in the art and are described in standard laboratory manuals, such as Harlow and Lane, Antibodies: A Laboratory Manual (Cold Spring Harbor 1988) pp. 53-138.
  • the CRAF protein is preferably coupled to a carrier protein. Examples of useful carrier proteins include keyhole limpet hemacyanin, ovalbumin, bovine serum albumin, mouse serum albumin, and rabbit serum albumin.
  • the CRAF alone or coupled to a carrier protein, is injected into an animal, for example a mouse or rabbit in order to immunize it. Antibodies against the CRAF are then isolated from the immunized animal
  • the CD40 receptor-associated factor is CD40 receptor-associated factor 1.
  • the antibody may be either a polyclonal or monoclonal antibody.
  • the production of monoclonal antibodies using hybridoma technology are well known to those of skill in the art and are described in standard laboratory manuals, such as Harlow and Lane, Antibodies: A Laboratory Manual (Cold Spring Harbor 1988) pp. 139-282.
  • the monoclonal antibody is a chimeric antibody or a humanized antibody.
  • the meaning of "chimeric” and “humanized” antibody and methods of producing them are well known to those of skill in the art and are described, for example, in PCT International Publication No. WO 90/07861, published July 26, 1990 (Queen, et al.) ; and Queen, et al . Proc. Nat'l Acad. Sci. -USA (1989) 86: 10029) .
  • portion of the antibody comprises a complementarity determining region or variable region of a light or heavy chain. In yet another embodiment the portion of the antibody comprises a complementarity determining region or a variable region. In an embodiment the portion of the antibody comprises a Fab.
  • This invention provides a method of differentiating a subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes, comprising: contacting a proteinaceous extract from cells derived from the subject with the antibody or portion thereof as described above under conditions which would permit specific binding of the antibody with normal CD40 receptor-associated factor if present; and detecting the absence of a complex of the antibody with protein in the extract, thereby differentiating a subject with hyper- IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes.
  • abnormal CD40 receptor-associated factor polypeptide is abnormal CD40 receptor-associated factor 1.
  • the subject expresses CD40 ligand normally.
  • the abnormal CD40 receptor-associated factor polypeptide is truncated at the carboxy terminus or the amino-terminus .
  • the carboxy-terminal truncated abnormal CD40 receptor-associated factor polypeptide is truncated by at least about 171 amino acid residues.
  • the abnormal CD40 receptor- associated factor polypeptide is truncated by at least about 244 amino acid residues.
  • the amino-terminal truncated abnormal CD40 receptor-associated factor polypeptide is truncated by at least about 258 amino acid residues.
  • the antibody or portion thereof is labeled.
  • the antibody or portion thereof is labeled with a radioactive isotope.
  • Suitable radioisotopes are known to those of skill in the art and include, but are not limited to iodine-125.
  • Tables 1 and 2 provide some details about several embodiments of the present invention such as exon structure, splice donor and splice acceptor sites, base pair number, etc.
  • Example 1 Complementary DNA Encoding Long CRAFl Isoform
  • cDNA species encoding human CRAFl nucleic acid from a Raj i B cell library (several of which are described in Tables 1 and 2 ) have been isolated that reveal unexpected complexity in the 5' -region of these cDNAs . Although divergent in some cases , comparison of the sequences of these clones suggests at least 8 unique segments, several of which are shared between the cDNA clones and are therefore highly suggestive of alternative splicing events. Given the identity of several distinct cDNA sequence elements between these clones, alternative splicing may account for at least some of these data. However, the formal possibility exists that CRAFl peptide is encoded by several distinct genes.
  • cDNA clone IHb ATCC Accession No. 97489 contains an open reading frame that is not interrupted by a stop codon ( Figures 1A-1P) and Genbank Accession number U21092) .
  • MESSKKD- start site is : ( - 71 - GARRGRRVREPGLQPSRDFPAGGSRGGRRLFPAPRHGAARGA(E/K) (R/C) CG PRR(Q/R)TRPAPLSRPSGDGP(Q/R)ELLFPK-1) (Seq I.D. No. ) .
  • the structure of this domain is highly charged as indicated by the presence of 18/71 arginine residues. It also appears to be an extended strand as evidenced by the presence of 13/71 glycines and 11/71 prolines. In fact, the arginine, glycine and proline content of this putative sub-domain comprises 42/71 of the residues.
  • GenBank does not have homology to any other sequence in GenBank, and does not have an identifiable motif that suggests its function.
  • Two arginine and proline-rich domain motifs have been described (SH.-binding domain, and WW domain) . This sequence does not appear to be either of these two, based on amino acids -71 to -1.
  • the new amino-terminal domain of TRAF-3 p70 described by the first 71 aa has some features of an Src homology 3 (SH3) -binding domain protein (Alexandropoulos, K. , et al. (1995)PNAS, 92:3110; Cohen, G. B., et al. 1995. Cell 80:237) .
  • the sequence aa 103- RPAPLSRP-110 (present in both p70-i and pl5) is similar to the RPLPXXP motif that accounts for SH3- binding in other proteins.
  • the novel amino terminal domain of p70 contains the sequences: 16-PQRP-19 and 44-PCPP-47.
  • RT-PCR was performed on mRNA from three EBV transformed B cell lines; one from a normal subject and two from the HIM patients A and B, by priming the RT reaction with 3'- reverse primer and amplifying with the primer pair oCRf (127-144) /oCRr(675-658) (predicted product (127- 675) for a 548 bp product) .
  • oCRf anneals to a region in exon 2
  • oCRr anneals to the conserved exon 4-13 region shared by all cDNAs.
  • These nucleotide numbers refer to nucleotides in the sequence shown in Figures 1A-1P. Primers in which the first number is higher than the second are reverse nucleotide primers.
  • Two bands were excised from the gel, cloned in the TA system (pCRII, Invitrogen*) and sequenced.
  • the amplified 548 bp band corresponds exactly to sequence of the [exons 2,4-13] product (analogous to IHb) .
  • CD40-L molecules underlie a genetic immune deficiency syndrome, the X-linked hyper-IgM syndrome
  • HIM syndrome does not always involve defects in CD40-L (74,22) .
  • targeted disruption of CD40 results in a phenotype similar to HIM (25,26) .
  • Patients A and B have normal CD40-L expression by the mAb 5c8 and normal expression of CD40 by the mAb G28-5. Both patients A and B are relatively healthy, since they are 49 and 27 years old, respectively, and have not developed neoplastic disease, nor has either had pneumocystis, opportunistic infections or neutropenia, which are features of HIGMX-1 (74) .
  • the peptide products of the CRAFl gene were analyzed using a rabbit antiserum generated to the NH 2 - terminus of the CRAFl peptide.
  • Immunoprecipitation followed by Western blotting with the CRAFl-specific antisera from EBV-transformed B cell lines from a normal individual and from the hyper-IgM patients A, B and C was performed ( Figure 5) .
  • the anti-CRAFl antisera specifically identified peptide species that migrate at 70 kDa and 60 kDa.
  • the expression of the p60 CRAFl is comparable in all the cell lines examined except the EBV-transformed B cells from patient B, in which only trace amounts of the p60 CRAFl was detected. This result shows that p60 CRAFl is normally expressed in B lymphocytes.
  • a high molecular weight CRAFl peptide species, p70 CRAFl (TRAF-3-p70) was identified in EBV- transformed B cells (lanes 9-12) , but not in non-EBV- transformed cell lines. However the expression level of p70 CRAFl varies. In EBV-transformed B cells established from normal B lymphocytes, p70 CRAF is only expressed at low levels (lane 9) .
  • EBV- transformed B cells from patient A the expression of p60 CRAF and p70 CRAFl is comparable (lane 10) .
  • the expression of p70 CRAFl is not only dominant but also dramatically up-regulated.
  • patient B only trace amounts of the p60 CRAFl was detected (lane 11) .
  • the p70 CRAFl expression is below the level of detection (lane 12) .
  • CRAFl Isoforms and cDNA This invention provides various means for determining the amino acid sequence of CRAFl peptide isoforms which are longer than CRAFl-b (CRAFl p70 or TRAF-3-p70) , i.e. which have additional amino acid residues N-terminal to residue -72, as well as nucleic acid sequences coding for such longer isoforms.
  • the IHb clone p55 CRAFl nucleic acid
  • the 70 kDa CRAFl peptide isoform (CRAFl (p70) or TRAF-3-p70) is isolated using an anti- CRAF1 antibody, and its amino terminus sequence determined. Based on the amino-terminal protein sequence, degenerate oligonucleotides are designed which anneal to the corresponding mRNA, cDNA or genomic DNA. Using standard techniques, these degenerate oligonucleotides are used to clone cDNA that encodes the 70 kDa CRAFl peptide isoform.
  • cDNA libraries or genomic libraries are screened for DNA sequences upstream of that shown.
  • the encoded amino acid sequence is deduced based on the DNA sequence of the upstream clone.
  • the upstream sequence can be determined using RACE (Rapid Amplification of cDNA Ends) .
  • RACE kits are commercially available from BOEHRINGER MANNHEIM* and others.
  • First strand cDNA is synthesized from total or poly(A) + RNA using a gene specific primer, reverse transcriptase, and a mixture of deoxynucleotides. After purification from unincorporated nucleotides and primers, terminal transferase is used to add a homolypolymeric A-tail to the 3' end of the cDNA.
  • Tailed cDNA is then amplified by PCR using a gene specific primer and an oligo dT- primer. The cDNA obtained thereby is further amplified. It is then sequenced, and the corresponding protein sequence deduced.
  • the upstream sequence is determined using anchored PCR.
  • anchored PCR is used on the template of Raji cDNA library DNA to identify the sequence further 5'-to what is included in the IHb clone.
  • oCRr 144-126
  • anchoring primers in ⁇ gtll in separate reactions any (since the library is not cloned directionally) of the following are used: o ⁇ gf (1033-1056) (5'-ggT ggC gAC gAC TCC Tgg
  • these PCR amplified cDNA fragments are cloned in the TA cloning system (Invitrogen) and sequenced. The sequences are compared to IHb.
  • the invention features expression vectors for in vivo transfection and expression in particular cell types of CD40 receptor-associated factor truncated at the amino terminus so as to antagonize the function of wild type CD40 receptor-associated factor in an environment in which the wild-type protein is expressed (i.e., introduce abnormal CD40 receptor-associated factor that acts as a dominant negative protein to inhibit CD40 signaling) .
  • Expression constructs of CD40 receptor-associated factor polypeptides may be administered in any biologically effective carrier that is capable of effectively delivering a polynucleotide sequence encoding the CD40 receptor-associated factor to cells in vivo.
  • Approaches include insertion of the subject gene in viral vectors including recombinant retroviruses, baculovirus, adenovirus, adeno-associated virus and herpes simplex virus-1, or recombinant bacterial or eukaryotic plasmids.
  • plasmid DNA can be delivered with the help of, for , example, cationic liposomes or derivatized (e.g., antibody conjugated) polylysine conjugates, gramacidin S, artificial viral envelopes or other such intracellular carriers, as well as direct injection of the gene construct or CaP0 4 precipitation carried out in vivo.
  • cationic liposomes or derivatized (e.g., antibody conjugated) polylysine conjugates e.g., antibody conjugated) polylysine conjugates
  • gramacidin S e.g., artificial viral envelopes or other such intracellular carriers
  • any of the methods known in the art for the insertion of polynucleotide sequences into a vector may be used. See, for example, Sambrook et al. , Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY (1989) and Ausubel et al., Current Protocols in Molecular Biology, J. Wiley & Sons, NY (1992) , both of which are incorporated herein by reference.
  • Conventional vectors consist of appropriate transcriptional/translational control signals operatively linked to the polynucleotide sequence for a particular anti-fibrotic polynucleotide sequence. Promoters/enhancers may also be used to control expression of anti-fibrotic polypeptide.
  • Promoter activation may be tissue specific or inducible by a metabolic product or administered substance.
  • Such promoters/enhancers include, but are not limited to, the native E2F promoter, the cytomegalovirus immediate-early promoter/enhancer (Karasuyama et al. , J. Exp . Med. , 169: 13 (1989) ) ; the human beta-actin promoter (Gunning et al., Proc . Na tl . Acad . Sci . USA, 84: 4831 (1987) ; the glucocorticoid-inducible promoter present in the mouse mammary tumor virus long terminal repeat (MMTV LTR)
  • MMTV LTR mouse mammary tumor virus long terminal repeat
  • Rous sarcoma virus (RSV) (Yamamoto et al . , Cell , 22:787 (1980))
  • HSV herpes simplex virus
  • thymidine kinase promoter (Wagner et al. , Proc . Na tl . Acad . Sci . USA, 78: 1441 (1981))
  • adenovirus promoter (Yamada et al. , Proc . Natl . Acad. Sci . USA, 82: 3567 (1985) ) .
  • Expression vectors compatible with mammalian host cells for use in gene therapy of tumor cells include, for example, plasmids; avian, murine and human retroviral vectors; adenovirus vectors; herpes viral vectors; and non-replicative pox viruses.
  • replication-defective recombinant viruses can be generated in packaging cell lines that produce only replication-defective viruses. See Current Protocols in Molecular Biology: Sections 9.10-9.14 (Ausubel et al. , eds.) , Greene Publishing Associcates, 1989.
  • Preferred vectors are DNA viruses that include adenoviruses (preferably Ad-2 or Ad-5 based vectors) , herpes viruses (preferably herpes simplex virus based vectors) , and parvoviruses (preferably "defective" or non-autonomous parvovirus based vectors, more preferably adeno-associated virus based vectors, most preferably AAV-2 based vectors) .
  • adenoviruses preferably Ad-2 or Ad-5 based vectors
  • herpes viruses preferably herpes simplex virus based vectors
  • parvoviruses preferably "defective" or non-autonomous parvovirus based vectors, more preferably adeno-associated virus based vectors, most preferably AAV-2 based vectors
  • abnormal or wild-type CD40 receptor- assc iated factor may also be introduced into a target cell using a variety of well-known methods that use non- viral based strategies that include electroporation, membrane fusion with liposomes, high velocity bombardment with DNA-coated microprojectiles, incubation with calcium-phosphate-DNA precipitate, DEAE-dextran mediated transfection, and direct micro-injection into single cells.
  • an anti-fibrotic polynucleotide encoding an immunosuppressant effective amount of an abnormal CD40 receptor-associated factor may be introduced into a cell by calcium phosphate coprecipitation (Pillicer et al., Science, 209: 1414- 1422 (1980) ; mechanical microinjection and/or particle acceleration (Anderson et al., Proc. Natl . Acad. Sci . USA, 77: 5399-5403 (1980) ; liposome based DNA transfer
  • CD40 receptor-associated factor itself may also be chemically modified to facilitate its delivery to a target cell.
  • One such modification involves increasing the lipophilicity of the CD40 receptor-associated factor in order to increase cell surface binding and stimulate non-specific endocytosis of the polypeptide.
  • a wide variety of lipopeptides, fatty acids, and basic polymers e.g., tripalmitoyl-S-glycerylcysteil-seryl- serine; palmitic acid; polyarginine
  • lipopeptides, fatty acids, and basic polymers e.g., tripalmitoyl-S-glycerylcysteil-seryl- serine; palmitic acid; polyarginine
  • Delivery may also be effected by using carrier moieties known to cross cell membranes.
  • an abnormal CD40 receptor-associated factor may be fused to a carrier moiety, preferably by genetic fusion, and the fused construct may be expressed in bacteria or yeast using standard techniques.
  • polynucleotide sequences encoding abnormal or wild type CD40 receptor- associated factor useful in the present invention, operatively linked to regulatory sequences may be constructed and introduced into appropriate expression systems using conventional recombinant DNA techniques. The resulting fusion protein may then be purified and tested for its capacity to enter intact target cells and inhibit growth of the target cells once inside the target.
  • recombinant methods may be used to attach a carrier moiety to anti-fibrotic polynucleotide sequences by joining the polynucleotide sequence encoding for abnormal CD40 receptor-associated factor with the polynucleotide sequence encoding a carrier moiety and introducing the resulting construct into a cell capable of expressing the conjugate.
  • Two separate sequences may be synthesized, either by recombinant means or chemically, and subsequently joined using known methods.
  • the entire conjugate may be chemically synthesized as a single amino acid sequence.
  • Useful carrier moieties include, for example, bacterial hemolysins or "blending agents" such as alamethicin or sulfhydryl activated lysins.
  • Other carrier moieties include cell entry components of bacterial toxins such as Pseudomonas exotoxin, tetanus toxin, ricin toxin and diphtheria toxin.
  • Other useful carrier moieties include proteins which are viral receptors, cell receptors or cell ligands for specific receptors that are internalized and cross mammalian cell membranes via specific interaction with cell surface receptors. Such cell ligands include epidermal growth factor, fibroblast growth factor, transferrin and platelet derived growth factor.
  • the carrier moiety may also include bacterial immunogens, parasitic immunogens, viral immunogens, immunoglobulins, and cytokines.
  • purified human immunodeficiency virus type-1 (HIV) tat protein is the carrier moiety.
  • Purified human immunodeficiency virus type-1 (HIV) tat protein is taken up from the surrounding medium by human cells growing in culture. See Frankel et al. , Cell 55: 1189-1193, (1988) ; Fawell et al. , Proc. Natl . Acad. Sci .
  • tat genetic fusion construct (use of tat genetic fusion construct) , all of which are incorporated herein by reference. See also PCT Application Serial Number PCT/US93/07833, published 3 March 1994 which describes the tat-mediated uptake of the papillomavirus E2 repressor; utilizing a fusion gene in which the HIV-1 tat gene is linked to the carboxy- terminal region of the E2 repressor open reading frame.
  • the tat protein can deliver, for example, abnormal or wild type CD40 receptor-associated factor and polynucleotide sequences into cells, either in vitro or in vivo.
  • delivery can be carried out in vitro by adding a genetic fusion encoding an abnormal CD40 receptor-associated factor- tat conjugate to cultured cells to produce cells that synthesize the tat conjugate or by combining a sample (e.g., blood, bone marrow, tumor cell) from an individual directly with the conjugate, under appropriate conditions.
  • the target cells may be vitro cells such as cultured animal cells, human cells or microorganisms. Delivery may be carried out in vivo by administering the CD40 receptor- associated factor and tat protein to an individual in which it is to be used.
  • the target may be in vivo cells, i.e., cells composing the organs or tissue of living animals or humans, or microorganisms found in living animals or humans.
  • the ADP ribosylation domain from Pseudo onas exotoxin ("PE") and pancreatic ribonuclease have been conjugated to tat to confirm cytoplasmic delivery of a protein.
  • the ADP phosphorylation domain is incapable of entering cells so that cytoplasmic delivery of this molecule would be confirmed if cell death occurs.
  • ribonuclease itself is incapable of entering cells so that inhibition of protein synthesis would be a hallmark of intracellular delivery using a tat conjugate.
  • Chemical (i.e., non-recombinant) attachment of CD40 receptor-associated factor polypeptide sequences to a carrier moiety may be effected by any means which produces a link between the two components which can withstand the conditions used and which does not alter the function of either component.
  • Many chemical cross- linking agents are known and may be used to join an abnormal or wild-type CD40 receptor-associated factor polynucleotide sequence or polypeptide to carrier moieties.
  • intermolecular cross-linking agents are, for example, succinimidyl 3- (2- pyridyldithio)propionate (SPDP) or N, N'-(l,2- phenylene)bismaleimide are highly specific for sulfhydryl groups and form irreversible linkages; N, N'- ethylene-bis- (iodoacetamide) (specific for sulfhydryl) ; and 1, 5-difluoro-2 , 4-dinitrobenzene (forming irreversible linkages with tyrosine and amino groups) .
  • SPDP succinimidyl 3- (2- pyridyldithio)propionate
  • N, N'-(l,2- phenylene)bismaleimide are highly specific for sulfhydryl groups and form irreversible linkages
  • N, N'- ethylene-bis- (iodoacetamide) specifically for sulfhydryl)
  • agents include p , p'-difluoro- , m'- dinitrodiphenylsulfone (forming irreversible linkages with amino and phenolic groups) ; dimethyl adipimidate (specific for amino groups) ; hexamethylenediisocyante (specific for amino groups) ; disdiazobenzidine (specific for tyrosine and histidine) ; succinimidyl 4- (N- maleimidomethyl) cyclohexane-1-carboxylate (SMCC) ; m- maleimidobenzoyl-N-hydroxysuccinimide ester (MBS) ; and succinimide 4- (p-maleimidophenyl)butyrate (SMPB) .
  • SMCC N- maleimidomethyl
  • MBS m- maleimidobenzoyl-N-hydroxysuccinimide ester
  • succinimide 4- p-maleimidophenyl)butyrate
  • T h e succinimidyl group of these cross-linkers reacts with a primary amine, and the thiol-reactive maleimide reacts with the thiol of a cysteine residue.
  • the delivery systems for the abnormal or wild-type CD40 receptor-associated factor polynucleotide sequence can be introduced into a patient by any number of methods, each of which is familiar to persons of ordinary skill. Specific incorporation of the delivery system in the target cells occurs primarily from specificity of transfection provided by the gene delivery vehicle, cell type or tissue type expression due to the transcriptional regulatory sequences controlling expression of the polynucleotide, or a combination thereof. In other embodiments, initial delivery of the recombinant gene is more limited with introduction into the animal being localized by, for example, catheter (U.S. Patent 5,328,470) or stereotactic injection (Chen et al . , Proc . Na tl . Acad. Sci . USA, 91: 3054-3057 (1994) .
  • Liposome-mediated DNA transfer See, e.g., Caplen et al., "Liposome-mediated CFTR Gene Transfer To The
  • Retrovirus-mediated DNA transfer See, e.g., Kav et al., "In Vivo Gene Therapy Of Hemophilia B: Sustained Partial Correction In Factor IX-Deficient Dogs", Science. 262, pp. 117-19 (1993) ; Anderson, “Human Gene Therapy", Science, 256, pp. 808-13 (1992) ;
  • DNA viruses include adenoviruses (preferably Ad-2 or Ad-0 based vectors) , herpes viruses (preferably herpes simplex virus based vectors) , baculoviruses, and parvoviruses (preferably "defective" or non- autonomous parvovirus based vectors, more preferably adeno-associated virus based vectors, most preferably AAV-2 based vectors) .
  • adenoviruses preferably Ad-2 or Ad-0 based vectors
  • herpes viruses preferably herpes simplex virus based vectors
  • baculoviruses baculoviruses
  • parvoviruses preferably "defective" or non- autonomous parvovirus based vectors, more preferably adeno-associated virus based vectors, most preferably AAV-2 based vectors
  • Adenoviruses can infect quiescent or terminally differentiated cells, such as neurons or hepatocytes, and appear essentially non-oncogenic. See, e.g., Ali et al., Supra. p. 367. Adenoviruses do not appear to integrate into the host genome. Because they exist extrachromosomally, the risk of insertional utagenesis is greatly reduced. Ali et al., Supra, p. 373. Adeno- associated viruses exhibit similar advantages as adenoviral-based vectors. However, AAVs exhibit site- specific integration on human chromosome 19. Ali et al., supra. p. 377.
  • the pharmaceutical preparation of the gene therapy construct can consist essentially of the gene delivery system in an acceptable diluent, or can comprise a slow release matrix in which the gene delivery vehicle is embedded. Where the complete gene delivery system can be produced intact from recombinant cells such as retroviral vectors, the pharmaceutical preparation can include one or more cells which produce the gene delivery system.
  • Effective amounts of the compounds of the invention may be administered in any manner which is medically acceptable.
  • the method of administration may include injections, by parenteral routes such as intravenous, intravascular, intraarterial , subcutaneous, intramuscular, intratumor, intraperitoneal , intraventricular, intraepidural, or others as well as oral, nasal, ophthalmic, rectal, topical, or inhaled.
  • pharmaceutically acceptable carrier means one or more organic or inorganic ingredients, natural or synthetic, with which the molecule is combined to facilitate its application.
  • a suitable carrier includes sterile saline although other aqueous and non-aqueous isotonic sterile solutions and sterile suspensions known to be pharmaceutically acceptable are known to those of ordinary skill in the art.
  • the term “pharmaceutically acceptable carrier” means one or more organic or inorganic ingredients, natural or synthetic, with which the molecule is combined to facilitate its application.
  • a suitable carrier includes sterile saline although other aqueous and non-aqueous
  • carrier encompasses liposomes or the HIV-1 tat protein
  • an effective amount refers to that amount which is capable of ameliorating or delaying progression of the diseased, degenerative or damaged condition.
  • An effective amount can be determined on an individual basis and will be based, in part, on consideration of the symptoms to be treated and results sought. An effective amount can be determined by one of ordinary skill in the art employing such factors and using no more than routine experimentation.
  • an effective amount of the abnormal or wild-type CD40 receptor-associated factor in preferred methods, an effective amount of the abnormal or wild-type CD40 receptor-associated factor
  • CRAFl peptide (contained within its attendant vector; i.e., "carrier) may be directly administered to a target cell or tissue via direct injection with a needle or via a catheter of other delivery tube placed into the cell or tissue. Dosages will depend primarily on factors such as the condition being treated, the selected polynucleotide, the age, weight, and health of the subject, and may thus vary among subjects.
  • An effective amount for a human subject is believed to be in the range of about ⁇ .l ml to about 50 ml of saline solution containing from about 1 x 10 7 to about 1 x 10 11 plaque forming units (pfu) /ml CD40 receptor-associated factor polynucleotide (CRAFl nucleic acid) containing, viral expression vectors.
  • pfu plaque forming units
  • Target cells treated by abnormal or wild-type CD40 receptor-associated factor polynucleotide sequences may be administered topically, intraocularly, parenterally, intranasally, intratracheal, intrabronchially, intramuscularly, subcutaneously or by any other means.
  • Target cells to be treated by abnormal or wild-type CD40 receptor-associated factor protein may be administered topically, intraocularly, parenterally, intranasally, intratracheal, intrabronchially, intramuscularly, subcutaneously or by any other means.
  • the protein compounds of the invention are administered at any dose per body weight and any dosage frequency which is medically acceptable.
  • Acceptable dosage includes a range of between about 0.01 mg/kg and about 500 mg/kg subject body weight.
  • a preferred dosage range is between about 1 and about 100 mg/kg.
  • Particularly preferred is a dose of between about 1 and about 30 mg/kg.
  • the dosage is repeated at intervals ranging from each day to every other month.
  • One preferred dosing regime is to administer a compound of the invention daily for the first three days of treatment, after which the compound is administered every 3 weeks, with each administration being intravenously at about 5 or about 10 mg/kg body weight.
  • Another preferred regime is to administer a compound of the invention daily intravenously at about 5 mg/kg body weight for the first three days of treatment, after which the compound is administered subcutaneously or intramuscularly every week at about 10 mg per subject.
  • the protein compounds of the invention similarly to the therapeutic nucleotide sequences, may be delivered to tissues in a liposome-encapsulated formulation, or conjugated to carrier moieties such as HIV tat protein. This delivery can be systemic, such as by intravascular delivery, or local. Local means of delivery of liposome-encapsulated compounds of the invention include intratumor or intraorgan injection.
  • catheter such as intrahepatic delivery into the portal vein, intrarenal or intraprostate delivery via the urethra, intracholecystic delivery via the bile duct, or delivery into various blood vessels of interest, particularly the coronary vessels or sites of vascular stenosis.
  • Targeted delivery may be accomplished by inserting components into the surface of the liposomes or other carrier moieties which confer target specificity. For example, areas of inflammation might be targeted by coating the carrier liposomes with monoclonal antibodies specific for anti-CD40 ligand.
  • Various types of tumors could be selectively targeted by coating liposomes with monoclonal antibodies specific for surface antigens characteristic of the tumor cells.
  • the liposome system may be any variety of unilamellar vesicles, multilamellar vesicles, or stable plurilamellar vesicles, and may be prepared and administered according to methods well known to those of skill in the art, for example in accordance with the teachings of United States Patents 5,169,637, 4,762,915, 5,000,958 or 5,185,154, which are hereby incorporated by reference.
  • the proteins of this invention may be used in the form of a pharmaceutically acceptable salt
  • suitable acids and bases which are capable of forming salts with the polypeptides of the present invention are well known to those of skill in the art, and include inorganic and organic acids and bases.
  • the compounds of the invention may be administered as a single dosage for certain indications such as preventing immune response to an antigen to which a subject is exposed for a brief time, such as an exogenous antigen administered on a single day of treatment.
  • an antigen would include coadministration of a compound of the invention along with a gene therapy vector, or a therapeutic agent such as an antigenic pharmaceutical or a blood product.
  • the compounds of the invention are administered at intervals for as long a time as medically indicated, ranging from days or weeks to the life of the subject.
  • Example 2 Alteration of Expression of CRAFl-encoded Gene Products Are Associated with Hyper-IgM Syndrome (Low or Absent IgG, IgA. IgE) : Target Validation for CRAFl as a target for Immunosuppressive Therapy
  • Patient A,B and C Three individuals with non-X linked HIM (Patients A,B and C) that have normal CD40-L expression by the mAb 5c8 (and in the case of patient B by sequence analysis and normal expression of CD40 by the mAb G28-5 were analyzed. Both patients A and B are relatively healthy, since they are 49 and 27 years old, respectively, and have not developed neoplastic disease, nor has either had pneumocystis, opportunistic infections or neutropenia, which are features of HIGMX-1 (37) . Patient C is younger but is relatively healthy.
  • CRAFl Since NH--terminal truncations in CRAFl act as dominant negatives in cell culture (26) , studies were undertaken to determine whether CRAFl mutations are associated with HIM in individuals with normal expression of CD40-L. Therefore, EBV-transformed lymphoblastoid cell lines were generated from the patients and patient C's mother. The B cell lines from these 3 unrelated patients with HIM (and the mother of patient C) were used to determine the sequence of CRAFl mRNA by RT-PCR. Sets of oligonucleotides designed to sequence CRAFl were selected that amplified four overlapping regions of the CRAFl cDNA.
  • CRAFl peptides Analysis of CRAFl peptides in HIM patients Analysis of CRAFl encoded peptides has recently become possible because of the availability of anti-CRAFl antisera. Therefore, this antisera was used to determine if protein products of the potentially mutated alleles are present in cells from these individuals.
  • a rabbit antiserum generated to the NH 2 -terminus of the CRAFl peptide was used to perform immunoprecipitation of metabolically labeled Ramos cells, Ramos/pCEP/CRAFl and EBV-transformed B cell lines [pCEP is an expression vector available from Invitrogen] .
  • the lysates from the patient A cell line also contains the 60 kDa band, suggesting that if this patient has a mutated allele, a normal allele may also be present. It is unknown if the predicted 70 kDa peptide is relatively unstable or if some other process (potentially compensatory) is occurring in these cells, that would result in the 77 kDa (p70 or p77) band by a complex process, such as alternative splicing to delete a exon 3 that contains an in-frame termination codon. The Western blot data in Figure 5 suggests that p70 may not be rapidly degraded, since patient A has p70 peptide with a low rate of p70 synthesis.
  • CD23 and CD80 on Ramos/pCEP/CRAFl transfectants shows that CD23 expression is not upregulated (relative to Ramos/pEBVHIs/lacZ controls ( Figure 3) .
  • Figure 3 The cell surface expression of CD23 and CD80 on Ramos/pCEP/CRAFl transfectants shows that CD23 expression is not upregulated (relative to Ramos/pEBVHIs/lacZ controls ( Figure 3) .
  • These data indicate that expression of full length CRAFl does not induce the phenotype of a constitutively CD40-activated B cell, at least with respect to CD23 and CD80.
  • CD40-triggering was induced by coculture with 293/CD40-L cells (or control 293/CD8 cells, not shown) .
  • Ramos/pCRAFl cells In response to CD40 triggering with 293/CD40-L cells, Ramos/pCRAFl cells have normal responsiveness with respect to upregulation of CD23 or CD80 or ICAM1.
  • the Ramos cells over-expressing the clones were triggered with 293/CD40-L * cells and the expression of CD23 and CD80 was measured by two-color FACS.
  • the transfected clones were deficient at upregulating CD23 in response to stimulation with 293/CD40-L * cells relative to control Ramos cells or Ramos cells expressing full length CRAFl.
  • CD40-mediated upregulation of CD80 (which has been shown to correlate with the induction of co-stimulatory activity by B-CLL cells (see above) ) appears to depend in large part on CRAFl signaling.
  • CD40 triggering also induces upregulation of CD54 (ICAM1) (40) and homotypic aggregation, but these effects are not inhibited by overexpression of the CRAFl dominant negative C26-1 fusion protein.
  • ICAM1 CD54
  • CRAFl signaling The complete predicted aa sequences of human and mouse CRAFl are highly homologous and reveal a Zn** ring domain, a Zn ** finger domain, a coiled-coiled domain and importantly, that the -CO ⁇ -terminal domain that binds the CD40 cytoplasmic tail is homologous to two recently identified proteins, "TNF ⁇ Receptor-Associated Factors" 1 and 2 (TRAF-1 and TRAF-2) that form a complex with the cytoplasmic tail of TNFR ⁇ ll (41) .
  • TRAF-1 and TRAF-2 TRAF-1 and TRAF-2
  • the phenotype of the transfectants is analyzed (to determine whether constitutive activation of CD23 and/or CD80 expression is present) or CD40- triggered functional assays are performed to analyze the potential dominant negative effects of these constructs. Analysis of constitutive activation may be carried out by evaluating and detecting relative amounts of tumor cell death.
  • One possible outcome of these experiments is that overexp ession of the Zn ring and finger domains in isolation from other domains, will result in constitutive activation of Ramos cells (i.e., constitutive high expression of CD23 and CD80) . This would be taken to suggest that CD40-signaling may activate CRAFl by proteolysis which would liberate the DNA binding domain.
  • CD40 is a cell surface receptor for the T helper effector molecule, CD40-L (T-BAM, gp39, TRAP) and this interaction is essential for B cell selection and differentiation in vitro and in vivo.
  • a protein that binds to the cytoplasmic tail of CD40 termed "CD40 Receptor Associated Factor 1"(CRAFl) has been identified. Stable overexpression of the 240aa carboxy terminus of CRAFl as a fusion protein (C26) in Ramos 2G6 B cells inhibits the CD40-dependent induction of CD23 expression
  • Ramos B cells expressing the C26 fusion protein or control (expressing lacZ) were stimulated with anti-CD40 mAb (G28-5) and assessed for their ability to be rescued from Fas (CD95) -mediated apoptosis
  • C26 inhibits anti-CD40 mediated rescue from Fas-mediated apoptosis and inhibits anti-CD40 mediated CD80 upregulation.
  • C26 does not affect CD40-mediated CD54 upregulation nor homotypic aggregation, suggesting that the CD54 upregulation pathway is either less sensitive to C26 inhibition or possibly that CD40 has alternative (non-CRAFl) mediated signaling.
  • non-CRAFl non-CRAFl mediates the CD40 signals for rescue from apoptosis and upregulation of CD80, however, the CD40 signals for inducing ICAM are unresolved.
  • CD40-L is known to have a different role from CD95 in germinal center biology because mutations in CD40-L impair germinal center formation as manifest in humans that have absent or mutant CD40-L protein expression (X- linked, hyper-IgM syndrome (HIGMX-1) or mice with targeted disruptions of CD40-L or CD40.
  • HIGMX-1 X- linked, hyper-IgM syndrome
  • mice with targeted disruptions of CD40-L or CD40 X- linked, hyper-IgM syndrome
  • the lack of germinal centers in HIGMX-1 is associated with extensive IgM+ B cell infiltration of tissues, particularly in the GI tract (11,13-18,20), which may relate to the predisposition of HIGMX-1 patients to develop polyclonal B cell pseudolymphomas (11,13) .
  • the mAb 5c8 (anti-CD40-L) has been described (1) .
  • the following mAb were produced from hybridomas available from the American Type Culture Collection (Rockville, MD) : 0KT8 (anti-CD8), DA4-4 (anti-IgM) and W6/32 (anti- MHC class I) . These mAb were purified from ascites fluid on protein A (Biorad, Rockville Center, NY) or protein G columns (Pharmacia, Upsula, Sweden) .
  • Leu-16 (Anti-CD20) mAb conjugated to flourescein and Leu-17 (Anti-CD38) mAb conjugated to PE were purchased from Becton Dickinson (Mountainview, CA) .
  • BB20 (anti-CD40) was purchased from Biosource International (Camarillo, CA) .
  • the human B cell lymphoma clone RAMOS 2G6.4CN 3F10 (Ramos 2G6) is available from ATCC. 293/CD8 is a human kidney tumor cell line that is stably transfected with CD8 as described (10,50) .
  • Stable CD40-L* clones of 293 cells (293/CD40-L) were generated by electroporation of a cDNA that encodes CD40-L (pCD40-L/SpeI) and cloning of transfectants that express surface CD40-L by mAb 5c8 binding.
  • pCD40-L/SpeI a CD40-L cDNA (pTBAM described in Covey et al .
  • the 3' oligonucleotide corresponds to pCCD40-L 616-633 (oCD40-
  • L 6 __- 616 5 ' ⁇ CTT TAG GCA GAG GCT GGC-3' ) ( Seq I.D. No. ) .
  • the PCR product generated was digested with Nhe I and Hind III, cloned into the expression vector pREP4 (Invitrogen, San Diego, CA) and its sequence was confirmed by automated sequencing.
  • the CD40-L coding region was completed by insertion of the 3' end of the pTBAM cDNA as a Hind III -Wot J fragment from pCCD40-L, yielding pCD40-L/SpeI .
  • Tonsil B cells were obtained from fresh surgical specimens after tonsillectomy.
  • the lymphoid tissue B cells were obtained by mincing tissue specimens and passing them through a metal screen followed by ficoll- hypaque (Sigma, St. Louis, MO) centrifugation.
  • B cells were derived from the population of cells that did not pellet through Ficoll-Hypaque after one round of rosetting with neuraminidase-treated sheep erythrocytes.
  • Tonsillar B cells were further purified by density centrifugation. Cells were fractionated into high (resting) and low (germinal center CD38 enriched) density cells in a discontinuous 30%/50%/100% percoll gradient by centrifugation at 2300 rpm for 12 min. High density cells were obtained from the 50%/100% interface and low density cells from the 30%/50% interface (33 , 51) .
  • Ramos B cells (3 X 10 6 ) or freshly isolated low density or high density tonsillar B cells (5 X 10 6 ) were added to each well of sterile 12 well tissue culture plates
  • mAb W6/32 0.5 ⁇ g/ml anti-CD95 mAb (APO-l/huFc ⁇ l) or control chimeric anti-CD4 (mAb M-T412/huFc ⁇ l) , 5 ⁇ g/ml anti-IgM or 5 ⁇ g/ml or 0.5 ⁇ g/ml of control anti-Class I (mAb W6/32) as indicated in figure legends.
  • wells contained either media, 0.5 X 10 6 TBAM/293 cells or CD8/293 cells in the presence or absence of mAbs anti- CD40-L (5c8) or control mAb (W6/32) in a final volume of 1 or 2 ml.
  • Cultures were incubated for either lOh or 14h (anti-CD95 induced apoptosis) or 36 h (anti-IgM induced apoptosis) before cells were harvested and analyzed for apoptosis by cell morphology and DNA fragmentation into nucleosomal units.
  • DNA fragmentation was assessed by a modification of Benhamou et al. (53) .
  • Treated cells were washed twice in HBSS and lysed in 400 ⁇ l of buffer containing 10 mM EDTA, 200 mM NaCl, 0.1 mg/ml Proteinase K, 0.5% SDS, and 50 mM Tris-HCl (pH 8.0) . After lh incubation at 50° C, lysed cells were subjected to phenol-chloroform extraction. Genomic DNA was precipitated by the addition of 2 volumes of 100% ethanol and was removed using a sterile pipette tip.
  • Fragmented DNA was precipitated after the addition of 1/10 volume of 3 M NaOAc (pH 7.2) and incubation at -70° C for 2-5 h. Precipitated DNA was then washed with 70% ethanol, dried, and resuspended in 20 ⁇ l of RNase buffer consisting of 15 mM NaCl, 10 mM Tris-HCl (pH 7.5) and 5 ⁇ g/ml RNase A. After incubation at 50° C for 1 h, DNA was electrophoresed on a 1.5% agarose gel at 80 V for 1-
  • This method allows for the isolation of fragmented DNA only and therefore can be used to assess the relative level of apoptosis in the B cell population when total sample is loaded to each well, since each sample contains an equivalent number of tonsillar or Ramos B cells and 293 cells are resistant to CD95 induced apoptosis.
  • oligonucleotide primers used in these experiments are designated “o”, followed by “CR” for CRAFl, followed by “f” or “r” for forward and reverse respectively and then the nucleotides that they correspond to with the numbering of the CRAFl nucleotide sequence of clone IHb that is deposited in Genbank U21092) .
  • These oligos include: oCRf (127-144) (5' -AgC AgA ACg CTg Cgg ACC) (Seq. I.D. No. ) , oCRr(675-658) (5' -
  • oCRr(213-197) (5'-ggA AAg Agg AgT TCT Cg) (Seq.
  • RT-PCR The four overlapping cDNA fragments were amplified by RT-PCR in which the RT reaction was primed with oCRr (2119-2102) .
  • the following pairs were found to produce the expected products in RT-PCR on mRNA from a control EBV transformed B cell line: including (1.) oCRf (127-144) /oCRr(675-658) yields product (127-675) ,
  • the PCR product generated by oCRf (550-567) and oCRr (1091-1074) which yields product (550-1091) was cloned into pCRII (Invitrogen) and digested with Bgl II (which cuts within oCRf (550-567) ) and EcoRl (which cuts in the polylinker of pCR-II and generates similar fragments (except for the patient A or B sequence transitions) independently of the fact that the PCR products from A and B were initially cloned into pCRII in different orientations.
  • pCRII Invitrogen
  • Bgl II which cuts within oCRf (550-567)
  • EcoRl which cuts in the polylinker of pCR-II and generates similar fragments (except for the patient A or B sequence transitions) independently of the fact that the PCR products from A and B were initially cloned into pCRII in different orientations.
  • the Bglll/EcoRI fragments of patient cDNAs were ligated into pCRAFl/Bluescript digested with Bgl II/Eco RI to yield fragments that contain the premature termination codons of patient A and B.
  • the cDNAs encoding the full coding sequence of the patients were then digested with Not I/Xho I and ligated into pCEP/CRAFl and pEBV/His/CRAFl.
  • CRAF-1 Isoforms with Zinc Finger Deletions One isoform of CRAF-1 peptide is a 568 aa signaling protein that interacts with the cytoplasmic tail of B cell surface molecule CD40 and mediates a variety of T- dependent effects on B cell activation and differentiation.
  • CAP-1 which is a cDNA related to CRAF-1 nucleic acid, is similar to a CRAF-1 nucleic acid except for a 75 nucleotide deletion in a region which, in a CRAF-1 nucleic acid embodiment provided for herein, encodes five zinc finger-like domains.
  • CRAF-1 nucleic acid mRNA and genomic DNA were analyzed using RT-PCR (reverse transcriptase - PCR) and long-template PCR amplification, respectively, followed by subcloning and sequence analysis.
  • RT-PCR reverse transcriptase - PCR
  • CAP-1 del aa218-242
  • a third mRNA species was identified that predicts a peptide with a larger (52 aa) deletion in this region (del aal91-242) .
  • agents that drive such alternative splicing are expected to have beneficial effects similar to mAb 5c8 treatment (See U.S. Patent No. 5,474,771, issued December 12, 1995) .
  • Such agents include gene therapy constructs that encode elements of the splicing appratus. These constructs may be used singly or in combination. For example, certain elements of the splicing complex that have effects on RNA splicing generally, may be over-expressed alone, or in combinations with other elements of the splicing complex that has specific targeting effects on the CRAF-1 RNA splicing.
  • genes include both gene therapy constructs that encode protein elements of the splicing complex as well as others that encode RNA elements of the splicing complex.
  • Activity of gene therapy constructs comprising the whole proteins or whole RNA molecules that participate in RNA splicing allows the identification of smaller constructs containing minimal essential elements of these nucleotide segments, for example steroid-like molecules.
  • the identification of the minimal elements leads to the identification of smaller organic molecules that have the essential chemical features and biological activity of the larger DNA elements (enhancing the RNA splicing that generates CRAF-l isoforms by deleting a particular the RNA of a particular exon) .
  • Such agents include preferentially target the splicing of the particular exon which is removed.
  • Such agents include cytokines and small organic agents that induce cell differentiation or activation.
  • snRNAs small nuclear RNAs
  • Ul small nuclear RNAs
  • U2, U3, U4, U5 and U6 small nuclear RNAs
  • snRNPs small nuclear ribonucleoproteins
  • TRAF-3 (CRAF-1, LAP-1, CD40bp) is a cytoplasmic signaling molecule that interacts with the cytoplasmic tail of CD40 and transduces contact dependent signals for B cell activation.
  • the gene for TRAF-3 was characterized by FISH (fluorescence in situ hybridization) and by radiation hybrid mapping and found to be located at chromosome 14q32.2, approximately 1 Mbase centromeric to the Ig heavy chain locus.
  • TRAF-3 was further characterized by genomic PCR and sequencing genomic ⁇ -phage and PI clones.
  • TRAF-3 is encoded by 10 exons which roughly correspond to protein domains predicted by the TRAF-3 cDNA.
  • a variety of TRAF-3 cDNA species were identified which are generated by alternative mRNA splicing of distinct exons. Many of these species predict novel TRAF-3 peptides which vary in critical structural regions of this signaling protein.
  • TRAF-3 (CRAF-1, LAP1, CD40bp) is a 568 amino acid cytoplasmic signaling molecule that plays an important role in the transduction of signals from the CD40 receptor in B cells.
  • TRAF-3 has also been shown to bind the cytoplasmic domain of at least one other membrane receptor, the receptor for lymphotoxin- ⁇ , and TRAF-3 mRNA is expressed by cells of many lineages.
  • TRAF- 3 may also play a role in EBV-driven B cell proliferation and immortalization, by binding EBV latent membrane protein-1.
  • TRAF-3 is a member of the TNF ⁇ -receptor associated factor family "TRAF family" of signal transducing molecules on the basis of homology in the carboxy terminus of family members TRAF-1 and TRAF2. These signaling molecules contain a COOH-terminal TRAF subdomain (TRAF-C) that mediates protein:receptor binding.
  • TRAF-C COOH-terminal TRAF subdomain
  • sequence analysis of the TRAF-3 protein has revealed four other potential domains, including a zinc ring, a complex composed of five atypical zinc fingers, a coiled-coil (isoleucine zipper) structure, and an NH3-terminal (TRAF-N) domain.
  • zinc rings, zinc fingers, and coiled-coil structures mediate protein- protein interactions.
  • TRAF-3 isoforms
  • IHb TRAF-3 species
  • CAP- 1 Another species of TRAF-3 was reported by Reed, and termed CAP- 1, which predicts a peptide with a 25 aa deletion in the zinc finger complex.
  • TRAF-3 The chromosomal localization and genomic structure of TRAF-3 was determined, in order to understand the structure and genesis of TRAF-3 mRNA.
  • Various isoforms of TRAF-3 were identified which suggest that alternative splicing of TRAF-3 mRNA may generate distinct TRAF-3 peptides. Such isoforms may play different roles in the signaling function of TRAF-3, and may thus represent a mechanism for the regulation of TRAF-3 in B cells.
  • FISH fluorescence in situ hybridization
  • this region is known to contain the human immunoglobulin heavy chain locus, and since this locus contains a well-characterized breakpoint in Ramos cells, a non-EBV infected Burkitt's tumor cell line, localization of TRAF-3 with respect to this chromosomal landmark was performed.
  • Two-color FISH was performed on metaphase chromosomes from Ramos cells using the TRAF-3 probe and a chromosome 14 telomere probe. The two probes bound in very close proximity on the normal chromatid, within an estimated distance of 1 Mb.
  • TRAF-3 gene is located centromeric to the Ramos breakpoint on 14q32.
  • the close physical proximity of the two probes further suggested that TRAF-3 and this breakpoint, [which is within the C ⁇ switch region in the immunoglobulin heavy chain locus] are located within one Mb of each other, an estimate that was confirmed by a PCR-based screening assay of a somatic cell hybrid panel. From this screen, the TRAF-3 locus lies within 3.5 cR (approximately 1 Mb) of framework markers FB19F11 and WI-9179 on the Whitehead radiation hybrid database.
  • a Raji cDNA library was screened with C26, a cDNA probe that represents the terminal 1271 nt of the TRAF-3 open reading frame.
  • a second screen was performed with Notl- SacI, a probe which represents the first 447 bp of IHb.
  • exon contains a stop codon in the reading fram of exon 4 which contains the p55 translational start site (IHb nt 224; Figures 1A-1P, nucleotide 679) .
  • Another clone, 2-1 contained exon 3, and a third unique exon, at least 77 bp long, which precedes exon 3, and was called the product of exon 1.
  • RT-PCR for example, revealed the appropriate products encoding IHb-like, lb-like and 2-1-like species.
  • 5'- RACE Rapid Amplification of cDNA Ends
  • PI human genomic phage library
  • pAC clones three clones (#4, #6, and #9) that hybridized with cDNA probe Hindi-Hindi (IHb 606-1003) were isolated. These clones were characterized by restriction digestion with [Notl and EcoRI] and by PCR mapping. Each phage clone contained an insert of about 20 kb. Two of these clones (#4 and #9) were found to be overlapping but distinct, containing the 3' end of the gene [nt 981-2437 on IHb cDNA] ; the third clone, #6, was found to encode the 5' end of the gene [nt 207-793 on IHb cDNA] . The gap from nt 794-981 is covered by pAC clone #167.
  • TRAF-3 To further characterize the genomic structure of TRAF-3, a human genomic PI (or pAC) artificial chromosome library was screened with two different TRAF-3 genomic probes, ff7gen-fr8gen and pstlc-r2glx.
  • the TRAF-3 5'-UTR was not contained on the most 5' ⁇ -fix clone (clone #6) or on PI clone #167 by Southern blotting with probe CE, a 193 bp fragment which contains part of the TRAF-3 5'-UTR including exon 3. Therefore, the genomic library was re-screened with this probe, and a single PI clone [#34] (pAC clone #34, ATCC Accession No. ) was isolated. Restriction digestion of
  • PI clone #34 with EcoRI identified a 3.8 kb genomic restriction fragment that hybridized to the CE probe. Furthermore, a 6.0 kb EcoRI fragment was identified that hybridized to zfl, a 25 bp end-labeled oligonucleotide primer that represents part of exon 1. A third EcoRI fragment, 7.0 kb long, hybridized to probe Notl-Smal, which represents the 5' half of exon 2. All three genomic fragments were subcloned into Bluescript and sequenced in both directions, using exon-specific primers, confirming these data.
  • the CRAF exons were flanked on the 5' -side of ;AC #34 by ORF (D14S72) and on the 3' -side of pAC #167 by EST (SGC 30775) , confirming the chromosomal location determined by FISH and radiation hybrid mapping and which indicated that pAC #34 is centromeric to pAC #167 and that the transcriptional orientation of the CRAFl gene is centromeric to telomeric, or in the reverse orientation of the Ig heavy chain gene locus (transcriptional orientations are indicated by arrows in Figure 6.
  • genomic clones ⁇ fix clones #6 and #9 and pAC clones #167 and #34 were sequenced in both directions using oligonucleotide primers developed from TRAF-3 cDNA clones lb, IHb, and 2-1 [Tables 1 and 3] . Comparison between genomic and cDNA sequence data permitted the definition of exon/intron boundaries for each of the TRAF-3 (p55) coding exons as well as the 3' borders of exons 1, 2 and 3. The 3' border of exon 1 was determined from the spliced species which represented an exon 1,3 product.
  • PCR was performed on both control human genomic DNA and on ⁇ -phage and PI genomic clones. Oligonucleotide primer pairs spanning each of 9 consecutive coding exon/intron junctions were developed from the IHb cDNA sequence. These were used to amplify genomic human DNA.
  • the resulting PCR products consisting of an intron bordered by two adjacent exon fragments, were sequenced to confirm their identity.
  • the nine introns identified in this way ranged in size from 600 bp to 9.5 kb [Table 3] .
  • RT-PCR amplification of human TRAF-3 mRNA from these five donors revealed subtle length variations in cDNAs amplified from two regions of TRAF-3: the 5'-UTR and the zinc finger region. In all cases examined these length variations corresponded to the alternative splicing of specific TRAF-3 exons.
  • TRAF-3 sequence The second was a 687 bp fragment, which was detected in three of the four subjects studied
  • TRAF-3 is a single copy gene located on chromosome 14q32.2. This region plays a major role in B cell development as the immunoglobulin heavy chain switch region, which normally undergoes germline rearrangements during B cell development, and which is frequently involved in various translocations in certain hematologic diseases. It is therefore possible and even likely that the expression of TRAF-3 is regulated by the genomic splicing that takes place at this locus during normal B cell development, or is dysregulated by translocations. What the results of such events might be are difficult to predict. It may be for example, that normal rearrangements regulate expression of TRAF-3 by inactivating one allele, or that TRAF-3 is upregulated or, like bcr-abl , fused with other gene products during rearrangement or translocation.
  • TRAF-3 may play a role in identifying that subset of HIGM patients who have a TRAF-3 defect. While the essential roles of CD40-L and CD40 in the phenotype of HIGM syndrome has been confirmed by targeted disruption of either CD40-L or CD40 in mice, no such evidence has yet been found for that subset of non-X-linked HIGM patients. Determination of defects in TRAF-3 may mediate immune deficiency syndromes with the HIGM phenotype. A subset of individuals with HIGM syndrome have normal CD40-L.
  • TRAF-3 may be linked with other genes that are associated with human diseases.
  • a form of HIGM with normal CD40-L was described that is associated with hypohidrotic ectoder al dysplasia, but in this family the syndrome appears to be inherited in an X-linked pattern and therefore may represent a different form of non-CD40-L HIGM.
  • the chromosomal localization of TRAF-3 will be of interest, therefore, in identifying this and related syndromes.
  • TRAF-3 p55 is encoded by 10 exons (exons 4-13), which correspond roughly to protein domains predicted by the TRAF-3 cDNA sequence.
  • exons 4 and 5 encode the zinc ring
  • exons 6-10 encode the zinc finger complex
  • exon 11 and the NH2- terminal encoding half of exon 12 encode the helical wheel
  • the remaining half of 12 and 13 encode the N- TRAF domain and the TRAF-C domain is encoded by exon 13.
  • exon 13 Such structural detail is of general interest, as none of the TRAF family members have until now been analyzed at this level, and given their homology and similar functions, they presumably all have similar exonic arrangements.
  • TRAF-3 which appears to be regulated by alternative splicing.
  • TRAF-2 which also has a multi-zinc finger domain, appears to undergo similar splicing.
  • the zinc finger complex consists of a single large exon, which encodes the 5' half of this region followed by three smaller exons, which encode the remaining zinc fingers.
  • the organization described here suggests that the TRAF-3 zinc finger complex has evolved by the duplication of an original progenitor exon, leading to the addition of successive zinc fingers.
  • a comparative amino acid analysis of TRAF-3 in the zinc finger complex shows that the in the 3' half of this domain there is 100% identity between murine and human sequences.
  • seven of the 80 preceding amino acids that make up the 5' half of this complex are divergent, and four of these seven changes are non- conservative.
  • Such conservation in the 3' part of this complex implies that this portion of the zinc finger complex is significant in the signaling function of TRAF-3.
  • each isoform encodes a different combination of zinc fingers in the 3' half of this complex. This interchangability of exons is made possible by their common coding class, which ensures that removal or insertion of a given exon will not affect reading frame [Table 3] .
  • the possible consequences of such splicing are intriguing, in that zinc fingers commonly mediate both protein-protein and protein-DNA interactions.
  • Each of these isoforms may interact with separate constituents of the cytoplasmic signaling apparatus, for example.
  • exons 1,2,4-13 evidence for the alternative use of exons has not been limited to the TRAF-3 coding sequence, but was initially revealed in the 5'-UTR, through variation among cDNA clones in exons 2, 3, and 4-13. The significance of this phenomenon (which is quite common, at least with respect to exon 3) , is uncertain. It should be noted, however, that the IHb form of TRAF-3 contains an open reading frame which precedes the initiating methionine at IHb nt positio 224. Interestingly, exon 2 is in frame with the rest of TRAF-3. Thus, while the inclusion of exon 3 leads to an early stop in translation, its removal allows for the production of a longer TRAF-3 species, exons 1,2,4-13.
  • p55 could be encoded by the gene described herein, due to alternative promoters, alternative transcription initiation, alternative translation initiation or internal ribosomal re-entry.
  • promoters e.g., c-able gene (Bernards, A., et al . 1988. Oncogene 2:297)
  • c-able gene Boet al . 1988. Oncogene 2:297
  • an undetected promoter exists in the 1-2 intron
  • such a promoter may be a "TATA-less" promoter (Smale, S. T. and
  • Bloom syndrome gene (e.g., Bloom syndrome gene (Ellis, N. A., et al. 1995.
  • Each isoform may play a role in modulating signaling mediated by TRAF-3.
  • Each isoform may participate in a different signaling pathway, and may have a different level of expression or activity in a given cell. Some forms may act to inhibit others, or may be present only at critical moments in cellular development. The over-expression of these isoforms, therefore, in various cell lines may reveal important functional differences between them.
  • a ⁇ -gtll Raji cDNA library (Stratagene) was screened. Probed with a 5' probe: Notl-SacI and with a 3' probe: C26. Clones were isolated by plating phage according to standard procedures on lawns of E. coli and plaque purified.
  • a human genomic ⁇ -fix library (Stratagene) was screened. Clones were isolated by plating phage according to standard procedures on lawns of E. coli (P2932) and plaque purified. A human genomic 3.5x arrayed PI artificial chromosome library was used. Average insert size is 100 kb. This was prepared by partial Sau3AI digest and ligated into PCYPAC2. The library was screened with CRAFl specific probes. Clones were isolated by transforming E.
  • DH10B DH10B
  • printing colonies (6144 colonies/filter) onto high density nylon membranes SureBlot, Oncor
  • Biomek 2000 Automated Laboratory Workstation equipped with a high density replicating system (Beckman)
  • processing filters as described by Olsen et al .
  • IHb IHb 1-2467) a 2.4 kb cDNA which contains exon 2 as well as the entire TRAF-3 open reading frame.
  • Notl-S al IHb nt 26-128) , a 102 bp restriction fragment which contains the 5' half of exon 2.
  • NotI-Sad a probe which represents the first 447 bp of IHb.
  • CE lb nt 12-205
  • a 193 bp probe derived from cDNA clone lb which represents a part of the TRAF-3 5'-UTR and contains exon E.
  • Hindi-Hindi IHb 606-1003
  • zfl 2-1 nt 158-82)
  • tggcaaactggctaccctgtccacc Seq I.D. No. is a carboxy-terminal oligonucleotide fragment of exon 1.
  • ff7gen-fr8gen is a 4.1 kb genomic fragment generated by genomic PCR using primers ff7gen and fr ⁇ gen (Table 3) which spans exons 5 and 6.
  • pstlc-r2glx is a 5.8 kb genomic fragment generated by genomic PCR using primers pstlc and r2glx which spans exons 8 to 10.
  • ⁇ phage genomic clones were sequenced on an automated DNA sequencer (ABI) using 5.0 ⁇ g per sequencing reaction.
  • PI clones were sequenced manually by cycle sequencing (Gibco Cycle Sequencing kit) using 1.5 ⁇ g template DNA under the following conditions: DNA initial denaturation 95 °C 3 min; denaturation 95 °C 30 sec, annealing 64 °C 30 sec, extension 70 °C 60 sec X 20 cycles; denaturation 95 °C 30 sec, extension 70 °C 60 sec X 15 cycles.
  • Genomic PCR was carried out using the Expand long template PCR kit (Boehringer-Mannheim) as per the manufacturers directions. Human genomic DNA was extracted from Ramos cells as follows: 50 x 10 6 cells pelleted lx and washed 2x in PBS 5 min at 500 G, resuspended in 0.5 ml digestion buffer (100 mM NaCl, 10 mM TrisCl pH 8.0, 25 mM EDTA pH 8.0, 0.5% SDS, 0.1 mg/ml proteinase K) , incubated with gentle shaking at 50 °C 18 hrs, phenol-chloroform extracted 3x, and dialyzed against TE 24 hrs (Current Protocols 2.2, Ausubel et al .
  • RT-PCR of the zinc-finger complex and the 5'-UTR regions were performed as follows. HIGM patients A and C, and C's unaffected mother CM were used. Patient B and an unaffected mother of another HIGM patient, RS, were provided. Total RNA was extracted (RNeasy kit: Qiagen) from EBV-immortalized human B cell lines from all five donors. RNA was oligo-dT primed and reverse transcribed into cDNA (Superscript II, Gibco BRL) . cDNA was amplified by PCR in the 5'-UTR using primers df7 (IHb nt 133-150) agcagaacgctgcggacc (Seq. I.D. No. ) and fr ⁇ (IHb nt 681-664) cagtcaggacgcacacat (Seq. I.D.
  • RT-PCR products were separated by agarose gel electrophoresis and visualized by staining with ethidium bromide.
  • RT- PCR products were gel purified and ligated into pCR2.0 and 2.1 (Invitrogen) . Ligation products were cloned in E. coli and clones were examined for insert.
  • CRAFl peptide Despite wide tissue distribution CRAFl peptide appears to have distinct and essential role in contact-help. CD40 is broadly expressed in many types of cells. CRAFl peptide is ubiquitously expressed. Targeted gene disruption of CRAFl nucleic acid results in defective contact-dependent helper function. Despite "collateral" signaling pathways, CRAFl peptide is essential for T helper function. Analysis of CRAFl nucleic acid mRNA revealed alternative mRNA splicing. A variety of CRAFl nucleic acid mRNA species were isolated. A variety of splicing events alters the number of zinc-finger like domains. The three CRAFl peptide isoforms are predicted by cDNA encoding loss of Zn-finger encoding exons.
  • the IHb type species (with an appended amino terminal peptide domain) is expressed by activated B cells and fibroblasts by RT-PCR.
  • Hyper IgM patients with normal CD40-L preferentially express p70.
  • Two unrelated HIGM patients expressed abnormal ratio of p70 and p60 mRNA.
  • HIGM patients may overexpress p70 encoding mRNA. They may lack an in fram stop codon in exon 3.
  • CRAFl peptide and variants thereof and isoforms thereof combined with carriers or therapeutically acceptable agents for delivery may be used as therapeutic compositions or therapeutic pharmaceuticals for administration to subjects.
  • Dominant negative CRAFl peptide may be used in gene therapy as immunomodulator or i munosuppressive therapeutics. Such peptides may be co-administered with other therapeutic genes.
  • Peptide minmetics or small molecules are examples of agents which may be used to mimic inhibitory CRAFl peptides. Screening would be facilitated by identification of p70 interacting species by systems such as the two-hybrid yeast system.
  • Genomic sequencing has been done using the genomic clones as described in Figures 7A-7B, 8 and 9A-9C.
  • Numbering is based on clone Illb which is deposited in the GenomeBank.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Molecular Biology (AREA)
  • Hematology (AREA)
  • Cell Biology (AREA)
  • Urology & Nephrology (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Pathology (AREA)
  • General Physics & Mathematics (AREA)
  • Physics & Mathematics (AREA)
  • Food Science & Technology (AREA)
  • Zoology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Toxicology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Virology (AREA)
  • Genetics & Genomics (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Biophysics (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

The present invention provides an isolated CRAF1 peptide encoded by the nucleic acid sequence shown from base 169 to base 2381 of Figures 1A-1P or a variant thereof. One embodiment of the present invention is an isoform of the CRAF1 peptide. The present invention also provides for a method of inhibiting activation by CD40 ligand of cells expressing CD40 on the cell surface, comprising providing the cells with the CRAF1 peptide or variant thereof, the peptide being present in an amount effective to inhibit activation of the cells. The present invention further provides for a method of treating a condition characterized by an aberrant or unwanted level of CD40-mediated intracellular signalling, in a subject, comprising providing the subject with a therapeutically effective amount of a peptide of this invention capable of inhibiting CD40-mediated intracellular signalling in cells bearing CD40 on the cell surface.

Description

CRAFl (TRAF-3) ISOFORMS AND USES THEROF
This application claims the benefit of U.S. Provisional No. 60/013,820, filed March 21, 1996; U.S. Provisional No. 60/026,584, filed September 18, 1996; U.S. Provisional No. 60/016,659, filed May 1, 1996; and U.S. Provisional No. 60/016,626, filed May 1, 1996, the contents of which are hereby incorporated by reference into the present application.
The invention disclosed herein was made with Government support under NIH Grant No. R01-CA55713 from the Department of Health and Human Services. Accordingly, the U.S. Government has certain rights in this invention.
Throughout this application, various references are referred to in the text within parentheses in full or within parentheses by number. Disclosures of these publications in their entireties are hereby incorporated by reference into this application to more fully describe the state of the art to which this invention pertains. Full bibliographic citation for those references referred to by number may be found at the end of this application, preceding the claims.
The following standard abbreviations are used throughout
Figure imgf000003_0001
Figure imgf000003_0002
Background of the Invention
CD40 (1) is a receptor on B cells that interacts with the helper T cell surface protein CD40L (CD40 ligand, also known as T-BAM, gp39, or TRAP) (2-4) . CD40L is found particularly on lymphoid follicle CD4+ T lymphocytes, where it delivers a contact-dependent signal that stimulates B cell survival, growth, and differentiation (2-4) . Signaling through CD40 rescues B cells from apoptosis induced by Fas (CD95) or by cross-linking of the immunoglobulin M (IgM) complex (5) ; it also induces B cells to differentiate and to undergo Ig isotype switching (3) and to express CD80 (B7 or BB- 1) (6) . The crucial role of CD40L-CD40 interaction is illustrated by humans with defects in CD40L, who manifest a serious immune deficiency syndrome, the X- linked hyper-IgM syndrome (HIGMX-1) characterized by an absence of IgG, IgA, and IgE, elevated IgM, and no lymphoid follicles (7) . The essential roles of CD40L and CD40 in the phenotype of HIGMX-1 syndrome has been confirmed by targeted disruption of either CD40L (8) or CD40 (9) in mice. In addition to B cells, CD40 is also expressed by follicular dendritic cells (10) , dendritic cells (11) , activated macrophages (12) , epithelial cells (including thymic epithelium) (13), and a variety of tumor cells.
Stimulation of CD40 causes the tyrosine phosphorylation of multiple substrates including Src family kinases such as p53-p56lyn, activates multiple serine-threonine- specific protein kinases, and induces the phosphorylation of phospholipase C-γ2 and of phosphoinositol-3' kinase (14) . CD40 ligation also stimulates protein kinase C-independent activation of the mitgen-activated protein kinases (MAPK) family, including the extracellular signal-regulated protein kinases 1 and 2 (ERK) and the c-Jun NH2-terminal kinases (JNK isofor s) (Li, Y. et al . (1996) J. Immunol. 157:1440) . In mice the CD40 cytoplasmic tail is necessary for signaling (15) . Proteins which interact with the cytoplasmic tail of CD40 have been described (H.M. Hu, et al., J. Biol . Chem. 269: 30069 (1994); and G. Mosialos, et al. , Cell 80:389 (1995)) . These proteins are the same as CRAFl .
CD40 signaling is known to be complex and may be mediated or modulated by TRAF-2 (Rothe, M. et al . (1995)
Science 269:1424), TRAF-5 (Nakano, H. (1996) J. Biol.
Chem. 271:14661) and TANK (Cheng, G. And Baltimore, D.
(1996) Genes Dev. 10:963; Rothe, M. et al . (1996) PNAS
USA 93:8241) either alone or in interactions with TRAF- 3. TRAF-2 signals may be modulated by TANK (or I-TRAF)
(Rothe, M. et al. (1996) PNAS USA 93:8241) or by A20, a
TNFa-induced gene product (Song, H.Y. et al. (1996) PNAS
USA 93:6721) .
Summary of the Invention
The present invention provides an isolated CRAFl peptide encoded by the nucleic acid sequence shown from base 169 to base 2381 of Figures 1A-1P or a variant thereof. One embodiment of the present invention is an isoform of the CRAFl peptide. The present invention also provides for a method of inhibiting activation by CD40 ligand of cells expressing CD40 on the cell surface, comprising providing the cells with the CRAFl peptide or variant thereof, the peptide being present in an amount effective to inhibit activation of the cells. The present invention further provides for a method of treating a condition characterized by an aberrant or unwanted level of CD40-mediated intracellular signaling, in a subject, comprising providing the subject with a therapeutically effective amount of a peptide of this invention capable of inhibiting CD40-mediated intracellular signaling in cells bearing CD40 on the cell surface.
Description of the Figures
Figures 1A-1P. Sequence of TRAF-3 (CRAF-1) and Isoforms thereof. Sequence data of CRAFl is shown including cDNA sequence of isoforms of CRAFl including CRAFl-a (p55; p60 isoform) , CRAFl-b (p70; p77 isoform), smaller CRAFl pre-peptides (p5 isoform and pl5 isoform) , and other deletion isoforms and alternative splice possibilities. The DNA and amino acid sequences of such isoforms are also indicated. The base pair number and the amino acid residue number are indicated.
Figures 2A-2B. Fig. 2A. Schematic diagram of the genomic structure of the zinc finger region of CRAF-1. Fig 2B. Schematic diagram of the cDNA structure of the zinc finger regions of CRAF-1, CRAF-1 (del aa 218-242) , and CRAF-1 (del aa 191-242) , as indicated. Predicted amino acid sequences of human CRAFl-a (residues 1-568) .
Figure 3. Exon Organization, Numbering and Arrangement in TRAF-3 cDNAs.
Figure 4. Predicted CRAFl zinc fingers, corresponding to residues 110 to 264. The zinc fingers are numbered consecutively from 1 to 5, proceeding from the amino terminus to the carboxy terminus . The numbering of the amino acids is based on the sequence shown in Figures 1A-1P, in which the initial "M" residue is +1.
Figure 5. Differential expression of CRAFl isoforms in hyper-IgM patients. Western blot analysis. Cell lysates from 1 x 107 cells of B cell tumor lines (lanes 1-7 non- transformed, 8-12 EBV-transformed) were immunoprecipitated with a rabbit antiserum directed against TRAF-3 (CRAF-1) molecule. Following the SDS- PAGE, the proteins were transferred to a nitrocellulose sheet and probed with the anti-CRAF-1 antiserum. The specificity of this antiserum is demonstrated by the fact that the low molecular weight CRAF-1, p60 CRAF,
(lanes 1-4, 6-10, and 12) can be specifically inhibited by a synthetic peptide (corresponding to the N-terminal 22 amino acid residues of CRAF-1) which was used as the imrnunogen to generate the rabbit anti-CRAF-1 antiserum
(lane 5) . The 55 kDa component found in every lane is the immunoglobulin heavy chain (IgH-chain) . BJAB (tx
CD40) is BJAB transfected with CD40 and overexpressing CD40. RCC/CRAF is Ramos CC transfected with and stably expressing a cDNA construct encoding CRAFl-a (TRAF-3- p70) , and overexpressing CRAFl-a mRNA. BL41 is a B cell tumor cell line.
The expression of the p60 CRAF-1 is comparable in all the cell lines examined except the EBV-transformed B cells from patient B, in which only trace amounts of the p60 CRAFl was detected. This result shows that p60 CRAFl is normally expressed in B lymphocytes.
A high molecular weight CRAFl, p70 CRAF (TRAF-3-p70) , was identified in EBV-transformed B cells (lanes 9-12) , but not in non-EBV-transformed cell lines. However the expression level of p70 CRAFl varies. In EBV- transformed B cells established from normal B lymphocytes, p70 CRAF is only expressed at low levels
(lane 9) . However, in EBV-transformed B cells from patient A, the expression of p60 CRAF and p70 CRAFl is comparable (lane 10) . Moreover, in EBV-transformed B cells from patient B, the expression of p70 CRAFl is not only dominant but also dramatically up-regulated and only trace amounts, of the p60 CRAFl was detected in these cells (lane 11) . In contrast to the hyper IgM patients A and B (which are known to have normal CD40L) in EBV-transformed cells established from patient C, the p70 CRAFl expression is below the level of detection (lane 12) . Figure 6. Genomic localization and Orientation of the human TRAF-3 Gene on 14q32.
Figures 7A-7B. The Entire TRAF-3 Gene is Encoded on Two pAC clones. A schematic of two pAC clones is illustrated along with peptide-encoding regions.
Figure 8. Complexity of CD40/p80/LT-βR Interactions with TRAF-3, TRAF-1 and TRAF-2.
Figures 9A-9C. Relationship of CRAFl/TRAF-3 Isoforms to Truncated C26 clone and peptide domains.
Figures 10A-10D. 5' -Untranslated Region of Human TRAF-3 Gene with Transcription Regulatory Functions
Detailed Description
This invention provides for an isolated CRAFl peptide encoded by the nucleic acid sequence shown from base 169 to base 2381 of Figures 1A-1P or a variant thereof.
The CRAFl peptide may be an isoform of the CRAFl peptide. The isoform may comprise a p5 peptide, a pi5 peptide, a p55del9 peptide, a p70del9 peptide, a p55del9,10 peptide, a p70del9,10 peptide, a p55del-8,9 peptide, a p70del-8,9 peptide as shown in Figures 1A-1P.
The CRAFl peptide may comprise from zero to four zinc finger domains; wherein when the isoform comprises zinc finger domain 1, 2 and 5, the peptide further comprises one or both of zinc finger domains 3 and 4. The isoform may comprise a CRAFl peptide or variant thereof comprising zero, one, two or four zinc finger domains. The peptide may have deleted zinc finger domains 2, 3 and 4. The peptide may have deleted amino acids 191 to 242 or amino acids 313 to 364 as shown in Figures 1A-1P.
The peptide may comprise the sequence GARRGRRVREPGLQPSRDFPAGGSRGGRRLFPAPRHGAARGA(E/K) (R/C) CG PRR(Q/R)TRPAPLSRPSGDGP(Q/R)ELLFPK (Seq I.D. No. ) or a variant thereof capable of inhibiting CD40-mediated cell activation.
The isoform may have a molecular weight of about 5 kDa or about 15 kDa.
As used herein "CRAFl" is also termed "TRAF-3" . CRAFl nucleic acid encompasses the nucleic acid sequence shown in Figures 1A-1P. "CRAFl-a" is also termed "TRAF-3-p55" or "p55" or "CRAFl (p55)" or "TRAF-3 (p55)" or "CRAFl (p60) ". "CRAFl-b" is also termed "TRAF-3-p70" or "p70" or "CRAFl (p70)" or "TRAF-3 (p 70)". p60 is also termed p55 (p60 = p55) and p77 is also termed p70 (p70 = p77) . "P70-i" as used herein encompasses all of the isoforms of p70. and p70-i is represented in Figures 1A-1P as the longest isoform of p70.
As used herein, "CRAFl gene" encompasses a nucleic acid sequence comprising a genomic sequence of a CRAFl nucleic acid. Two embodiments of a CRAFl gene are the sequences contained in the two pAC clone nucleic acid constructs (pAC clone number 34 and pAC clone number 167) which have been deposited on March 21, 1997 with the American Type Tissue Culture Collection (ATCC) , 12301 Parklawn Drive, Rockville, Maryland 20852, U.S.A. under the provisions of the Budapest Treaty for the International Recognition of the Deposit of Microorganism for the Purposes of Patent Procedure. pAC clone no. 34 was accorded ATCC Accession No. and pAC clone no. 167 (PI artificial chromosome 167) was accorded ATCC Accession No. . Another embodiment of a CRAFl gene is the human CRAFl gene. A portion of the human CRAFl gene is shown in Figures 1A- 1P from nucleotide numbers 1-2918. Other embodiments of the present invention provide for the homologous murine CRAFl gene, and the analogous homolog CRAFl gene in other species of animals. Further embodiments of a CRAFl gene are the sequences contained in the following deposits: pE, pGM and pZAC which have been deposited on March 21, 1997 with the American Type Tissue Culture Collection (ATCC) , 12301 Parklawn Drive, Rockville, Maryland 20852, U.S.A. under the provisions of the Budapest Treaty for the International Recognition of the Deposit of Microorganism for the Purposes of Patent Procedure. pE was accorded ATCC Accession No. and pGM was was accorded ATCC Accession No. and PZAC was accorded ATCC Accession No. As used herein, "CRAFl nucleic acid" encompasses the DNA nucleic acid sequence shown in Figures 1A-1P from (169- 2381) which encodes CRAFl (p70) or p70-i as designated in Figures 1A-1P. One embodiment of the present invention is CRAFl nucleic acid comprising DNA, recombinant DNA, cDNA, mRNA or RNA. Another embodiment of the present invention is the reverse complement of CRAFl nucleic acid. A further embodiment of the present invention is a nucleic acid molecule comprising at least a portion of the CRAFl nucleic acid sequence shown in Figures 1A-1P in an antisense orientation. The nucleic acid may be an isolated nucleic acid or a purified nucleic acid which nucleic acid is separated from cellular particles substantially. Such isolation or purification would be known to one of skill in the art, see Sambrook, et al. Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press, Cold Spring Harbor, New York (1989) .
One embodiement of this invention is a nucleic acid comprising of a portion of the human CRAFl nucleic acid sequence shown in Figures 1A-1P. Such embodiments may be isoforms (p70-i) of the CRAFl nucleic acid such as deletion mutants, insertion mutants or substitution mutants, wherein portions of the nucleic acid sequence is deleted, inserted or substituted, respectively. Examples of such isoforms are indicated in Figures 1A- 1P, i.e. p5, pl5, p55-l, etc. Further embodiments of this invention are described in Tables 1 and 2 (see Experimental Details section hereinbelow) . /Another embodiment of the present invention is the deposited cDNA clone IHb, ATCC No. 97489. A further embodiment of the present invention are pAC clones which encompass the entire CRAFl genomic sequence or a portion of the CRAFl genomic sequence.
This invention provides for a nucleic acid comprising - li ¬ the cDNA nucleotide sequence of human CRAFl IHb clone (TRAF-3 (p55) ) which was deposited in GenBank with accession number U21092. This plasmid, pBluescriptSKII+/IIIb, was deposited on March 21, 1996 with the American Type Culture Collection (ATCC) , 12301 Parklawn Drive, Rockville, Maryland 20852, U.S.A. under the provisions of the Budapest Treaty for the International Recognition of the Deposit of Microorganism for the Purposes of Patent Procedure. Plasmid pBluescriptSKII+/IIIb was accorded ATCC Accession Number 97489.
This invention provides for alleles of the CRAFl nucleic acid. This invention provides for human CRAFl nucleic acid (as shown in Figures 1A-1P) and also provides for the homologous murine CRAFl nucleic acid, as well as the homologous CRAFl nucleic acids in other species of animals.
The present invention also provides for upstream and downstream regulatory nucleic acid sequences of CRAFl nucleic acid. One embodiment of this invention is shown in Figures 1A-1P from nucleotides 1-168. Another embodiment of the present invention is shown in Figures 1A-1P from nucleotide 2382-2918. Another embodiment of the invention is shown in Figures 2A-2B which shows the 5' untranslated region of human TRAF-3 gene (CRAFl gene) with has been shown to function as a transcriptional regulator or modulator. This upstream sequence capable of being activated to increase expression of a gene (e.g. transactivated) by EBV infection. This sequence and variants thereof may be useful the modulation and/or expression of heterologous genes as part of recombinant, heterologous nucleic acid constructs. Such constructs may be used in gene therapy as described in more detail hereinbelow. The present invention also provides for nucleic acid probes derived from the nucleic acid sequence as shown in Figures 1A-1P and in Tables 1-4. Such probes may be useful in diagnostic testing of subjects for disease states and for determination of levels of CRAFl peptide expression or lack thereof . Such probes may have other uses such as a monitor use in gene therapy or alternative therapy of subjects suffering from a CRAFl related disorder.
The present invention also provides for a CRAFl nucleic acid molecule linked to a vector. The vector may be a self-replicating vector or a replicative incompetent vector. The vector may be a pharmaceutically acceptable vector for methods of gene therapy. An example of replication incompetent vector is LNL6 (Miller, A.D. et al. (1989) BioTechniques 7:980-990) .
The present invention provides for CRAFl nucleic acid which is produced by polymerase chain reaction (PCR) . An isolated CRAFl nucleic acid may be isolated by using PCR. Such reactions are well known to one of skill in the art. [U.S. Patent Nos. 4,754,065; 4,800,159;; 4,683,195 and 4,683,202 provide PCR techniques and methods and these U.S. Patents are hereby incorporated by reference in their entirties.]
As used herein, "CRAFl peptide" encompasses the amino acid sequence shown in Figures 1A-1P encoded by the nucleotide sequence from base 169 to base 2831 (therein termed p70-i) . CRAFl peptide is also termed TRAF-3 peptide (TRAF-3-p55 or CRAFl(p70)) .
This invention encompasses isoforms of the CRAFl peptide, the sequence of several of which are shown in
Figures 1A-1P, i.e. p5, pl5, p55-i, p55del-9, etc. Such embodiments and further embodiments of isoforms of the CRAFl peptide are described in Tables 1 and 2. Embodiments of CRAFl peptide include peptides produced from alternatively spliced transcripts derived from a CRAFl nucleic acid, CRAFl peptide isoforms with reduced numbers of zinc finger regions, truncated CRAFl peptide. Another embodiment of the present invention is a prematurely terminated CRAFl peptide, e.g. p5 and pl5 as shown in Figures 1A-1P and on Tables 1 and 2.
In another embodiment of the present invention CRAFl nucleic acid may also be a synthetic nucleic acid or a mimetic of a nucleic acid which may have increased bioavailability, stability, potency or decreased toxicity. Such synthetic nucleic acids may have alterations of the basic A, T, C or G or U bases or sugars which make up the nucleotide polymer to as to alter the effect of the nucleic acid.
This invention provides an isolated protein comprising a CRAFl peptide (TRAF-3-p70) domain which comprises
GARRGRRVREPGLQPSRDFPAGGSRGGRRLFPAPRHGAARGA(E/K) (R/C) CG
PRR(Q/R)TRPAPLSRPSGDGP(Q/R)ELLFPK (Seq I.D. No. ), or a variant thereof capable of inhibiting CD40-mediated cell activation (Figures 1A-1P) . The amino acids in parentheses are alternatives; one amino acid was found to be coded for in the cloned cDNA and the other amino acid was found to be encoded by the genomic sequence. Thus, it is likely that there are polymorphisms at these sites. This is a 71 amino acid sequence encoded by sequence which is found at the amino-terminal domain of CRAFl nucleic acid as shown in Figures 1A-1P.
In an embodiment of this invention the protein further comprises CRAFl-a (TRAF-3-p55 or CRAFl (p55) ) or a variant thereof adjacent to the carboxy-terminus of the CRAFl-b (TRAF-3-p70 or CRAFl (p55) ) domain. In an embodiment the molecular weight of the CRAFl peptide is about 70 kDa. In another embodiment, an isoform of the CRAFl peptide has a molecular weight of about 5 kDa or about 15 kDa. In an embodiment the CRAFl-b (p70) amino terminal domain comprises at least about 71 amino acids. In another embodiment, it comprises from about 120 to about 150 amino acids. Preferably , it comprises 122 amino acids.
This invention provides a CRAFl peptide having a molecular weight of about 70 kDa. In an embodiment, the CRAFl peptide comprises an amino acid sequence encoded by exons 1-13. In more specific embodiments, the CRAFl peptide comprises an amino acid sequence that is encoded by the exons as shown in the examples in Tables 1 and 2.
As used herein, "variants" encompass the following: Variants can differ from naturally occurring CRAFl peptide (TRAF-3 peptide) in amino acid sequence or in ways that do not involve sequence, or both. Variants in amino acid sequence are produced when one or more amino acids are substituted with a different natural amino acid, an amino acid derivative or non-native amino acid. When a nucleic acid molecule encoding the protein is expressed in a cell, one naturally occurring amino acid will generally be substituted for another. Conservative substitutions typically include the substitution of one amino acid for another with similar characteristics such as substitutions within the following groups: valine, glycine; glycine, alanine; valine, isoleucine; aspartic acid,glutamic acid; asparagine, glutamine; serine, threonine; lysine, arginine; and phenylalanine, tyrosine. The non-polar (hydrophobic) amino acids include alanine, leucine, isoleucine, valine, proline, phenylalanine, tryptophan and methionine . The polar neutral amino acids include glycine, serine, threonine, cysteine, tyrosine, asparagine and glutamine. The positively charged (basic) amino acids include arginine, lysine and histidine. The negatively charged (acidic) amino acids include aspartic acid and glutamic acid.
Other conservative substitutions can be taken from Table A, and yet others are described by Dayhoff in the Atlas of Protein Sequence and Structure (1988) .
Table A: Conservative Amino Acid Replacements
Figure imgf000017_0001
Figure imgf000018_0001
Other variants within the invention are those with modifications which increase peptide stability. Such variants may contain, for example, one or more non- peptide bonds (which replace the peptide bonds) in the peptide sequence. Also included are: variants that include residues other than naturally occurring L-amino acids, such as D-amino acids or non-naturally occurring or synthetic amino acids such as beta or gamma amino acids and cyclic variants. Incorporation of D- instead of L-amino acids into the polypeptide may increase its resistance to proteases. See, e.g., U.S. Patent No. 5,219,990.
The protein of this invention may also be modified by various changes such as insertions, deletions and substitutions, either conservative or nonconservative where such changes might provide for certain advantages in their use. In other embodiments, variants with amino acid substitutions which are less conservative may also result in desired derivatives, e.g., by causing changes in charge, conformation and other biological properties. Such substitutions would include for example, substitution of hydrophilic residue for a hydrophobic residue, substitution of a cysteine or proline for another residue, substitution of a residue having a small side chain for a residue having a bulky side chain or substitution of a residue having a net positive charge for a residue having a net negative charge. When the result of a given substitution cannot be predicted with certainty, the derivatives may be readily assayed according to the methods disclosed herein to determine the presence or absence of the desired characteristics.
Variants within the scope of the invention include proteins and peptides with amino acid sequences having at least eighty percent homology with the CRAFl upstream protein sequence, or CRAFl-b. More preferably the sequence homology is at least ninety percent, or at least ninety-five percent.
Just as it is possible to replace substituents of the scaffold, it is also possible to substitute functional groups which decorate the scaffold with groups characterized by similar features. These substitutions will initially be conservative, i.e., the replacement group will have approximately the same size, shape, hydrophobicity and charge as the original group. Non- sequence modifications may include, for example, in vivo or in vitro chemical derivatization of portions of the protein of this invention, as well as changes in acetylation, methylation, phosphorylation, carboxylation or glycosylation.
In a further embodiment the protein is modified by chemical modifications in which activity is preserved. For example, the proteins may be a idated, sulfated, singly or multiply halogenated, alkylated, carboxylated, or phosphorylated. The protein may also be singly or multiply acylated, such as with an acetyl group, with a farnesyl moiety, or with a fatty acid, which may be saturated, monounsaturated or polyunsaturated. The fatty acid may also be singly or multiply fluorinated. The invention also includes methionine analogs of the protein, for example the methionine sulfone and methionine sulfoxide analogs. The invention also includes salts of the proteins, such as ammonium salts, including alkyl or aryl ammonium salts, sulfate, hydrogen sulfate, phosphate, hydrogen phosphate, dihydrogen phosphate, thiosulfate, carbonate, bicarbonate, benzoate, sulfonate, thiosulfonate, mesylate, ethyl sulfonate and benzensulfonate salts.
This invention provides a method of inhibiting activation by CD40 ligand of cells bearing CD40 on the cell surface, comprising providing the cells with the protein of this invention, the protein being present in an amount effective to inhibit activation of the cells.
The present invention further provides a method of inhibiting activation by CD40 ligand of cells expressing CD40 on the cell surface, comprising providing the cells with the peptide of the invention, the peptide being present in an amount effective to inhibit activation of the cells.
In one embodiment, the cells are provided with the peptide by introducing into the cells a nucleic acid sequence encoding the peptide under conditions such that the cells express an amount of the peptide effective to inhibit activation of the cells. In another emobdiment, the nucleic acid sequence is operably linked to a transcriptional control sequence recognized by the cell. The nucleic acid sequence may be a plasmid. The CD40-bearing cells may be selected from the group consisting of B cells, fibroblasts, endothelial cells, epithelial cells, T cells, basophils, macrophages, Reed-Steinberg cells, dendritic cells, renal cells, and smooth muscle cells. The B cells may be resting B cells, primed B cells, myeloma cells, lyτnphocytic leukemia B cells, or B lymphoma cells. The epithelial cells may be keratinocytes. The fibroblasts may be synovial membrane fibroblasts, dermal fibroblasts, pulmonary fibroblasts, or liver fibroblasts.
The renal cells may be selected from the group consisting of glomerular endothelial cells, mesangial cells, distal tubule cells, proximal tubule cells, parietal epithelial cells, visceral epithelial cells, cells of a Henle limb, and interstitial inflammatory cells.
The parietal epithelial cells may be crescent parietal epithelial cells.
The smooth muscle cells may be smooth muscle cells of the bladder, vascular smooth muscle cells, aortic smooth muscle cells, coronary smooth muscle cells, pulmonary smooth muscle cells, or gastrointestinal smooth muscle cells.
The gastrointestinal smooth muscle cells may be esophageal smooth muscle cells, stomachic smooth muscle cells, smooth muscle cells of the small intestine, or smooth muscle cells of the large intestine.
The invention provides a method of providing a subject with an amount of a CRAF 1 peptide effective to inhibit activation by CD40 ligand of cells bearing CD40 on the cell surface in the subject, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the CRAFl peptide, under conditions such that the cells express in the subject an activation inhibiting effective amount of the peptide.
The introducing of the nucleic acid into cells of the subject may comprise a) treating cells of the subject ex vivo to insert the nucleic acid sequence into the cells; and b) introducing the cells from step a) into the subject.
The subject may be a mammal. The mammalian subject may be a human.
An embodiment of the present invention is a method of treating a condition characterized by an aberrant or unwanted level of CD40-mediated intracellular signaling, in a subject, comprising providing the subject with a therapeutically effective amount of a CRAFl peptide capable of inhibiting CD40-mediated intracellular signaling in cells bearing CD40 on the cell surface.
The peptide may be provided by introducing into CD40- bearing cells of the subject, a nucleic acid sequence encoding the peptide under conditions such that the cells express the peptide according to this method.
The condition may be organ rejection in a subject receiving transplant organs, or an immune response in a subject receiving gene therapy. The transplant organ may be a kidney, heart or liver. The condition may be a CD40-dependent immune response. The CD40-dependent immune response may be an autoimmune response in a subject suffering from an autoimmune disease. The autoimmune disease may comprise rheumatoid arthritis, Myasthenia gravis, systemic lupus erythematosus, Graves' disease, idiopathic thrombocytopenia purpura, he olytic anemia, diabetes mellitus, a drug-induced autoimmune disease, psoriasis, or hyper IgE syndrome.
The drug-induced autoimmune disease may be drug-induced lupus. The immune response may comprise induction of CD23, CD80 upregulation, rescue from CD95-mediated apoptosis, rescue from apoptosis in a subject undergoing chemotherapy against a tumor, or autoimmune manifestations of an infectious disease.
The autoimmune manifestations may be derived from Reiter's syndrome, spondyloarthritis, Lyme disease, HIV infections, syphilis or tuberculosis. The condition may be an allergic response. The allergic response may be hay fever or a penicillin allergy. The condition may be dependent on CD40 ligand-induced activation of fibroblast cells. The condition may be selected from the group consisting of arthritis, scleroderma, and fibrosis. The arthritis may be rheumatoid arthritis, non-rheumatoid inflammatory arthritis, arthritis associated with Lyme disease, or osteoarthritis. The fibrosis may be pulmonary fibrosis, hypersensitivity pulmonary fibrosis, or a pneumoconiosis. The pulmonary fibrosis may be pulmonary fibrosis secondary to adult respiratory distress syndrome, drug-induced pulmonary fibrosis, idiopathic pulmonary fibrosis, or hypersensitivity pneumonitis. The pneumoconiosis may be asbestosis, siliconosis, or Farmer's lung. The fibrosis may be a fibrotic disease of the liver or lung. The fibrotic disease of the lung may be caused by rheumatoid arthritis or scleroderma. The fibrotic disease of the liver may be selected from the group consisting of: Hepatitis-C; Hepatitis-B; cirrhosis; cirrhosis of the liver secondary to a toxic insult; cirrhosis of the liver secondary to drugs; cirrhosis of the liver secondary to a viral infection; and cirrhosis of the liver secondary to an autoimmune disease. The toxic insult may be alcohol consumption. The viral infection may be Hepatitis B, Hepatitis C, or hepatitis non-B non- C. The autoimmune disease may be primary biliary cirrhosis, or Lupoid hepatitis. The condition may be dependent on CD40 ligand-induced activation of endothelial cells. The condition may be selected from the group consisting of atherosclerosis, reperfusion injury, allograft rejection, organ rejection, and chronic inflammatory autoimmune diseases.
The atherosclerosis may be accelerated atherosclerosis associated with organ transplantation.
The chronic inflammatory autoimmune disease may be vasculitis, rheumatoid arthritis, scleroderma, or multiple sclerosis.
The condition may be dependent on CD40 ligand-induced activation of epithelial cells.
In one embodiment of the invention, the epithelial cells are keratinocytes, and the condition is psoriasis.
The condition may be an inflammatory kidney disease. The inflammatory kidney disease may not be initiated by autoantibody deposition in kidney. The kidney disease may be selected from the group consisting of :membranous glomerulonephritis; inimal change disease/acute tubular necrosis,-pauci-immune glomerulonephritis;focal segmental glomerulosclerosis;interstitial nephritis;antitissue antibody-induced glomerular injury;circulating immune- complex disease;a glomerulopathy associated with a multisystem disease; and drug-induced glomerular disease .
The antitissue antibody-induced glomerular injury may be anti-basement membrane antibody disease.
The circulating immune-complex disease may be selected from the group consisting of:infective endocarditis; leprosy; syphilis; hepatitis B; malaria; and a disease associated with an endogenous antigen.
The endogenous antigen may be DNA, thyroglobulin, an autologous immunoglobulin, erythrocyte stroma, a renal tubule antigen, a tumor-specific antigen, or a tumor- associated antigen.
The glomerulopathy may be associated with a multisystem disease is selected from the group consisting of: diabetic nephropathy; systemic lupus erythematosus;Goodpasture's disease; Henoch-Schόnlein purpura; polyarteritis; Wegener's granulomatosis; cryoimmunoglobulinemia; multiple myeloma; Waldenstrδm's macroglobulinemia; and amyloidosis.
The pauci-immune glomerulonephritis may be ANCA+ pauci- immune glomerulonephritis, or Wegener's granulomatosis. The interstitial nephritis may be drug-induced interstitial nephritis. The kidney disease may affect renal tubules. The kidney disease which affects renal tubules may be selected from the group consisting of : a kidney disease associated with a toxin; a neoplasia;hypersensitivity nephropathy; Sjόgren's syndrome; andAIDS.
The condition may be a smooth muscle cell-dependent disease. The smooth muscle cell-dependent disease may be a vascular disease. The vascular disease may be atherosclerosis. The smooth muscle cell-dependent disease may be a gastrointestinal disease. The gastrointestinal disease may be selected from the group consisting of esophageal dys otility, inflammatory bowel disease, and scleroderma. The smooth muscle cell- dependent disease may be a bladder disease.
The condition may be associated with Epstein-Barr virus. The condition may be selected from the group consisting of mononucleosis, B cell tumors, Burkitt's lymphoma, and nasopharyngeal carcinoma. The treatment may not increase susceptibility of the subject to pneumocystis pneumonia, atypical infections, or tumors.
The present invention provides for an isolated nucleic acid molecule encoding a CRAFl peptide. The nucleic acid molecule may be DNA, RNA, cDNA, recombinant DNA, or mRNA.
One embodiment of the invention is a vector comprising the CRAFl nucleic acid molecule or variants or isoforms thereof operably linked to a transcriptional control sequence recognized by a host cell transformed with the vector. The vector may be a plasmid.
The present invention provides a method of differentiating a subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes, comprising: detecting in an extract from a cell derived from the subject, the presence of a nucleic acid encoding the abnormal CD40 receptor-associated factor, thereby differentiating the subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes.
The abnormal CD40 receptor-associated factor polypeptide may be abnormal CD40 receptor-associated factor 1. The subject may be heterozygous for the abnormal CD40 receptor-associated factor. The subject may express CD40 ligand normally. The subject may be a human. The cell may be a B cell. The cell may be derived from a cell culture. The cell may be derived from a bodily fluid.The nucleic acid may encode a truncated CD40 receptor-associated factor polypeptide. The nucleic acid may encode the CD40 receptor-associated factor truncated at the carboxy terminus. The CD40 receptor- associated factor polypeptide may be truncated by at least about 170 amino acid residues. The CD40 receptor- associated factor polypeptide may be truncated by at least about 244 amino acid residues. The nucleic acid may encode the CD40 receptor-associated factor truncated at the amino terminus. The CD40 receptor-associated factor polypeptide may be truncated by at least about 100 amino acid residues. The nucleic acid in the extract may be mRNA, DNA.
The method may further comprise amplifying the nucleic acid prior to detecting, and wherein the detecting is detecting of the amplified nucleic acid.
The detecting may comprise: contacting the nucleic acid to be detected with a probe, wherein, if the nucleic acid to be detected is DNA, the probe is capable of hybridizing to a coding or noncoding strand of a unique sequence encoding a normal CD40 receptor-associate factor; and if the nucleic acid to be detected is RNA, the probe is capable of hybridizing to a unique sequence encoding a normal CD40 receptor-associated factor, under stringent conditions which would permit hybridization with the unique sequence if present; and detecting the absence of a hybrid of the probe and the nucleic acid to be detected, thereby detecting the nucleic acid encoding the abnormal CD40 receptor-associated factor. The probe may comprise at least nine nucleotides, at least twelve nucleotides, or at least fifteen nucleotides. The probe may be labeled. The label may be a radioactive isotope.The label may be iodine-125. The determining may comprise sequencing the nucleic acid.
The present invention provides for a method of providing a subject with an immunosuppressant effective amount of an abnormal CD40 receptor-associated factor, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding an abnormal CD40 receptor-associated factor polypeptide, under conditions such that the cells express in the subject an immunosuppressant effective amount of the abnormal CD40 receptor-associated factor.
One embodiment of the present invention is an antibody or portion thereof capable of specifically binding to a CD40 receptor-associated factor. The CD40 receptor- associated factor may be CD40 receptor-associated factor 1. The antibody may be a monoclonal antibody, a chimeric antibody, or a humanized antibody.
The portion of the antibody may comprise a complementarity determining region or variable region of a light or heavy chain. The portion of the antibody may comprise a complementarity determining region or a variable region, or a Fab.
The present invention provides for a method of differentiating a subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes, comprising: contacting a proteinaceous extract from cells derived from the subject with the antibody or portion thereof under conditions which would permit specific binding of the antibody with normal CD40 receptor-associated factor if present; and detecting the absence of a complex of the antibody with protein in the extract, thereby differentiating a subject with hyper- IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes.
The abnormal CD40 receptor-associated factor polypeptide may be abnormal CD40 receptor-associated factor 1. The subject may express CD40 ligand normally. The subject may be a human. The subject may be a murine animal. The cell may be a B cell. The cell may be derived from a cell culture, or from a bodily fluid.
The abnormal CD40 receptor-associated factor polypeptide may be truncated. The abnormal CD40 receptor-associated factor may be truncated at the carboxy terminus, or by at least about 170 amino acid residues, or by at least about 244 amino acid residues, or at the amino■ terminus, or by at least about 100 amino acid residues.
The antibody or portion thereof may be labeled. The label may be a radioactive isotope such as iodine-125.
The present invention also provides a method for killing a tumor cell which comprises contacting the tumor cell with a CRAFl peptide or variant or isoform thereof so as to activate CD40 signaling and thereby kill the tumor cell. The tumor cell may be a breast tumor cell, a prostate cancer tumor cell, a liver cancer cell, a lung cancer cell, a nasoepithelial cancer cell, an EBV induced tumor cell, a nasopharyngeal tumor cell, an esophogeal cancer cell, a colon cancer cell, a gastric cancer cell, a central nervous system tumor cell, an ovarian cancer cell, or a cervical cancer cell. CD40 signaling may be used as a signal for death in transformed cells (Hess, S. and H. Engelmann. 1996. J". Exp . Med . 183 : 159 ) .
This invention provides for a method of performing anti- tumor therapy with CRAFl: CD40 signaling kills tumor cells by apoptosis, particularly when the tumor cell is a non-B cell. This invention provides for a method for treating a subject suffering from a neoplastic condition which comprises administration of a CRAFl peptide or a variant or an isoform thereof in an effective amount so as to kill a tumor cell and thereby treat the neoplastic condition in the subject. The tumor cell may be stimulated to undergo apoptosis.
The cell may be in a subject suffering from cancer and the CRAFl peptide or variant or isoform thereof is delivered to the tumor cell.
In an embodiment of the method of inhibiting activation by CD40 ligand of cells bearing CD40 on the cell surface, the cells are provided with the protein of this invention by introducing into the cells a nucleic acid sequence encoding the protein under conditions such that the cells express an amount of the protein effective to inhibit activation of the cells. The nucleic acid may be DNA (including cDNA) or RNA. It may be single or double stranded, linear or circular. It may be in the form of a vector such as a plasmid or a viral vector. Preferably the nucleic acid sequence is operably linked to a transcriptional control sequence recognized by the host cell.
In embodiments of the methods described herein, the CD40-bearing cells are selected from the group consisting of B cells, fibroblasts, endothelial cells, epithelial cells, T cells, basophils, macrophages, Reed- Steinberg cells, dendritic cells, myeloma cells, renal cells, and smooth muscle cells. In a more specific embodiment the B cells are resting B cells, primed B cells, myeloma cells, lymphocytic leukemia B cells, or B lymphoma cells. In another specific embodiment the epithelial cells are keratinocytes. In another embodiment the fibroblasts are synovial membrane fibroblasts, dermal fibroblasts, pulmonary fibroblasts, or liver fibroblasts. In another specific embodiment the renal cells are selected from the group consisting of glomerular endothelial cells, mesangial cells, distal tubule cells, proximal tubule cells, parietal epithelial cells (e.g., crescent parietal epithelial cells) , visceral epithelial cells, cells of a Henle limb, and interstitial inflammatory cells. In another embodiment the smooth muscle cells are smooth muscle cells of the bladder, vascular smooth muscle cells, aortic smooth muscle cells, coronary smooth muscle cells, pulmonary smooth muscle cells, or gastrointestinal smooth muscle cells. In a more specific embodiment the gastrointestinal smooth muscle cells are esophageal smooth muscle cells, stomachic smooth muscle cells, smooth muscle cells of the small intestine, or smooth muscle cells of the large intestine.
This invention provides a method of providing a subject with an amount of the protein of this invention effective to inhibit activation by CD40 ligand of cells bearing CD40 on the cell surface in the subject, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein of this invention, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
In an embodiment of this invention the introducing of the nucleic acid into cells of the subject comprises: a) treating cells of the subject ex vivo to insert the nucleic acid sequence into the cells; and b) introducing the cells from step a) into the subject.
The subject which can be treated by the methods described herein is an animal. Preferably the animal is a mammal. Subjects specifically intended for treatment with the method of the invention include humans, as well as nonhuman primates, sheep, horses, cattle, goats, pigs, dogs, cats, rabbits, guinea pigs, hamsters, gerbils, rats and mice, as well as the organs, tumors, and cells derived or originating from these hosts.
This invention provides a method of treating a condition characterized by an aberrant or unwanted level of CD40- mediated intracellular signaling, in a subject, comprising providing the subject with an amount of the peptide of this invention capable of inhibiting CD40- mediated intracellular signaling in cells bearing CD40 on the cell surface. The peptide of the present invention may be a protein.
In an embodiment the protein is provided by introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
In an embodiment the condition is organ rejection in a subject receiving transplant organs. Examples of suitable transplant organs include a kidney, heart or liver, as well as others known to those of skill in the art. In another embodiment the condition is an immune response in a subject receiving gene therapy. One difficulty encountered in gene therapy is an immune response by the patient to the gene therapy vector and the proteins it expresses (Yang, Y. et al . (1996) J. Virol. 70:6370) . Because the protein of this invention inhibits the immune response, gene therapy with the protein of this invention does not trigger an immune response. Its immunosuppressant effect also makes it useful as an adjunct to other forms of gene therapy. For example, at the same time that a vector being administered to provide a gene therapy patient with a desired gene product, the patient is also administered a vector which provides the protein of this invention.
In another embodiment the condition is an allergic response, including but not limited to hay fever or a penicillin allergy, atopic dermatitis and extrinsic asthma.
In an embodiment of this invention the immune response comprises induction of CD23, CD80 upregulation, or rescue from CD95-mediated apoptosis. Because CD40, which is expressed by many tumors, is involved in rescuing cells from apoptosis, inhibitors of CD40- mediated activity are useful as adjunctive agents in chemotherapy.
In an embodiment of this invention the immune response is autoimmune manifestations of an infectious disease. In more specific embodiments the autoimmune manifestations are derived from Reiter's syndrome, spondyloarthritis, Lyme disease, HIV infections, syphilis or tuberculosis.
In an embodiment the condition is dependent on CD40 ligand-induced activation of fibroblast cells, for example arthritis, scleroderma, and fibrosis. In more specific embodiments the arthritis is rheumatoid arthritis, non-rheumatoid inflammatory arthritis, arthritis associated with Lyme disease, or osteoarthritis. In another specific embodiment the fibrosis is pulmonary fibrosis, hypersensitivity pulmonary fibrosis, or a pneumoconiosis. Examples of pulmonary fibrosis include pulmonary fibrosis secondary to adult respiratory distress syndrome, drug-induced pulmonary fibrosis, idiopathic pulmonary fibrosis, or hypersensitivity pneumonitis. Examples of pneumoconiosis include asbestosis, siliconosis, or Farmer's lung. In another specific embodiment the fibrosis is a fibrotic disease of the liver or lung, including fibrotic disease of the lung caused by rheumatoid arthritis or scleroderma, and fibrotic diseases of the liver selected from the group consisting of: Hepatitis-C; Hepatitis-B; cirrhosis; cirrhosis of the liver secondary to a toxic insult; cirrhosis of the liver secondary to drugs; cirrhosis of the liver secondary to a viral infection; and cirrhosis of the liver secondary to an autoimmune disease. In a specific embodiment the toxic insult is alcohol consumption. In another specific embodiment the viral infection is Hepatitis B, Hepatitis C, or hepatitis non-B non-C. In another specific embodiment the autoimmune disease is primary biliary cirrhosis, or Lupoid hepatitis.
In an embodiment of this method the condition is dependent on CD40 ligand-induced activation of endothelial cells. In specific embodiments the condition dependent on CD40 ligand-induced activation of endothelial cells is selected from the group consisting of atherosclerosis, reperfusion injury, allograft rejection, organ rejection, and chronic inflammatory autoimmune diseases. In a more specific embodiment the atherosclerosis is accelerated atherosclerosis associated with organ transplantation. In another specific embodiment the chronic inflammatory autoimmune disease is vasculitis, rheumatoid arthritis, scleroderma, or multiple sclerosis.
In an embodiment the condition is dependent on CD40 ligand-induced activation of epithelial cells. In a specific embodiment the epithelial cells are keratinocytes, and the condition is psoriasis. In another specific embodiment the condition is an inflammatory kidney disease, including inflammatory kidney disease not initiated by autoantibody deposition in kidney and kidney disease which is initiated by autoantibody deposition. In specific embodiments the kidney disease is selected from the group consisting of : membranous glomerulonephritis; minimal change disease/acute tubular necrosis; pauci-immune glomerulonephritis; focal segmental glomerulosclerosis; interstitial nephritis; antitissue antibody-induced glomerular injury; circulating immune-complex disease; a glomerulopathy associated with a multisystem disease; and drug-induced glomerular disease. In an embodiment the antitissue antibody-induced glomerular injury is anti-basement membrane antibody disease. In another embodiment the circulating immune-complex disease is selected from the group consisting of: infective endocarditis; leprosy; syphilis; hepatitis B; malaria; and a disease associated with an endogenous antigen. In a more specific embodiment the endogenous antigen is DNA, thyroglobulin, an autologous immunoglobulin, erythrocyte stroma, a renal tubule antigen, a tumor- specific antigen, or a tumor-associated antigen. In another embodiment the glomerulopathy associated with a multisystem disease is selected from the group consisting of: diabetic nephropathy; systemic lupus erythematosus; Goodpasture's disease; Henoch-Schδnlein purpura; polyarteritis; Wegener's granulomatosis; cryoimmunoglobulinemia; multiple myeloma; Waldenstrόm's macroglobulinemia; and amyloidosis . In an embodiment the pauci-immune glomerulonephritis is ANCA+ pauci- immune glomerulonephritis, or Wegener's granulomatosis. In an embodiment the interstitial nephritis is drug- induced interstitial nephritis. In another embodiment the kidney disease affects renal tubules, including but not limited to: a kidney disease associated with a toxin; a neoplasia; hypersensitivity nephropathy; Sjogren's syndrome; and AIDS.
In an embodiment the condition is a smooth muscle cell- dependent disease. Examples include vascular diseases such as atherosclerosis; gastrointestinal diseases such as esophageal dys otility, inflammatory bowel disease, and scleroderma; and bladder diseases.
In an embodiment of this method, the condition is associated with Epstein-Barr virus. Examples of Epstein-Barr virus-associated conditions include mononucleosis, B cell tumors (particularly in immunosuppressed individuals such as chemotherapy patients and those with acquired immune deficiency syndrome (AIDS) ) , Burkitt's lymphoma, and nasopharyngeal carcinoma. Epstein-Barr virus (EBV) transforms cells using latent infection membrane protein 1 (LMP1) . LMP1 binds to CRAFl (also known as LAP1) (33) .
Inhibition of the immune response using an antibody against CD40L may potentially making the patient susceptible to pneumocystis pneumonia. Hyper IgM patients who have defective B cell activation signaling, do not get pneumocystis pneumonia, other atypical infections, and tumors. The data presented herein indicate that people with the 70 kDa isoform of CRAFl are a subset of these patients. Accordingly, in an embodiment of the above-described method of treating a subject, the treatment does not increase susceptibility of the subject to atypical infections (e.g., pneumocystis pneumonia) or tumors.
This invention provides a nucleic acid molecule encoding the protein of this invention. The nucleic acid may be DNA (including cDNA) or RNA. It may be single or double stranded, linear or circular. It may be in the form of a vector, such as a plasmid or viral vector, which comprises the nucleic acid molecule operably linked to a transcriptional control sequence recognized by a host cell transformed with the vector. In one embodiment the DNA molecule comprises the coding strand of the CRAFl IHb clone (Figures 1A-1P) . In another embodiment the DNA molecule is complementary to the coding strand of the CRAFl IHb clone. In a specific embodiment the plasmid is pBluescriptSKII+/IIIb.
This invention provides an isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers; wherein when the protein comprises zinc fingers 1, 2 and 5, the protein further comprises one or both of zinc fingers 3 and 4.
The numbering of CRAFl zinc finger domains is based on the schematic shown in Figure 4. The zinc finger domains are numbered consecutively from 1 to 5, proceeding from the amino terminus to the carboxy terminus. The zinc fingers, if any, in the protein of this invention, may be present in the order in which they appear in wild-type CRAF-1 (e.g., N-l, 3, 4, 5-C) or in a different order (e.g. N-l, 4, 5-C) . A zinc finger domain can be eliminated by deleting the corresponding exon or part of the exon, or by other mutagenesis techniques, for example a point mutation which changes a zinc finger cysteine or histidine to another amino acid which disrupts the zinc finger domain structure.
CRAFl proteins or variants thereof comprising from zero to four zinc finger domains of this invention may be capable of inhibiting CD40-mediated cell activation in vitro and in vivo. In an embodiment of this invention the protein comprises zero, one, two or four zinc fingers. In another embodiment, the protein comprises CRAFl or variant thereof deleted by zinc finger domains 2, 3 and 4, or by exons 8, 9, and 10 in the zinc finger domain encoding region. In another embodiment the protein comprises CRAFl or variant thereof deleted by amino acids 191 to 242. In specific embodiments the protein is CRAFla deleted by amino acids 191 to 242 or CRAFlb deleted by amino acids 313 to 364. The deletions of these amino acids result in the formation of new zinc finger domains comprised of different groups of amino acids.
In an embodiment of this invention, the variant comprises a conservative amino acid substitution. Variants can differ from naturally occurring CRAFl and isoforms thereof comprising from one to four zinc fingers, in amino acid sequence or in ways that do not involve sequence, or both.
This invention provides a method of inhibiting activation by CD40 ligand of cells bearing CD40 on the cell surface, comprising providing the cells with an isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers, the protein being present in an amount effective to inhibit activation of the cells.
In an embodiment of the method of inhibiting activation by CD40 ligand of cells bearing CD40 on the cell surface, the cells are provided with isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers by introducing into the cells a nucleic acid sequence encoding the protein under conditions such that the cells express an amount of the protein effective to inhibit activation of the cells. The nucleic acid may be DNA (including cDNA) or RNA. It may be single or double stranded, linear or circular. It may be in the form of a vector such as a plasmid or a viral vector. Preferably the nucleic acid sequence is operably linked to a transcriptional control sequence recognized by the host cell.
This invention provides a method of providing a subject with an amount of isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers effective to inhibit activation by CD40 ligand of cells bearing CD40 on the cell surface in the subject, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
In one embodiment, the protein comprises CRAFl or variant thereof, deleted by amino acids 218 to 242. In specific embodiments the protein is CRAFla deleted by amino acids 218 to 242 or CRAFlb deleted by amino acids 340 to 364. In another embodiment the protein comprises CRAFl or variant thereof, deleted by amino acids 191 to 242. In specific embodiments the protein is CRAFla deleted by amino acids 191 to 242 or CRAF lb deleted by amino acids 313 to 364.
In an embodiment of this invention the introducing of the nucleic acid into cells of the subject comprises: a) treating cells of the subject ex vivo to insert the nucleic acid sequence into the cells; and b) introducing the cells from step a) into the subject.
This invention provides a method of treating a condition characterized by an aberrant or unwanted level of CD40- mediated intracellular signaling, in a subject, comprising providing the subject with an amount of an isolated CRAFl protein or variant thereof comprising from zero to four zinc fingers capable of inhibiting CD40-mediated intracellular signaling in cells bearing CD40 on the cell surface.
In an embodiment the protein is provided by introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
In another embodiment the condition is a CD40-dependent immune response. In a specific embodiment the CD40- dependent immune response is an autoimmune response in a subject suffering from an autoimmune disease, including but not limited to rheumatoid arthritis, Myasthenia gravis, systemic lupus erythematosus, Graves' disease, idiopathic thrombocytopenia purpura, hemolytic anemia, diabetes mellitus, a drug-induced autoimmune disease such as drug-induced lupus, psoriasis, hyper IgE syndrome, or abdominal aortic aneurism (AAA) .
This invention provides a nucleic acid molecule encoding the peptide of this invention. The nucleic acid may be DNA (including cDNA) or RNA or mRNA. It may be single or double stranded, linear or circular. It may be in the form of a vector, such as a plasmid or viral vector, which comprises the nucleic acid molecule operably linked to a transcriptional control sequence recognized by a host cell transformed with the vector. In one embodiment the nucleic acid molecule encodes a CRAFl peptide that does not contain exon 9 (Figures 1A-1P) . The nucleic acid can be a coding strand or complementary to the coding strand or a reverse complement to the coding strand. In specific embodiments the CRAFl nucleic acid molecule may be any of the specific sequences shown in Figures 1A-1P and in Tables 1 and 2. This invention provides a method of providing a subject with an amount of a CRAFl protein or variant thereof comprising from zero to four zinc fingers, effective to inhibit activation by CD40 ligand of cells bearing CD40 on the cell surface in the subject, comprising: introducing into CD40-bearing cells of the subject an agent capable of enhancing RNA splicing, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
In one embodiment the agent is a splicing apparatus element.
In embodiments of this method, the element is a protein; an RNA, for example a a small nuclear RNA (snRNA) ; or a small nuclear ribonucleoprotein (snRNP) . In another embodiment the agent is a vector encoding a splicing apparatus element.
The agent can enhance nonspecific RNA splicing, or it can specifically affect CRAFl RNA splicing. In embodiments of this invention the agent enhances downstream splicing, or upstream splicing.
In an embodiment of this invention the agent enhances formation of a spliceosome, wherein the spliceosome comprises pre-mRNA encoding the CRAFl protein or variant thereof comprising from zero to four zinc fingers.
This invention provides a method of differentiating a subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes, comprising: detecting in an extract from a cell derived from the subject, the presence of a nucleic acid encoding the abnormal CD40 receptor-associated factor, thereby differentiating the subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes.
In a preferred embodiment the abnormal CD40 receptor- associated factor polypeptide is abnormal CD40 receptor- associated factor 1.
As described in the Experimental Methods section below, the expression of mutant or truncated forms of CRAF! Can serve as a dominant negative. Accordingly, in a specific embodiment the subject is heterozygous for the abnormal CD40 receptor-associated factor.
In an embodiment of this invention the subject with hyper -IgM syndrome expresses CD40 ligand normally.
In a preferred embodiment the cell from which the extract is derived is a B cell. The cell may be derived from a cell culture or from a bodily fluid, including but not limited to blood.
The gene encoding abnormal CRAF may contain point mutations, frame shift mutations, a premature stop codon. Alternatively, it may be missing a segment of the gene at the 5' or 3' end of the coding region. In an embodiment of this invention the nucleic acid encodes a truncated CD40 receptor-associated factor polypeptide. In a specific embodiment the the nucleic acid encodes the CD40 receptor-associated factor truncated at the carboxy terminus. In more specific embodiments the carboxy-terminal truncated CRAF is truncated by at least about 170 amino acid residues, or by at least about 244 amino acid residues. In another specific embodiment the nucleic acid encodes the CD40 receptor-associated factor truncated at the amino terminus. In a more specific embodiment the amino-terminal truncated CRAF is truncated by at least about 171 amino acid residues or 258 amino acids.
The nucleic acid present in the extract can be RNA or DNA. It can be single stranded or double stranded. In an embodiment the nucleic acid in the extract is mRNA. In another embodiment the nucleic acid in the extract is DNA, including single stranded and double stranded DNA.
In an embodiment the nucleic acid is amplified prior to detecting, and the detecting is detecting of the amplified nucleic acid. When the nucleic acid is mRNA a cDNA copy is preferably made by reverse transcription. Reverse transcriptase is commercially available, for example from New England Biolabs (Beverly, MA) . PCR, a well known laboratory technique (See for example
Sambrook, et al. , Molecular Cloning: A Laboratory Manual
(Cold Spring Harbor, 1989) ch. 14) , is the preferred for amplifying the nucleic acid.
In one embodiment of this invention the detecting comprises: contacting the nucleic acid to be detected with a probe, wherein, if the nucleic acid to be detected is DNA, the probe is capable of hybridizing to a coding or noncoding strand of a unique sequence encoding a normal CD40 receptor-associate factor; and if the nucleic acid to be detected is RNA, the probe is capable of hybridizing to a unique sequence encoding a normal CD40 receptor-associated factor, under stringent conditions which would permit hybridization with the unique sequence if present; and detecting the absence of a hybrid of the probe and the nucleic acid to be detected, thereby detecting the nucleic acid encoding the abnormal CD40 receptor-associated factor. The length of the probe should be chosen to provide a high probability that it will recognize a unique sequence. This will depend in part on the length of the genome of the subject and can be easily calculated by one of skill in the art to which this invention pertains. In specific embodiments the probe comprises at least nine nucleotides, at least twelve nucleotides, or at least fifteen nucleotides. In an embodiment the probe is labeled. In a specific embodiment the label is a radioactive isotope. A number of suitable radioactive isotopes are known to those of skill in the art, including but not limited to iodine-125.
This invention also provides a method of providing a subject with an immunosuppressant effective amount of an abnormal CD40 receptor-associated factor, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding an abnormal CD40 receptor-associated factor polypeptide, under conditions such that the cells express in the subject an immunosuppressant effective amount of the abnormal CD40 receptor-associated factor.
Gene therapy for providing a subject with a protein encoded by a gene are described in U.S. Patent No. 5,399,346, issued March 21, 1995 (Anderson, et al. ) . A nucleic acid sequence encoding the protein of interest can be inserted into cells of the subject in vivo. Alternatively the nucleic acid can be inserted into cells ex vivo and the transfected cells can then be introduced into the subject. Accordingly, in an embodiment the introducing of the nucleic acid into cells of the subject comprises: a) treating cells of the subject ex vivo to insert the nucleic acid sequence into the cells; and b) introducing the cells from step a) into the subject.
In an embodiment of this invention the abnormal CD40 receptor-associated factor polypeptide is abnormal CD40 receptor-associated factor 1. In an embodiment of this invention the nucleic acid sequence encodes a truncated CD40 receptor-associated factor polypeptide. In a specific embodiment the nucleic acid sequence encodes CD40 receptor-associated factor polypeptide truncated at the amino terminus. In a more specific embodiment the amino-terminal truncated CD40 receptor-associated factor polypeptide is truncated by at least about 171 amino acid residues. In another specific embodiment the amino-terminal truncated CD40 receptor-associated factor polypeptide is truncated by at least about 323 amino acid residues. In another specific embodiment the nucleic acid sequence encodes CD40 receptor-associated factor polypeptide truncated at the carboxy terminus. In a more specific embodiment the carboxy-terminal truncated CD40 receptor-associated factor polypeptide is truncated by at least about 258 amino acid residues.
This invention provides a method of inhibiting a CD40- dependent immune response in a subject, comprising providing the subject with an immunosuppressant effective amount of an abnormal CD40 receptor-associated factor by a method which comprises introducing into
CD40-bearing cells of the subject, a nucleic acid sequence encoding an abnormal CD40 receptor-associated factor polypeptide, under conditions such that the cells express in the subject an immunosuppressant effective amount of the abnormal CD40 receptor-associated factor as described above.
In specific embodiments the immune response which is inhibited comprises induction of CD23, CD80 upregulation, or rescue from CD95-mediated apoptosis.
This invention also provides an antibody or portion thereof capable of specifically binding to a CD40 receptor-associated factor. Techniques for producing antibodies are well known in the art and are described in standard laboratory manuals, such as Harlow and Lane, Antibodies: A Laboratory Manual (Cold Spring Harbor 1988) pp. 53-138. The CRAF protein, whether purified or recombinant, is preferably coupled to a carrier protein. Examples of useful carrier proteins include keyhole limpet hemacyanin, ovalbumin, bovine serum albumin, mouse serum albumin, and rabbit serum albumin. The CRAF, alone or coupled to a carrier protein, is injected into an animal, for example a mouse or rabbit in order to immunize it. Antibodies against the CRAF are then isolated from the immunized animal
In a specific embodiment of this invention the CD40 receptor-associated factor is CD40 receptor-associated factor 1.
The antibody may be either a polyclonal or monoclonal antibody. The production of monoclonal antibodies using hybridoma technology are well known to those of skill in the art and are described in standard laboratory manuals, such as Harlow and Lane, Antibodies: A Laboratory Manual (Cold Spring Harbor 1988) pp. 139-282.
In specific embodiments the monoclonal antibody is a chimeric antibody or a humanized antibody. The meaning of "chimeric" and "humanized" antibody and methods of producing them are well known to those of skill in the art and are described, for example, in PCT International Publication No. WO 90/07861, published July 26, 1990 (Queen, et al.) ; and Queen, et al . Proc. Nat'l Acad. Sci. -USA (1989) 86: 10029) .
In another embodiment the portion of the antibody comprises a complementarity determining region or variable region of a light or heavy chain. In yet another embodiment the portion of the antibody comprises a complementarity determining region or a variable region. In an embodiment the portion of the antibody comprises a Fab.
This invention provides a method of differentiating a subject with hyper-IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes, comprising: contacting a proteinaceous extract from cells derived from the subject with the antibody or portion thereof as described above under conditions which would permit specific binding of the antibody with normal CD40 receptor-associated factor if present; and detecting the absence of a complex of the antibody with protein in the extract, thereby differentiating a subject with hyper- IgM syndrome due to an abnormal CD40 receptor-associated factor polypeptide from those with hyper-IgM syndrome due to other causes.
In an embodiment the abnormal CD40 receptor-associated factor polypeptide is abnormal CD40 receptor-associated factor 1.
In an embodiment the subject expresses CD40 ligand normally.
In an embodiment of this invention the abnormal CD40 receptor-associated factor polypeptide is truncated at the carboxy terminus or the amino-terminus . In a specific embodiment the carboxy-terminal truncated abnormal CD40 receptor-associated factor polypeptide is truncated by at least about 171 amino acid residues. In another specific embodiment the abnormal CD40 receptor- associated factor polypeptide is truncated by at least about 244 amino acid residues. In another specific embodiment the amino-terminal truncated abnormal CD40 receptor-associated factor polypeptide is truncated by at least about 258 amino acid residues.
In an embodiment of this invention the antibody or portion thereof is labeled. In a specific embodiment the antibody or portion thereof is labeled with a radioactive isotope. Suitable radioisotopes are known to those of skill in the art and include, but are not limited to iodine-125.
This invention will be better understood from the Experimental Details which follow. However, one skilled in the art will readily appreciate that the specific methods and results discussed are merely illustrative of the invention as described more fully in the claims which follow thereafter.
Experimental Details
The following two tables (Tables 1 and 2) provide some details about several embodiments of the present invention such as exon structure, splice donor and splice acceptor sites, base pair number, etc.
Table 1. Structure of TRAF-3 mRNAs and Putative Peptide Isoforms
Exons
Figure imgf000049_0001
►Prev ous y reporte as CRAF-1, AP-l ♦♦Previously reported as CD40-bp ♦♦♦Previously reported as CAP-1 + 2-1 type transcripts also encode TRAF-3(p5) ++Ib type transcripts also encode TRAF-3(pl5) Note: exon 8 encodes aa 191-217 of TRAF-3 (p55) exon 9 enocodes aa 218-242 of TRAF-3 (p55) exon 10 encodes aa 242-273 of TRAF-3 (ρ55) Table 2. Genomic Structure of TRAF-3
Figure imgf000050_0001
Note: where ambiguous, boundary assignments optimize gt/ag consensus.
* intron class : 0 : }xn falls between codons , 1 : }xn falls after 1st nt of codon, 2 : ;jxn falls after 2nd nt of codon .
359-540 Zn r ng, 550-1015 Zn fingers, 1080-1250 Helical Wheel, 1290- stop TRAF domain ( 1470-stop TRAF-C domain)
Example 1 : Complementary DNA Encoding Long CRAFl Isoform Several cDNA species encoding human CRAFl nucleic acid from a Raj i B cell library (several of which are described in Tables 1 and 2 ) have been isolated that reveal unexpected complexity in the 5' -region of these cDNAs . Although divergent in some cases , comparison of the sequences of these clones suggests at least 8 unique segments, several of which are shared between the cDNA clones and are therefore highly suggestive of alternative splicing events. Given the identity of several distinct cDNA sequence elements between these clones, alternative splicing may account for at least some of these data. However, the formal possibility exists that CRAFl peptide is encoded by several distinct genes. From the sequences of these cDNAs, it can be inferred that at least putative eight exons exist. These exons have been assigned number codes (i.e., 1- 13) . The organization and arrangement of these exons is shown in Figures 2A and 2B and Figure 3. Figures 1A-1P show the sequences of exons 1-13. The exon boundaries shown in Figures 1A-1P are derived from the comparison of cDNA sequences. They may be adjusted by a few nucleotides based on genomic sequencing.
Many of the cDNA species are expected to yield proteins with the published 568 aa sequence of CRAFl (p55) (75) since an upstream in frame stop codon is present. However, at least one of these species, represented by cDNA clone IHb (ATCC Accession No. 97489) contains an open reading frame that is not interrupted by a stop codon (Figures 1A-1P) and Genbank Accession number U21092) . The predicted amino acid sequence of the IHb clone preceding the published
MESSKKD- start site is : ( - 71 - GARRGRRVREPGLQPSRDFPAGGSRGGRRLFPAPRHGAARGA(E/K) (R/C) CG PRR(Q/R)TRPAPLSRPSGDGP(Q/R)ELLFPK-1) (Seq I.D. No. ) . The structure of this domain is highly charged as indicated by the presence of 18/71 arginine residues. It also appears to be an extended strand as evidenced by the presence of 13/71 glycines and 11/71 prolines. In fact, the arginine, glycine and proline content of this putative sub-domain comprises 42/71 of the residues. It does not have homology to any other sequence in GenBank, and does not have an identifiable motif that suggests its function. Two arginine and proline-rich domain motifs have been described (SH.-binding domain, and WW domain) . This sequence does not appear to be either of these two, based on amino acids -71 to -1.
However, the new amino-terminal domain of TRAF-3 p70 described by the first 71 aa has some features of an Src homology 3 (SH3) -binding domain protein (Alexandropoulos, K. , et al. (1995)PNAS, 92:3110; Cohen, G. B., et al. 1995. Cell 80:237) . The sequence aa 103- RPAPLSRP-110 (present in both p70-i and pl5) is similar to the RPLPXXP motif that accounts for SH3- binding in other proteins. In addition, by the criteria of the PXXP motif, (Saksela, K., et al . 1995. EMBO Journal 14:484), the novel amino terminal domain of p70 (that is shared by p5 and pl5) contains the sequences: 16-PQRP-19 and 44-PCPP-47.
As used herein, patient H is the same as patient A; patient L is the same as patient B; patient S is the same as patient D; mother of patient C is the same as CM; mother of patient D is the same as DM and the same as RS.
To determine if the IHb-type cDNA (CRAFl peptide, TRAF- 3-p55) is represented by mRNA in normal and hyper IgM B cells that have been EBV-transformed, RT-PCR was performed on mRNA from three EBV transformed B cell lines; one from a normal subject and two from the HIM patients A and B, by priming the RT reaction with 3'- reverse primer and amplifying with the primer pair oCRf (127-144) /oCRr(675-658) (predicted product (127- 675) for a 548 bp product) . The oCRf (127-144) anneals to a region in exon 2 and oCRr(675-658) anneals to the conserved exon 4-13 region shared by all cDNAs. (These nucleotide numbers refer to nucleotides in the sequence shown in Figures 1A-1P. Primers in which the first number is higher than the second are reverse nucleotide primers.) Two bands were excised from the gel, cloned in the TA system (pCRII, Invitrogen*) and sequenced. The amplified 548 bp band corresponds exactly to sequence of the [exons 2,4-13] product (analogous to IHb) . These results strongly suggest that species of the [exons 2, 4-13] product are found in B cells. In addition, these data suggest that the protein isoform of which the [exons 2, 4-13] transcript is a partial cDNA clone of a species that exists in normal cells. Thus, this protein isoform is termed the CRAFl-b isoform (TRAF-3-p-70) , in contrast to the protein isoform encoded by transcript which initiates translation at methionine 1 (nucleotides 675-678 of Figures 1A-1P) , which is termed CRAFl-a (TRAF- 3-p-55) .
Characterization of CRAFl Peptides
Immunoprecipitation of metabolically labelled Ramos cells, Ramos/pCEP/CRAFl and EBV-transformed B cell lines was performed using rabbit antisera against the peptide representing CRAFl peptide amino-terminus. Several bands are specifically immunoprecipitated by the anti- CRAF1 antisera, including major bands that migrate at 70 kDa and 60 kDa. The intensity of the 60 kDa band is strongly increased in lysates from Ramos/pCEP/CRAFl cells, which
Figure imgf000053_0001
that this band represents the peptide product of the CRAFl-a transcript and which is consistent with the predicted molecular weight of a 568 aa peptide. The expression of both the 60 kDa band and the 70 kDa band is greatly increased in the EBV transformed cells relative to the intensity of these bands in Ramos controls suggesting that EBV transformation increases the expression of CRAFl peptides and which is consistent with the observation by Kieff and coworkers that EBV upregulates CRAFl mRNA in BJAB cells (98) . CRAFl-encoded peptides in two unrelated HIM patients
Defective CD40-L molecules underlie a genetic immune deficiency syndrome, the X-linked hyper-IgM syndrome
(HIGMX-1) , in which B cell differentiation is blocked at the IgM expressing stage and in which germinal centers are absent (12-21) . Furthermore, the essential roles of
CD40-L in the IgG'IgA'IgE" phenotype of HIM syndrome has been confirmed by targeted disruption of CD40-L in mice
(23,24) . However, HIM syndrome does not always involve defects in CD40-L (74,22) . In mice, targeted disruption of CD40 results in a phenotype similar to HIM (25,26) .
Patients A and B have normal CD40-L expression by the mAb 5c8 and normal expression of CD40 by the mAb G28-5. Both patients A and B are relatively healthy, since they are 49 and 27 years old, respectively, and have not developed neoplastic disease, nor has either had pneumocystis, opportunistic infections or neutropenia, which are features of HIGMX-1 (74) .
In order to test whether these hyper IgM patients have a defect in their CRAFl nucleic acid or their CRAFl peptide, the peptide products of the CRAFl gene were analyzed using a rabbit antiserum generated to the NH2- terminus of the CRAFl peptide. Immunoprecipitation followed by Western blotting with the CRAFl-specific antisera from EBV-transformed B cell lines from a normal individual and from the hyper-IgM patients A, B and C was performed (Figure 5) . The anti-CRAFl antisera specifically identified peptide species that migrate at 70 kDa and 60 kDa. The expression of the p60 CRAFl is comparable in all the cell lines examined except the EBV-transformed B cells from patient B, in which only trace amounts of the p60 CRAFl was detected. This result shows that p60 CRAFl is normally expressed in B lymphocytes. A high molecular weight CRAFl peptide species, p70 CRAFl (TRAF-3-p70) , was identified in EBV- transformed B cells (lanes 9-12) , but not in non-EBV- transformed cell lines. However the expression level of p70 CRAFl varies. In EBV-transformed B cells established from normal B lymphocytes, p70 CRAF is only expressed at low levels (lane 9) . However, in EBV- transformed B cells from patient A, the expression of p60 CRAF and p70 CRAFl is comparable (lane 10) . Moreover, in EBV-transformed B cells from patient B, the expression of p70 CRAFl is not only dominant but also dramatically up-regulated. Furthermore, in patient B only trace amounts of the p60 CRAFl was detected (lane 11) . In contrast to hyper IgM patients A and B (which are known to have normal CD40L) in EBV-transformed cells established from patient C, the p70 CRAFl expression is below the level of detection (lane 12) .
The lysates from all the cells examined (except for those from patient C) contain both protein species, suggesting that if these patients have a mutated CRAFl nucleic acid allele, a normal CRAFl nucleic acid allele may also be present. The presence of increased amounts of p70 in these two hyper IgM patients (patients A and B) suggests that the p70 protein is an inhibitory protein relative to CD40 signaling.
Sequencing Larger CRAFl Isoforms and cDNA This invention provides various means for determining the amino acid sequence of CRAFl peptide isoforms which are longer than CRAFl-b (CRAFl p70 or TRAF-3-p70) , i.e. which have additional amino acid residues N-terminal to residue -72, as well as nucleic acid sequences coding for such longer isoforms. The IHb clone (p55 CRAFl nucleic acid) is a partial cDNA clone and that the upstream sequence of full length IIlb-type transcripts do encode a larger peptide. This was confirmed by the identification of an upstream methionine with an appropriate adjacent Kozack sequence. In one technique, the 70 kDa CRAFl peptide isoform (CRAFl (p70) or TRAF-3-p70) is isolated using an anti- CRAF1 antibody, and its amino terminus sequence determined. Based on the amino-terminal protein sequence, degenerate oligonucleotides are designed which anneal to the corresponding mRNA, cDNA or genomic DNA. Using standard techniques, these degenerate oligonucleotides are used to clone cDNA that encodes the 70 kDa CRAFl peptide isoform.
In another technique, using the cDNA sequence of CRAFl nucleic acid IHb, cDNA libraries or genomic libraries are screened for DNA sequences upstream of that shown. The encoded amino acid sequence is deduced based on the DNA sequence of the upstream clone.
In another technique, the upstream sequence can be determined using RACE (Rapid Amplification of cDNA Ends) . RACE kits are commercially available from BOEHRINGER MANNHEIM* and others. First strand cDNA is synthesized from total or poly(A) + RNA using a gene specific primer, reverse transcriptase, and a mixture of deoxynucleotides. After purification from unincorporated nucleotides and primers, terminal transferase is used to add a homolypolymeric A-tail to the 3' end of the cDNA. Tailed cDNA is then amplified by PCR using a gene specific primer and an oligo dT- primer. The cDNA obtained thereby is further amplified. It is then sequenced, and the corresponding protein sequence deduced.
In another technique, the upstream sequence is determined using anchored PCR. For example, anchored PCR is used on the template of Raji cDNA library DNA to identify the sequence further 5'-to what is included in the IHb clone. As a primer in exon 2 in CRAFl the reverse primer, oCRr (144-126) is used. As anchoring primers in λgtll in separate reactions, any (since the library is not cloned directionally) of the following are used: oλgf (1033-1056) (5'-ggT ggC gAC gAC TCC Tgg
AgC Ccg) (Seq I.D. No. ), oλgr(1119-1097) (5'-TTg ACA CCA gAC CAA CTg gTA ATg) (Seq I.D. No. ) , oλgr(1096-
1082) (5'-ggT AgC gAC Cgg CgC) (Seq I.D. No. ) or oλgf (998-1015) (5' -CAT ggC TgA ATA TCg Acg) (Seq I.D. No. ) . PCR products are generated using this technique.
To determine their relationship to the IIlb-like transcripts, these PCR amplified cDNA fragments are cloned in the TA cloning system (Invitrogen) and sequenced. The sequences are compared to IHb.
Gene Therapy The invention features expression vectors for in vivo transfection and expression in particular cell types of CD40 receptor-associated factor truncated at the amino terminus so as to antagonize the function of wild type CD40 receptor-associated factor in an environment in which the wild-type protein is expressed (i.e., introduce abnormal CD40 receptor-associated factor that acts as a dominant negative protein to inhibit CD40 signaling) .
Expression constructs of CD40 receptor-associated factor polypeptides may be administered in any biologically effective carrier that is capable of effectively delivering a polynucleotide sequence encoding the CD40 receptor-associated factor to cells in vivo. Approaches include insertion of the subject gene in viral vectors including recombinant retroviruses, baculovirus, adenovirus, adeno-associated virus and herpes simplex virus-1, or recombinant bacterial or eukaryotic plasmids. Viral vectors transfect cells directly, plasmid DNA can be delivered with the help of, for , example, cationic liposomes or derivatized (e.g., antibody conjugated) polylysine conjugates, gramacidin S, artificial viral envelopes or other such intracellular carriers, as well as direct injection of the gene construct or CaP04 precipitation carried out in vivo.
Any of the methods known in the art for the insertion of polynucleotide sequences into a vector may be used. See, for example, Sambrook et al. , Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY (1989) and Ausubel et al., Current Protocols in Molecular Biology, J. Wiley & Sons, NY (1992) , both of which are incorporated herein by reference. Conventional vectors consist of appropriate transcriptional/translational control signals operatively linked to the polynucleotide sequence for a particular anti-fibrotic polynucleotide sequence. Promoters/enhancers may also be used to control expression of anti-fibrotic polypeptide. Promoter activation may be tissue specific or inducible by a metabolic product or administered substance. Such promoters/enhancers include, but are not limited to, the native E2F promoter, the cytomegalovirus immediate-early promoter/enhancer (Karasuyama et al. , J. Exp . Med. , 169: 13 (1989) ) ; the human beta-actin promoter (Gunning et al., Proc . Na tl . Acad . Sci . USA, 84: 4831 (1987) ; the glucocorticoid-inducible promoter present in the mouse mammary tumor virus long terminal repeat (MMTV LTR)
(Klessig et al. , Mol . Cell . Biol . , 4: 1354 (1984)) ; the long terminal repeat sequences of Moloney murine leukemia virus (MuLV LTR) (Weiss et al. , RNA Tumor
Viruses, Cold Spring Harbor Laboratory, Cold Spring
Harbor, NY (1985) ) ; the SV40 early region promoter
(Bernoist and Chambon, Nature, 290:304 (1981)) ; the promoter of the Rous sarcoma virus (RSV) (Yamamoto et al . , Cell , 22:787 (1980)) ; the herpes simplex virus (HSV) thymidine kinase promoter (Wagner et al. , Proc . Na tl . Acad . Sci . USA, 78: 1441 (1981)) ; the adenovirus promoter (Yamada et al. , Proc . Natl . Acad. Sci . USA, 82: 3567 (1985) ) .
Expression vectors compatible with mammalian host cells for use in gene therapy of tumor cells include, for example, plasmids; avian, murine and human retroviral vectors; adenovirus vectors; herpes viral vectors; and non-replicative pox viruses. In particular, replication-defective recombinant viruses can be generated in packaging cell lines that produce only replication-defective viruses. See Current Protocols in Molecular Biology: Sections 9.10-9.14 (Ausubel et al. , eds.) , Greene Publishing Associcates, 1989.
Specific viral vectors for use in gene transfer systems are now well established. See for example: Madzak et al., J". Gen . Virol . , 73: 1533-36 (1992: papovavirus SV40) ; Berkner et al. , Curr. Top . Microbiol . Immunol . , 158: 39-61 (1992: adenovirus) ; Moss et al. , Curr. Top. Microbiol . Immunol . , 158: 25-38 (1992: vaccinia virus) ;
Muzyczka, Curr. Top . Microbiol . Immunol . , 158: 97-123
(1992: adeno-associated virus) ; Margulskee, Curr. Top .
Mi crobiol . Immunol . , 158: 67-93 (1992: herpes simplex virus (HSV) and Epstein-Barr virus (HBV) ) ; Miller, Curr. Top . Microbiol . Immunol . , 158: 1-24 (1992 :retrovirus) ;
Brandyopadhyay et al . , Mol . Cell . Biol . , 4: 749-754
(1984: retrovirus) ; Miller et al. , Nature, 357: 455-450
(1992: retrovirus); /Anderson, Science, 256: 808-813
(1992:retrovirus) , all of which are incorporated herein by reference.
Preferred vectors are DNA viruses that include adenoviruses (preferably Ad-2 or Ad-5 based vectors) , herpes viruses (preferably herpes simplex virus based vectors) , and parvoviruses (preferably "defective" or non-autonomous parvovirus based vectors, more preferably adeno-associated virus based vectors, most preferably AAV-2 based vectors) . See, e.g., Ali et al. , Gene Therapy 1: 367-384, 1994; U.S. Patent 4,797,368 and 5,399,346 and discussion below.
Furthermore, abnormal or wild-type CD40 receptor- assc iated factor may also be introduced into a target cell using a variety of well-known methods that use non- viral based strategies that include electroporation, membrane fusion with liposomes, high velocity bombardment with DNA-coated microprojectiles, incubation with calcium-phosphate-DNA precipitate, DEAE-dextran mediated transfection, and direct micro-injection into single cells. For instance, an anti-fibrotic polynucleotide encoding an immunosuppressant effective amount of an abnormal CD40 receptor-associated factor may be introduced into a cell by calcium phosphate coprecipitation (Pillicer et al., Science, 209: 1414- 1422 (1980) ; mechanical microinjection and/or particle acceleration (Anderson et al., Proc. Natl . Acad. Sci . USA, 77: 5399-5403 (1980) ; liposome based DNA transfer
(e.g., LIPOFECTIN-mediated transfection- Fefgner et al.,
Proc . Natl . Acad . Sci . USA, 84: 471-477 (1987) , Gao and
Huang, Biochem . Biophys . Res . Com . , 179: 280-285,
1991) ; DEAE Dextran-mediated transfection; electroporation (U.S. Patent 4,956,288) ; or polylysine- based methods in which DNA is conjugated to deliver DNA preferentially to liver hepatocytes (Wolff et al . , Science, 247: 465-468 (1990), Curiel et al., Human Gene Therapy 3: 147-154 (1992) . Each of these methods is well represented in the art. Moreover, plasmids containing isolated polynucleotide sequences encoding CD40 receptor-associated factor polypeptide may placed into cells using many of these same methods.
CD40 receptor-associated factor itself may also be chemically modified to facilitate its delivery to a target cell. One such modification involves increasing the lipophilicity of the CD40 receptor-associated factor in order to increase cell surface binding and stimulate non-specific endocytosis of the polypeptide. A wide variety of lipopeptides, fatty acids, and basic polymers (e.g., tripalmitoyl-S-glycerylcysteil-seryl- serine; palmitic acid; polyarginine) may be linked to an anti-fibrotic polypeptide to accomplish this. See U.S. Patent 5, 219,990, incorporated herein by reference.
Delivery may also be effected by using carrier moieties known to cross cell membranes. For example, an abnormal CD40 receptor-associated factor may be fused to a carrier moiety, preferably by genetic fusion, and the fused construct may be expressed in bacteria or yeast using standard techniques. Thus, polynucleotide sequences encoding abnormal or wild type CD40 receptor- associated factor useful in the present invention, operatively linked to regulatory sequences, may be constructed and introduced into appropriate expression systems using conventional recombinant DNA techniques. The resulting fusion protein may then be purified and tested for its capacity to enter intact target cells and inhibit growth of the target cells once inside the target. For example, recombinant methods may be used to attach a carrier moiety to anti-fibrotic polynucleotide sequences by joining the polynucleotide sequence encoding for abnormal CD40 receptor-associated factor with the polynucleotide sequence encoding a carrier moiety and introducing the resulting construct into a cell capable of expressing the conjugate. Two separate sequences may be synthesized, either by recombinant means or chemically, and subsequently joined using known methods. The entire conjugate may be chemically synthesized as a single amino acid sequence.
Useful carrier moieties include, for example, bacterial hemolysins or "blending agents" such as alamethicin or sulfhydryl activated lysins. Other carrier moieties include cell entry components of bacterial toxins such as Pseudomonas exotoxin, tetanus toxin, ricin toxin and diphtheria toxin. Other useful carrier moieties include proteins which are viral receptors, cell receptors or cell ligands for specific receptors that are internalized and cross mammalian cell membranes via specific interaction with cell surface receptors. Such cell ligands include epidermal growth factor, fibroblast growth factor, transferrin and platelet derived growth factor. The carrier moiety may also include bacterial immunogens, parasitic immunogens, viral immunogens, immunoglobulins, and cytokines.
In one embodiment, purified human immunodeficiency virus type-1 (HIV) tat protein is the carrier moiety. Purified human immunodeficiency virus type-1 (HIV) tat protein is taken up from the surrounding medium by human cells growing in culture. See Frankel et al. , Cell 55: 1189-1193, (1988) ; Fawell et al. , Proc. Natl . Acad. Sci .
USA, 91: 664-668 (1994) (use of tat conjugate) ; and
Pepinsky et al. , DNA and Cell Biology, 13: 1011-1019
(1994) (use of tat genetic fusion construct) , all of which are incorporated herein by reference. See also PCT Application Serial Number PCT/US93/07833, published 3 March 1994 which describes the tat-mediated uptake of the papillomavirus E2 repressor; utilizing a fusion gene in which the HIV-1 tat gene is linked to the carboxy- terminal region of the E2 repressor open reading frame. The tat protein can deliver, for example, abnormal or wild type CD40 receptor-associated factor and polynucleotide sequences into cells, either in vitro or in vivo. For example, delivery can be carried out in vitro by adding a genetic fusion encoding an abnormal CD40 receptor-associated factor- tat conjugate to cultured cells to produce cells that synthesize the tat conjugate or by combining a sample (e.g., blood, bone marrow, tumor cell) from an individual directly with the conjugate, under appropriate conditions. The target cells may be vitro cells such as cultured animal cells, human cells or microorganisms. Delivery may be carried out in vivo by administering the CD40 receptor- associated factor and tat protein to an individual in which it is to be used. The target may be in vivo cells, i.e., cells composing the organs or tissue of living animals or humans, or microorganisms found in living animals or humans. The ADP ribosylation domain from Pseudo onas exotoxin ("PE") and pancreatic ribonuclease have been conjugated to tat to confirm cytoplasmic delivery of a protein. The ADP phosphorylation domain is incapable of entering cells so that cytoplasmic delivery of this molecule would be confirmed if cell death occurs. Likewise, ribonuclease itself is incapable of entering cells so that inhibition of protein synthesis would be a hallmark of intracellular delivery using a tat conjugate.
Chemical (i.e., non-recombinant) attachment of CD40 receptor-associated factor polypeptide sequences to a carrier moiety may be effected by any means which produces a link between the two components which can withstand the conditions used and which does not alter the function of either component. Many chemical cross- linking agents are known and may be used to join an abnormal or wild-type CD40 receptor-associated factor polynucleotide sequence or polypeptide to carrier moieties. Among the many intermolecular cross-linking agents are, for example, succinimidyl 3- (2- pyridyldithio)propionate (SPDP) or N, N'-(l,2- phenylene)bismaleimide are highly specific for sulfhydryl groups and form irreversible linkages; N, N'- ethylene-bis- (iodoacetamide) (specific for sulfhydryl) ; and 1, 5-difluoro-2 , 4-dinitrobenzene (forming irreversible linkages with tyrosine and amino groups) . Other agents include p , p'-difluoro- , m'- dinitrodiphenylsulfone (forming irreversible linkages with amino and phenolic groups) ; dimethyl adipimidate (specific for amino groups) ; hexamethylenediisocyante (specific for amino groups) ; disdiazobenzidine (specific for tyrosine and histidine) ; succinimidyl 4- (N- maleimidomethyl) cyclohexane-1-carboxylate (SMCC) ; m- maleimidobenzoyl-N-hydroxysuccinimide ester (MBS) ; and succinimide 4- (p-maleimidophenyl)butyrate (SMPB) . T h e succinimidyl group of these cross-linkers reacts with a primary amine, and the thiol-reactive maleimide reacts with the thiol of a cysteine residue. See, Means and Feeney, Chemical Modification of Proteins, Holden-Day, 39-43, 1974; and S.S. Wong, Chemistry of Protein Conjugation and Cross-Linking, CRC Press, 1971. All the cross-linking agents discussed herein are commercially available and detailed instructions for their use are available from the suppliers.
In clinical settings, the delivery systems for the abnormal or wild-type CD40 receptor-associated factor polynucleotide sequence can be introduced into a patient by any number of methods, each of which is familiar to persons of ordinary skill. Specific incorporation of the delivery system in the target cells occurs primarily from specificity of transfection provided by the gene delivery vehicle, cell type or tissue type expression due to the transcriptional regulatory sequences controlling expression of the polynucleotide, or a combination thereof. In other embodiments, initial delivery of the recombinant gene is more limited with introduction into the animal being localized by, for example, catheter (U.S. Patent 5,328,470) or stereotactic injection (Chen et al . , Proc . Na tl . Acad. Sci . USA, 91: 3054-3057 (1994) .
Several methods of transferring potentially therapeutic genes to defined cell populations are known. See, e.g., Mulligan, "The Basic Science of Gene Therapy", Science, 260, pp. 920-31 (1993) . These methods include:
1) Direct gene transfer. See, e.g., Wolff et al . , "Direct Gene transfer Into Mouse Muscle In Vivo", Science, 247, pp. 1465-68 (1990) ;
2) Liposome-mediated DNA transfer. See, e.g., Caplen et al., "Liposome-mediated CFTR Gene Transfer To The
Nasal Epithelium of Patients With Cystic Fibrosis", Nature Med. , 3, pp. 39-46 (1995) ; Crystal, "The Gene As A Drug", Nature Med.. 1, pp. 16-17 (1995) ; Gao and Huang, "A Novel Cationic Lipoma Reagent For Efficient Transfection Of Mammalian Cells", Biochem.
Biophys. Res. Comm. , 179, pp. 280-85 (1991) ;
3) Retrovirus-mediated DNA transfer. See, e.g., Kav et al., "In Vivo Gene Therapy Of Hemophilia B: Sustained Partial Correction In Factor IX-Deficient Dogs", Science. 262, pp. 117-19 (1993) ; Anderson, "Human Gene Therapy", Science, 256, pp. 808-13 (1992) ;
4) DNA Virus-mediated DNA transfer. Such DNA viruses include adenoviruses (preferably Ad-2 or Ad-0 based vectors) , herpes viruses (preferably herpes simplex virus based vectors) , baculoviruses, and parvoviruses (preferably "defective" or non- autonomous parvovirus based vectors, more preferably adeno-associated virus based vectors, most preferably AAV-2 based vectors) . See, e.g. Ali, et al., "The Use Of DNA Viruses As Vectors For Gene Therapy", Gene Therapy, 1, pp. 367-84 (1994) ; United States Patent 4,797,368, incorporated herein by reference, and United States Patent 5,139,941, incorporated herein by reference. The choice of a particular vector system for transferring the gene of interest will depend on a variety of factors. One important factor is the nature of the target cell population. Although retroviral vectors have been extensively studied and used in a number of gene therapy applications, these vectors are generally unsuited for infecting non-dividing cells. In addition, retroviruses have the potential for oncogenicity.
Adenoviruses can infect quiescent or terminally differentiated cells, such as neurons or hepatocytes, and appear essentially non-oncogenic. See, e.g., Ali et al., Supra. p. 367. Adenoviruses do not appear to integrate into the host genome. Because they exist extrachromosomally, the risk of insertional utagenesis is greatly reduced. Ali et al., Supra, p. 373. Adeno- associated viruses exhibit similar advantages as adenoviral-based vectors. However, AAVs exhibit site- specific integration on human chromosome 19. Ali et al., supra. p. 377.
The pharmaceutical preparation of the gene therapy construct can consist essentially of the gene delivery system in an acceptable diluent, or can comprise a slow release matrix in which the gene delivery vehicle is embedded. Where the complete gene delivery system can be produced intact from recombinant cells such as retroviral vectors, the pharmaceutical preparation can include one or more cells which produce the gene delivery system.
Effective amounts of the compounds of the invention may be administered in any manner which is medically acceptable. The method of administration may include injections, by parenteral routes such as intravenous, intravascular, intraarterial , subcutaneous, intramuscular, intratumor, intraperitoneal , intraventricular, intraepidural, or others as well as oral, nasal, ophthalmic, rectal, topical, or inhaled. The term "pharmaceutically acceptable carrier" means one or more organic or inorganic ingredients, natural or synthetic, with which the molecule is combined to facilitate its application. A suitable carrier includes sterile saline although other aqueous and non-aqueous isotonic sterile solutions and sterile suspensions known to be pharmaceutically acceptable are known to those of ordinary skill in the art. In this regard, the term
"carrier" encompasses liposomes or the HIV-1 tat protein
(See Pepinsky et al., supra) as well as any plasmid and viral expression vectors. An "effective amount" refers to that amount which is capable of ameliorating or delaying progression of the diseased, degenerative or damaged condition. An effective amount can be determined on an individual basis and will be based, in part, on consideration of the symptoms to be treated and results sought. An effective amount can be determined by one of ordinary skill in the art employing such factors and using no more than routine experimentation.
In preferred methods, an effective amount of the abnormal or wild-type CD40 receptor-associated factor
(CRAF) or polynucleotide sequence encoding the factor
(CRAFl nucleic acid or a nucleic acid sequence encoding
CRAFl peptide) (contained within its attendant vector; i.e., "carrier) may be directly administered to a target cell or tissue via direct injection with a needle or via a catheter of other delivery tube placed into the cell or tissue. Dosages will depend primarily on factors such as the condition being treated, the selected polynucleotide, the age, weight, and health of the subject, and may thus vary among subjects. An effective amount for a human subject is believed to be in the range of about ϋ.l ml to about 50 ml of saline solution containing from about 1 x 107 to about 1 x 1011 plaque forming units (pfu) /ml CD40 receptor-associated factor polynucleotide (CRAFl nucleic acid) containing, viral expression vectors. [U.S. Patent 4,363,877, Recombinant DNA Transfer Vectors, Goodman et al. is hereby incorporated in its entirity by reference.]
Target cells treated by abnormal or wild-type CD40 receptor-associated factor polynucleotide sequences may be administered topically, intraocularly, parenterally, intranasally, intratracheal, intrabronchially, intramuscularly, subcutaneously or by any other means. Target cells to be treated by abnormal or wild-type CD40 receptor-associated factor protein may be administered topically, intraocularly, parenterally, intranasally, intratracheal, intrabronchially, intramuscularly, subcutaneously or by any other means.
The protein compounds of the invention are administered at any dose per body weight and any dosage frequency which is medically acceptable. Acceptable dosage includes a range of between about 0.01 mg/kg and about 500 mg/kg subject body weight. A preferred dosage range is between about 1 and about 100 mg/kg. Particularly preferred is a dose of between about 1 and about 30 mg/kg. The dosage is repeated at intervals ranging from each day to every other month. One preferred dosing regime is to administer a compound of the invention daily for the first three days of treatment, after which the compound is administered every 3 weeks, with each administration being intravenously at about 5 or about 10 mg/kg body weight. Another preferred regime is to administer a compound of the invention daily intravenously at about 5 mg/kg body weight for the first three days of treatment, after which the compound is administered subcutaneously or intramuscularly every week at about 10 mg per subject. The protein compounds of the invention, similarly to the therapeutic nucleotide sequences, may be delivered to tissues in a liposome-encapsulated formulation, or conjugated to carrier moieties such as HIV tat protein. This delivery can be systemic, such as by intravascular delivery, or local. Local means of delivery of liposome-encapsulated compounds of the invention include intratumor or intraorgan injection. It also includes local delivery by catheter, such as intrahepatic delivery into the portal vein, intrarenal or intraprostate delivery via the urethra, intracholecystic delivery via the bile duct, or delivery into various blood vessels of interest, particularly the coronary vessels or sites of vascular stenosis. Targeted delivery may be accomplished by inserting components into the surface of the liposomes or other carrier moieties which confer target specificity. For example, areas of inflammation might be targeted by coating the carrier liposomes with monoclonal antibodies specific for anti-CD40 ligand. Various types of tumors could be selectively targeted by coating liposomes with monoclonal antibodies specific for surface antigens characteristic of the tumor cells. Delivery of the novel polypeptides via liposomes may be particularly advantageous because the liposome may be internalized by phagocytic cells in the treated animal, and because of improved stability. The liposome system may be any variety of unilamellar vesicles, multilamellar vesicles, or stable plurilamellar vesicles, and may be prepared and administered according to methods well known to those of skill in the art, for example in accordance with the teachings of United States Patents 5,169,637, 4,762,915, 5,000,958 or 5,185,154, which are hereby incorporated by reference. In addition, it may be desirable to express the novel polypeptides of this invention, as well as other selected polypeptides, as lipoproteins, in order to enhance their binding to liposome .
The proteins of this invention may be used in the form of a pharmaceutically acceptable salt, suitable acids and bases which are capable of forming salts with the polypeptides of the present invention are well known to those of skill in the art, and include inorganic and organic acids and bases.
The compounds of the invention may be administered as a single dosage for certain indications such as preventing immune response to an antigen to which a subject is exposed for a brief time, such as an exogenous antigen administered on a single day of treatment. Examples of such an antigen would include coadministration of a compound of the invention along with a gene therapy vector, or a therapeutic agent such as an antigenic pharmaceutical or a blood product. In indications where antigen is chronically present, such as in controlling immune reaction to transplanted tissue or to chronically administered antigenic pharmaceuticals, the compounds of the invention are administered at intervals for as long a time as medically indicated, ranging from days or weeks to the life of the subject.
Example 2: Alteration of Expression of CRAFl-encoded Gene Products Are Associated with Hyper-IgM Syndrome (Low or Absent IgG, IgA. IgE) : Target Validation for CRAFl as a target for Immunosuppressive Therapy
Three individuals with non-X linked HIM (Patients A,B and C) that have normal CD40-L expression by the mAb 5c8 (and in the case of patient B by sequence analysis and normal expression of CD40 by the mAb G28-5 were analyzed. Both patients A and B are relatively healthy, since they are 49 and 27 years old, respectively, and have not developed neoplastic disease, nor has either had pneumocystis, opportunistic infections or neutropenia, which are features of HIGMX-1 (37) . Patient C is younger but is relatively healthy.
In vitro analysis of patient A and B's normal B cells showed that their isolated B cells are deficient at responding to anti-CD40 triggering (in the presence of rIL-4) because although these cells secrete large amounts of IgM, they secrete low (barely detectable) amounts of IgG, IgA or IgE in vitro, whereas HIGMX-1 B cells are known to be induced to secrete IgG, A and E by α-CD40 (14-18,20,39) . Patient C has not been evaluated in this assay. Together, these data further suggest that B cell defects may be responsible for the HIM syndrome in patient A and B.
Since NH--terminal truncations in CRAFl act as dominant negatives in cell culture (26) , studies were undertaken to determine whether CRAFl mutations are associated with HIM in individuals with normal expression of CD40-L. Therefore, EBV-transformed lymphoblastoid cell lines were generated from the patients and patient C's mother. The B cell lines from these 3 unrelated patients with HIM (and the mother of patient C) were used to determine the sequence of CRAFl mRNA by RT-PCR. Sets of oligonucleotides designed to sequence CRAFl were selected that amplified four overlapping regions of the CRAFl cDNA.
Sequencing these cloned cDNA fragments revealed little evidence of PCR artifacts in these experiments, consistent with the fact that template mRNA (and later cDNA) was not limiting. The sequences revealed a polymorphism at nt 603 C->T in patients B and C and the mother of C (but not in A) , which alters codon 602-ACG- >ATG and changes aa 128 T->M (which was also found in the cloning of CRAFl by other groups (27,28) . Therefore, the PCR cloning and sequencing appeared to have high fidelity and not to have been the result of cross-contamination. From the DNA sequences cloned, consistent mutations were not identified that could relate CRAFl defects to HIM. However, the lack of mutations suggested that CRAFl splicing defects could alter signaling.
Analysis of CRAFl peptides in HIM patients Analysis of CRAFl encoded peptides has recently become possible because of the availability of anti-CRAFl antisera. Therefore, this antisera was used to determine if protein products of the potentially mutated alleles are present in cells from these individuals. A rabbit antiserum generated to the NH2-terminus of the CRAFl peptide was used to perform immunoprecipitation of metabolically labeled Ramos cells, Ramos/pCEP/CRAFl and EBV-transformed B cell lines [pCEP is an expression vector available from Invitrogen] . Several bands are specifically immunoprecipitated by the anti-CRAFl antisera, including major bands that migrate at 70 kDa and 60 kDa. The intensity of the 60 kDa band is strongly increased in lysates from Ramos/pCEP/CRAFl cells, which suggests that this band represents the peptide product of the CRAFl-a transcript and which is consistant with the predicted molecular weight of a 568 aa peptide. The expression of both the 60 kDa band and the 70 kDa band is greatly increased in the EBV transformed cells relative to the intensity of these bands in Ramos controls suggesting that EBV transformation increases the expression of CRAFl peptides and which is consistant with the observation that EBV upregulates CRAFl mRNA in BJAB cells (27) .
Immunoprecipitation of metabolically labelled EBV- transformed B cell lines from a normal individual and from the patients A and B was performed. In all three cell lysates, anti-CRAFl antisera immunoprecipitates major bands that migrate at 70 kDa and 60 kDa. (The intensity of the 60 kDa band is strongly increased in lysates from Ramos/pCEP/CRAFl cells, which suggests that this band represents the peptide product of the CRAFl-a transcript.) However, this patient's B cell lysates contain a unique, approximately 77 kDa band (p70 or p77) , that is not observed in the other EBV transformed cell lines or in the Ramos transfectants analyzed. Similar to the immunoprecipitates from patient B's cells, the lysates from the patient A cell line also contains the 60 kDa band, suggesting that if this patient has a mutated allele, a normal allele may also be present. It is unknown if the predicted 70 kDa peptide is relatively unstable or if some other process (potentially compensatory) is occurring in these cells, that would result in the 77 kDa (p70 or p77) band by a complex process, such as alternative splicing to delete a exon 3 that contains an in-frame termination codon. The Western blot data in Figure 5 suggests that p70 may not be rapidly degraded, since patient A has p70 peptide with a low rate of p70 synthesis.
Western blotting can be used to provide further evidence that the 30 kDa band that is specifically detected in patient B's cell lysates is a product of the CRAFl gene or whether it represents a co-precipitating peptide that is unique to cells from this patient. (However, the fact that the 30 kDa band is predicted by the cloning data strongly suggests that this peptide does in fact, represent the COjjH-terminal truncation.)
Characterization of the functional effects of inhibitory cDNAs of the p55 type in tumor cell models of CD40- triggering of B cells
To test whether carboxy terminal truncated proteins operate as dominant negatives in cultured cell lines, stable transfectants of Ramos that express the 1-171 amino acids of p55 and the 1-258 amino acids of p55 were generated. Three clones of stable transfectants of both pCEP/CRAFl-PtA and pCEP/CRAFl-PtB in Ramos cells have been generated, and confirmed the presence of plasmid encoded CRAFl mRNA has been confirmed by Northern analysis. As controls for this experiment, cDNA encoding full length 568 aa CRAFl was cloned into the pCEP expression vector (Invitrogen) and expressed this clone in Ramos. The cell surface expression of CD23 and CD80 on Ramos/pCEP/CRAFl transfectants shows that CD23 expression is not upregulated (relative to Ramos/pEBVHIs/lacZ controls (Figure 3) . These data indicate that expression of full length CRAFl does not induce the phenotype of a constitutively CD40-activated B cell, at least with respect to CD23 and CD80. Next, the responses of these transfectants to CD40 triggering was studied. In these experiments, CD40-triggering was induced by coculture with 293/CD40-L cells (or control 293/CD8 cells, not shown) . In response to CD40 triggering with 293/CD40-L cells, Ramos/pCRAFl cells have normal responsiveness with respect to upregulation of CD23 or CD80 or ICAM1. In functional experiments, the Ramos cells over-expressing the clones were triggered with 293/CD40-L* cells and the expression of CD23 and CD80 was measured by two-color FACS. Interestingly, despite the modest expression of plasmid mRNA in these cells, the transfected clones were deficient at upregulating CD23 in response to stimulation with 293/CD40-L* cells relative to control Ramos cells or Ramos cells expressing full length CRAFl. In this experiment, upregulation of CD80 by CD40 triggering was normal relative to control Ramos cells and to Ramos cells expressing full length CRAFl. The deficiency in CD23 upregulation has also been observed in non-transformed B cells from patients with non-CD40-L related HIGM (21) . These data provide a molecular mechanism by which CO^-truncated CRAFl mutants result in HIM.
It can be determined whether the functional phenotype of these cells corresponds to the phenotype of the patients altered alleles expressed in Ramos cells as described above, however, it is interesting in this respect, that HIM patients with normal CD40-L have been described to have a deficiency in CD23 upregulation (37) and Patient B was one of the individuals in that study.
Characterization of the roles of CRAFl in B cell signaling
Understanding of the role of CRAFl in CD40 signalling has been extended by studying the functional deficit in Ramos cells stably expressing pEBVHis/C26 ("dominant negative) or pEBVHis/lacZ ("control") constructs. In experiments similar to those described for assessing CD23 upregulation, Ramos transfectants were co-cultured with 293/CD40-L cells or control 293/CD8 cells and the expression of CD80(BB1-B7) and ICAM1 was measured by 2- color FACS. The CD40-L induced upregulation of CD80 (40) was substantially inhibited by C26 expression although this inhibition is not as potent as the effect of C26 expression on CD23. These data indicate that CD40-mediated upregulation of CD80 (which has been shown to correlate with the induction of co-stimulatory activity by B-CLL cells (see above) ) appears to depend in large part on CRAFl signaling. CD40 triggering also induces upregulation of CD54 (ICAM1) (40) and homotypic aggregation, but these effects are not inhibited by overexpression of the CRAFl dominant negative C26-1 fusion protein. These data suggest that CD40 signaling involves at least one other component, or that the induction of ICAM1 upregulation is less sensitive to CRAFl inhibition. DISCUSSION:
These studies suggest an interpretation of CRAFl signaling. The complete predicted aa sequences of human and mouse CRAFl are highly homologous and reveal a Zn** ring domain, a Zn** finger domain, a coiled-coiled domain and importantly, that the -CO^-terminal domain that binds the CD40 cytoplasmic tail is homologous to two recently identified proteins, "TNFα Receptor-Associated Factors" 1 and 2 (TRAF-1 and TRAF-2) that form a complex with the cytoplasmic tail of TNFRαll (41) . Thus CRAFl peptide is a critical signaling factor in CD40 mediated responses and may transmit CD40 signals to the nucleus. More consistent with aggregation and less with proteolytic processing.
After the generation of stable transfectants expressing these constructs, the phenotype of the transfectants is analyzed (to determine whether constitutive activation of CD23 and/or CD80 expression is present) or CD40- triggered functional assays are performed to analyze the potential dominant negative effects of these constructs. Analysis of constitutive activation may be carried out by evaluating and detecting relative amounts of tumor cell death. One possible outcome of these experiments is that overexp ession of the Zn ring and finger domains in isolation from other domains, will result in constitutive activation of Ramos cells (i.e., constitutive high expression of CD23 and CD80) . This would be taken to suggest that CD40-signaling may activate CRAFl by proteolysis which would liberate the DNA binding domain. Since the full length CRAFl is not constitutively activating, this finding would suggest that other portions of the molecule (e.g., the coiled- coil domain) might normally retard the translocation of CRAFl Zn ring/finger domains to the nucleus. This type of signaling has been described in the signaling of the sterol regulatory element-binding protein (SREBP-1) ( 42 ) .
Another possible outcome is that no domain is constitutively activating alone, but that, for example, the coiled-coil domain alone in a fusion protein, may function as a dominant negative (i.e., similarly to C26) . These data would be consistent with a model in which CRAFl signaling is primarily mediated by oligomerization of CRAFl molecules, either to each other or in heteromeric complexes, this type of oligomerization is reminiscent of the JAK/STAT signaling system described by in interferon signaling (43) . Moreover, this result would be interpreted in light of the results of experiments described below which ask whether CRAFl is constitutively associated with CD40 or whether CD40 aggregation by trimeric CD40-L initiates the oligomerization of CRAFl and potentially, whether such oligomerization of CRAFl may result in its association with other signaling molecules, in analogy with the JAK/STAT system. Such results would also lead to re-interpretation of the mechanism by which the C26 peptide mediates its dominant negative activity. In this regard, how C26 mediates its dominant negative effect is under study. The simplest model to explain the dominant negative effects of C26 is that the C26- encoded fusion protein binds to the CD40 cytoplasmic tail and prevents the binding of full length CRAF molecules. However, the C-TRAF domain of C26 also mediates self-self oligomerization (26) and potentially, the C26 peptide may interfere with the oligomerization of endogenous CRAFl molecules to mediate its dominant negative effects.
CD40 is a cell surface receptor for the T helper effector molecule, CD40-L (T-BAM, gp39, TRAP) and this interaction is essential for B cell selection and differentiation in vitro and in vivo. A protein that binds to the cytoplasmic tail of CD40 termed "CD40 Receptor Associated Factor 1"(CRAFl) has been identified. Stable overexpression of the 240aa carboxy terminus of CRAFl as a fusion protein (C26) in Ramos 2G6 B cells inhibits the CD40-dependent induction of CD23 expression
(i.e. results in a functional "dominant negative") . To determine if CRAFl is involved in other CD40 effector functions, Ramos B cells expressing the C26 fusion protein or control (expressing lacZ) were stimulated with anti-CD40 mAb (G28-5) and assessed for their ability to be rescued from Fas (CD95) -mediated apoptosis
(Wright-Giemsa staining) , to undergo homotypic aggregation (light microscope) or to upregulate CD54
(ICAM) or CD80 (B7/BB-1) (FACS) . Similar to its effects on CD40-mediated upregulation of CD23, C26 inhibits anti-CD40 mediated rescue from Fas-mediated apoptosis and inhibits anti-CD40 mediated CD80 upregulation. However, C26 does not affect CD40-mediated CD54 upregulation nor homotypic aggregation, suggesting that the CD54 upregulation pathway is either less sensitive to C26 inhibition or possibly that CD40 has alternative (non-CRAFl) mediated signaling. Together, these data suggest that CRAFl mediates the CD40 signals for rescue from apoptosis and upregulation of CD80, however, the CD40 signals for inducing ICAM are unresolved.
CD40-L is known to have a different role from CD95 in germinal center biology because mutations in CD40-L impair germinal center formation as manifest in humans that have absent or mutant CD40-L protein expression (X- linked, hyper-IgM syndrome (HIGMX-1) or mice with targeted disruptions of CD40-L or CD40. The lack of germinal centers in HIGMX-1 is associated with extensive IgM+ B cell infiltration of tissues, particularly in the GI tract (11,13-18,20), which may relate to the predisposition of HIGMX-1 patients to develop polyclonal B cell pseudolymphomas (11,13) . These data suggest that apoptosis in germinal centers play important roles in limiting IgM* B cells and to the extent that CD95 represents a limiting step in mediating B cell apoptosis in germinal centers, these data suggest that CD95 normally regulates B cell homeostasis and limits B cell transformation. Although the role of CD40-L in germinal center formation is elucidated by the lack of germinal centers in HIGMX-1, this syndrome does not address the role of CD40-L on T cells in germinal centers.
EXPERIMENTAL MATERIALS AND PROCEDURES Monoclonal Antibodies
The mAb 5c8 (anti-CD40-L) has been described (1) . The following mAb were produced from hybridomas available from the American Type Culture Collection (Rockville, MD) : 0KT8 (anti-CD8), DA4-4 (anti-IgM) and W6/32 (anti- MHC class I) . These mAb were purified from ascites fluid on protein A (Biorad, Rockville Center, NY) or protein G columns (Pharmacia, Upsula, Sweden) . Leu-16 (Anti-CD20) mAb conjugated to flourescein and Leu-17 (Anti-CD38) mAb conjugated to PE were purchased from Becton Dickinson (Mountainview, CA) . BB20 (anti-CD40) was purchased from Biosource International (Camarillo, CA) .
Cell Lines
The human B cell lymphoma clone RAMOS 2G6.4CN 3F10 (Ramos 2G6) is available from ATCC. 293/CD8 is a human kidney tumor cell line that is stably transfected with CD8 as described (10,50) . Stable CD40-L* clones of 293 cells (293/CD40-L) were generated by electroporation of a cDNA that encodes CD40-L (pCD40-L/SpeI) and cloning of transfectants that express surface CD40-L by mAb 5c8 binding. To generate pCD40-L/SpeI, a CD40-L cDNA (pTBAM described in Covey et al . (10)) was used as template for PCR amplification using a 5'- oligonucleotide (oCD40-L/SpeI:5' -GCA gCT AGC CAC AGC ATG ATC GAA ACA TAC AAC CAA ACT AGT CCC CGA TCT GCG-3' ) (Seq
I.D. No. ) that altered the CD40-L sequence of the amplified product to create a Spe I site at position 25, a Nhe I site at position -12, and to append the putative 5'-UT Kozak sequence (6) . The 3' oligonucleotide corresponds to pCCD40-L 616-633 (oCD40-
L 6__-616: 5' ~CTT TAG GCA GAG GCT GGC-3') (Seq I.D. No. ) .
The PCR product generated was digested with Nhe I and Hind III, cloned into the expression vector pREP4 (Invitrogen, San Diego, CA) and its sequence was confirmed by automated sequencing. The CD40-L coding region was completed by insertion of the 3' end of the pTBAM cDNA as a Hind III -Wot J fragment from pCCD40-L, yielding pCD40-L/SpeI .
Isolation of Tonsillar B lymphocytes
Tonsil B cells were obtained from fresh surgical specimens after tonsillectomy. The lymphoid tissue B cells were obtained by mincing tissue specimens and passing them through a metal screen followed by ficoll- hypaque (Sigma, St. Louis, MO) centrifugation. B cells were derived from the population of cells that did not pellet through Ficoll-Hypaque after one round of rosetting with neuraminidase-treated sheep erythrocytes. Tonsillar B cells were further purified by density centrifugation. Cells were fractionated into high (resting) and low (germinal center CD38 enriched) density cells in a discontinuous 30%/50%/100% percoll gradient by centrifugation at 2300 rpm for 12 min. High density cells were obtained from the 50%/100% interface and low density cells from the 30%/50% interface (33 , 51) .
Cytofluorographic analysis of Tonsillar B cells
Approximately 105 cells were incubated with saturating concentrations of the indicated mAbs for 45 min at 4° C in the presence of 80 μg/ml heat aggregated IgG
(International Enzyme, Fallbrook, CA) . Cells were washed to remove unbound antibody before incubation with F(ab)2 goat anti-mouse Ig secondary antibody coupled to fluorescein (Jackson Immunoresearch, Westgrove, PA) . Two color FACS (Fluorescence Assisted Cell Sorter) analysis involving both direct and indirect antibody staining was accomplished as above for indirect antibody staining except that cells were washed prior to incubation with conjugated antibody. Fluorescence intensity was measured on a FACScan cytofluorograph (Becton Dickinson) using Consort 30 software.
Assays of Anti-IgM and anti-CD95 induced apoptosis
Ramos B cells (3 X 106) or freshly isolated low density or high density tonsillar B cells (5 X 106) were added to each well of sterile 12 well tissue culture plates
(Costar, Cambridge, MA) and incubated with media alone
0.5 μg/ml anti-CD95 mAb (APO-l/huFcγl) or control chimeric anti-CD4 (mAb M-T412/huFcγl) , 5 μg/ml anti-IgM or 5 μg/ml or 0.5 μg/ml of control anti-Class I (mAb W6/32) as indicated in figure legends. In addition, wells contained either media, 0.5 X 106 TBAM/293 cells or CD8/293 cells in the presence or absence of mAbs anti- CD40-L (5c8) or control mAb (W6/32) in a final volume of 1 or 2 ml. Cultures were incubated for either lOh or 14h (anti-CD95 induced apoptosis) or 36 h (anti-IgM induced apoptosis) before cells were harvested and analyzed for apoptosis by cell morphology and DNA fragmentation into nucleosomal units.
Determination of Apoptosis by Cell Morphology
Low density tonsillar B cells or Ramos 2G6 cells were treated as indicated above. Cells were washed and 1 X 105 were cytospun onto microscope slides using a Cytospin 3 (Shandon, Cheshire England) . Cells were stained for two minutes with Wright-Gie sa (Sigma, St. Louis, MO) , rinsed with distilled water and dried before observation by light microscopy (Olympus CK2) . Cells were scored as viable (non-apoptotic) if they maintained an intact cell membrane and nucleus and did not display membrane blebbing, condensed cytoplasm, pyknotic nuclei or other characteristics of an apoptotic cell (52) . Photographs of representitive cell populations were taken by an Olympus 0M-2S camera.
Determination of Apoptosis by DNA fragmentation and Cell Viability DNA fragmentation was assessed by a modification of Benhamou et al. (53) . Treated cells were washed twice in HBSS and lysed in 400 μl of buffer containing 10 mM EDTA, 200 mM NaCl, 0.1 mg/ml Proteinase K, 0.5% SDS, and 50 mM Tris-HCl (pH 8.0) . After lh incubation at 50° C, lysed cells were subjected to phenol-chloroform extraction. Genomic DNA was precipitated by the addition of 2 volumes of 100% ethanol and was removed using a sterile pipette tip. Fragmented DNA was precipitated after the addition of 1/10 volume of 3 M NaOAc (pH 7.2) and incubation at -70° C for 2-5 h. Precipitated DNA was then washed with 70% ethanol, dried, and resuspended in 20 μl of RNase buffer consisting of 15 mM NaCl, 10 mM Tris-HCl (pH 7.5) and 5 μg/ml RNase A. After incubation at 50° C for 1 h, DNA was electrophoresed on a 1.5% agarose gel at 80 V for 1-
3 h and stained with ethidium bromide. This method allows for the isolation of fragmented DNA only and therefore can be used to assess the relative level of apoptosis in the B cell population when total sample is loaded to each well, since each sample contains an equivalent number of tonsillar or Ramos B cells and 293 cells are resistant to CD95 induced apoptosis.
Primers for PCR The oligonucleotide primers used in these experiments are are designated "o", followed by "CR" for CRAFl, followed by "f" or "r" for forward and reverse respectively and then the nucleotides that they correspond to with the numbering of the CRAFl nucleotide sequence of clone IHb that is deposited in Genbank U21092) . These oligos include: oCRf (127-144) (5' -AgC AgA ACg CTg Cgg ACC) (Seq. I.D. No. ) , oCRr(675-658) (5' -
CAg TCA ggA CgC ACA CAT) (Seq. I.D. No. ) , oCRf(486-
503) (5'-CgT gTC AAg AgA gCA TCg) (Seq. I.D. No. ) , oCRr(1091-1074) (5' -gCA AAC TTT gTA TgC TCT) (Seq. I.D. No. ), oCRf (902-919) (5' -CCC AgC ACC TgT AgT TTT) (Seq. I.D. No. ) , oCRr (1450-1433) (5' -ggT CTC CAg gAC CTg gAA) (Seq. I.D. No. ) , oCRf (1164-1181) (5' -TCC TTC ATT
TAC AgC gAg) (Seq. I.D. No. ) , oCRr(2119-2102) (5' -gAA gTg Tgg CTA gTC TAT) (Seq. I.D. No. ) , oCRf(550-
567) (5'-ggC TCT TCA gAT CTA Ttg) (Seq. I.D. No. ) , oCRr(144-126) (5' -ggT CCg CAg CgT TCT gCT C) (Seq. I.D.
No. ), oCRr(213-197) (5'-ggA AAg Agg AgT TCT Cg) (Seq.
I.D. No. ) and oCRr(289-272) (5' -gTC AgT gTg CAg CTT
TAg) (Seq. I.D. No. ) .
The four overlapping cDNA fragments were amplified by RT-PCR in which the RT reaction was primed with oCRr (2119-2102) . The following pairs were found to produce the expected products in RT-PCR on mRNA from a control EBV transformed B cell line: including (1.) oCRf (127-144) /oCRr(675-658) yields product (127-675) ,
(2.) oCRf (486-503) /oCRr (1091-1074) yields product (486-
1091), (3.) oCRf (902-919) /oCRr(1450-1433) yields product
(902-1450) and (4.) oCRf (1164-1181) /oCRr (2119-2102) yields product (1164-2119) . The four overlapping regions in each of the patients (including those of the mother of patient C) were amplified, the amplified fragments were isolated and cloned in the TA cloning system (pCRII, Invitrogen) and the inserts from these plasmids were sequenced in both directions.
To generate cDNAs containing the mutations from patient A and B, the PCR product generated by oCRf (550-567) and oCRr (1091-1074) , which yields product (550-1091) was cloned into pCRII (Invitrogen) and digested with Bgl II (which cuts within oCRf (550-567) ) and EcoRl (which cuts in the polylinker of pCR-II and generates similar fragments (except for the patient A or B sequence transitions) independently of the fact that the PCR products from A and B were initially cloned into pCRII in different orientations. The Bglll/EcoRI fragments of patient cDNAs were ligated into pCRAFl/Bluescript digested with Bgl II/Eco RI to yield fragments that contain the premature termination codons of patient A and B. The cDNAs encoding the full coding sequence of the patients were then digested with Not I/Xho I and ligated into pCEP/CRAFl and pEBV/His/CRAFl.
Example 3; CRAF-1 Isoforms with Zinc Finger Deletions One isoform of CRAF-1 peptide is a 568 aa signaling protein that interacts with the cytoplasmic tail of B cell surface molecule CD40 and mediates a variety of T- dependent effects on B cell activation and differentiation. CAP-1, which is a cDNA related to CRAF-1 nucleic acid, is similar to a CRAF-1 nucleic acid except for a 75 nucleotide deletion in a region which, in a CRAF-1 nucleic acid embodiment provided for herein, encodes five zinc finger-like domains. To determine whether alternative mRNA splicing from a common CRAF-1 gene accounts for this difference, the structure of human CRAF-1 nucleic acid mRNA and genomic DNA was analyzed using RT-PCR (reverse transcriptase - PCR) and long-template PCR amplification, respectively, followed by subcloning and sequence analysis. In addition to a CRAF-1 nucleic acid and CAP-1 (del aa218-242) encoding transcripts, a third mRNA species was identified that predicts a peptide with a larger (52 aa) deletion in this region (del aal91-242) . Analysis of the genomic structure of a CRAF-1 gene in this region identified exons that encode aal91-217 and aa218-242. These exons are separated from each other by a 3.5 kB intron and from the adjacent 5'- and 3'- exons by 9.5 kB and 3.5 kB introns, respectively. The loss of these exons in the two smaller transcripts suggests that these deletions arise by alternative mRNA splicing. The location of these deletions within the zinc finger-like region of CRAF-1 nucleic acid predicts the loss of two or three zinc fingers, in the CAP-l(del aa218-242) and del aal91- 242 forms, respectively.
In other proteins which contain zinc finger domains, such zinc finger domains interact with other proteins, RNA or DNA. Together, these data suggest that differential splicing modulates CRAF-1 peptide signaling by generating a variety of CRAF-1 peptide isoforms which differentially interact with other constituents of the cytoplasmic signaling apparatus.
Enhancing Alternative Splicing Because alternative splicing removal of particular exons results in inhibitory CRAFl isoforms, agents that drive such alternative splicing are expected to have beneficial effects similar to mAb 5c8 treatment (See U.S. Patent No. 5,474,771, issued December 12, 1995) . Such agents include gene therapy constructs that encode elements of the splicing appratus. These constructs may be used singly or in combination. For example, certain elements of the splicing complex that have effects on RNA splicing generally, may be over-expressed alone, or in combinations with other elements of the splicing complex that has specific targeting effects on the CRAF-1 RNA splicing. These elements include both gene therapy constructs that encode protein elements of the splicing complex as well as others that encode RNA elements of the splicing complex. Activity of gene therapy constructs comprising the whole proteins or whole RNA molecules that participate in RNA splicing allows the identification of smaller constructs containing minimal essential elements of these nucleotide segments, for example steroid-like molecules. Furthermore, the identification of the minimal elements leads to the identification of smaller organic molecules that have the essential chemical features and biological activity of the larger DNA elements (enhancing the RNA splicing that generates CRAF-l isoforms by deleting a particular the RNA of a particular exon) .
Such agents include preferentially target the splicing of the particular exon which is removed. Such agents include cytokines and small organic agents that induce cell differentiation or activation.
Specific examples of elements of the splicing apparatus which can be used to enhance splicing in the method of this invention include small nuclear RNAs (snRNAs) sch as Ul, U2, U3, U4, U5 and U6. Because these snRNAs exist stably complexed with certain nuclear proteins, splicing can also be enhanced using small nuclear ribonucleoproteins (snRNPs) . (See Watson, et al .
Molecular Biology of the Gene, 4th ed.
(Benjamin/Cummings : Menlo Park 1987) pp. 640-644.) . A number of splicing factors or enhancers of pre-RNA splicing have been identified in Drosophila, including Transformer 1 (Tral) , Transformer 2 (Tra2) , SF2/ASF, SC35, Srp20, Srp55, Srp75, U2AF65, and U2A*F . (See Amrein, et al. Cell (1994) 76:735-746; Heinrichs, et al . EMBO J. (1995) 14: 3987-4000; Lynch et al . , Genes & Development (1995) 9:284-293) . Factors which enhance RNA splicing generally, or CRAFl-specific splicing are used to enhance splicing in the zinc-finger region of CRAFl.
Example 4:Chromosomal Localization, Genomic Structure, And Identification of Alternatively Spiced mRNAs Of Human TRAF-3
TRAF-3 (CRAF-1, LAP-1, CD40bp) is a cytoplasmic signaling molecule that interacts with the cytoplasmic tail of CD40 and transduces contact dependent signals for B cell activation. The gene for TRAF-3 was characterized by FISH (fluorescence in situ hybridization) and by radiation hybrid mapping and found to be located at chromosome 14q32.2, approximately 1 Mbase centromeric to the Ig heavy chain locus. TRAF-3 was further characterized by genomic PCR and sequencing genomic λ-phage and PI clones. TRAF-3 is encoded by 10 exons which roughly correspond to protein domains predicted by the TRAF-3 cDNA. Interestingly, a variety of TRAF-3 cDNA species were identified which are generated by alternative mRNA splicing of distinct exons. Many of these species predict novel TRAF-3 peptides which vary in critical structural regions of this signaling protein.
INTRODUCTION
TRAF-3 (CRAF-1, LAP1, CD40bp) is a 568 amino acid cytoplasmic signaling molecule that plays an important role in the transduction of signals from the CD40 receptor in B cells. TRAF-3 has also been shown to bind the cytoplasmic domain of at least one other membrane receptor, the receptor for lymphotoxin-β, and TRAF-3 mRNA is expressed by cells of many lineages. Furthermore, in addition to physiologic signaling, TRAF- 3 may also play a role in EBV-driven B cell proliferation and immortalization, by binding EBV latent membrane protein-1.
TRAF-3 is a member of the TNFα-receptor associated factor family "TRAF family" of signal transducing molecules on the basis of homology in the carboxy terminus of family members TRAF-1 and TRAF2. These signaling molecules contain a COOH-terminal TRAF subdomain (TRAF-C) that mediates protein:receptor binding. In addition to the TRAF-C domain, sequence analysis of the TRAF-3 protein has revealed four other potential domains, including a zinc ring, a complex composed of five atypical zinc fingers, a coiled-coil (isoleucine zipper) structure, and an NH3-terminal (TRAF-N) domain. In other molecules, zinc rings, zinc fingers, and coiled-coil structures mediate protein- protein interactions. These structural data suggest interactions by which TRAF-3 may transmit CD40 signals, for example by interacting with other cytoplasmic proteins, including other TRAF-3 molecules or TRAF family members. Therefore, the distinct structural domains of TRAF-3 may play distinctive roles in TRAF-3 function.
Interestingly, several lines of evidence have suggested that these domains may be differentially expressed in different TRAF-3 isoforms. For example, in the deposited sequences for murine and human TRAF-3, there are nucleotide sequences which are related by the inclusion or exclusion of distinct gene elements, consistent with alternative splicing, in the portion of the TRAF-3 cDNA that encodes 5'-UTR (untranslated region) DNA. Furthermore, one TRAF-3 species (called IHb) contains an open reading frame that extends upstream from the start site of 568 aa TRAF-3. Another species of TRAF-3 was reported by Reed, and termed CAP- 1, which predicts a peptide with a 25 aa deletion in the zinc finger complex.
The chromosomal localization and genomic structure of TRAF-3 was determined, in order to understand the structure and genesis of TRAF-3 mRNA. Various isoforms of TRAF-3 were identified which suggest that alternative splicing of TRAF-3 mRNA may generate distinct TRAF-3 peptides. Such isoforms may play different roles in the signaling function of TRAF-3, and may thus represent a mechanism for the regulation of TRAF-3 in B cells.
CHROMOSOMAL LOCALIZATION OF TRAF-3
To identify the chromosomal localization of TRAF-3, fluorescence in situ hybridization (FISH) analysis of human fibroblast metaphase spreads was undertaken using genomic λ phage clone #6 as a probe. This probe bound specifically to the telomere of the long arm of human chromosome 14, at position 14q32.
Since this region is known to contain the human immunoglobulin heavy chain locus, and since this locus contains a well-characterized breakpoint in Ramos cells, a non-EBV infected Burkitt's tumor cell line, localization of TRAF-3 with respect to this chromosomal landmark was performed. Two-color FISH was performed on metaphase chromosomes from Ramos cells using the TRAF-3 probe and a chromosome 14 telomere probe. The two probes bound in very close proximity on the normal chromatid, within an estimated distance of 1 Mb. Only the TRAF-3 probe, however, bound to the ho ologue of chromosome 14 that had undergone breakage, whereas the chromosome 14 telomere probe bound to chromosome 8, consistent with the translocation of this telomere to chromosome 8 in Ramos.
Taken together, these data indicate that the TRAF-3 gene is located centromeric to the Ramos breakpoint on 14q32. The close physical proximity of the two probes further suggested that TRAF-3 and this breakpoint, [which is within the Cμ switch region in the immunoglobulin heavy chain locus] are located within one Mb of each other, an estimate that was confirmed by a PCR-based screening assay of a somatic cell hybrid panel. From this screen, the TRAF-3 locus lies within 3.5 cR (approximately 1 Mb) of framework markers FB19F11 and WI-9179 on the Whitehead radiation hybrid database.
CHARACTERIZATION OF THE GENOMIC STRUCTURE OF TRAF-3 Isolation and Characterization of TRAF-3 cDNA clones
A Raji cDNA library was screened with C26, a cDNA probe that represents the terminal 1271 nt of the TRAF-3 open reading frame. A second screen was performed with Notl- SacI, a probe which represents the first 447 bp of IHb. These screens revealed unexpected diversity in the 5' portion of TRAF-3 when compared with IHb, the full- length TRAF-3 sequence which was initially cloned from this library. IHb contains 206 bp of the TRAF-3 5'- untranslated region (called exon 3) as well as the entire TRAF-HI open reading frame. One clone, lb, was identical to IHb except for the inclusion of an 139 bp exon, which was called exon 3. This exon contains a stop codon in the reading fram of exon 4 which contains the p55 translational start site (IHb nt 224; Figures 1A-1P, nucleotide 679) . Another clone, 2-1, contained exon 3, and a third unique exon, at least 77 bp long, which precedes exon 3, and was called the product of exon 1. Several lines of evidence suggest that these diverse mRNA species were represented in mRNA and not artifacts of the cloning procedure. RT-PCR, for example, revealed the appropriate products encoding IHb-like, lb-like and 2-1-like species. Moreover, 5'- RACE (Rapid Amplification of cDNA Ends) revealed the identical arrangement of exons, but did not reveal upstream sequences that were distinct from those contained in the characterized cDNA clones. These data suggested that alternative splicing of distinct exons resulted in the 5' variation seen in these three TRAF-3 cDNA clones.
Isolation and Characterization of TRAF-3 Genomic clones
From a human genomic phage library (referred to PI or as pAC clones) three clones (#4, #6, and #9) that hybridized with cDNA probe Hindi-Hindi (IHb 606-1003) were isolated. These clones were characterized by restriction digestion with [Notl and EcoRI] and by PCR mapping. Each phage clone contained an insert of about 20 kb. Two of these clones (#4 and #9) were found to be overlapping but distinct, containing the 3' end of the gene [nt 981-2437 on IHb cDNA] ; the third clone, #6, was found to encode the 5' end of the gene [nt 207-793 on IHb cDNA] . The gap from nt 794-981 is covered by pAC clone #167.
To further characterize the genomic structure of TRAF-3, a human genomic PI (or pAC) artificial chromosome library was screened with two different TRAF-3 genomic probes, ff7gen-fr8gen and pstlc-r2glx. A 124 kb PI clone (pAC clone #167) (ATCC Accession No. ) that hybridized to both probes was isolated and characterized by genomic PCR. This clone was found to contain DNA that encoded the entire open reading frame of human TRAF-3.
Linking 5'-UTR to the TRAF-3 coding region
The TRAF-3 5'-UTR was not contained on the most 5' λ-fix clone (clone #6) or on PI clone #167 by Southern blotting with probe CE, a 193 bp fragment which contains part of the TRAF-3 5'-UTR including exon 3. Therefore, the genomic library was re-screened with this probe, and a single PI clone [#34] (pAC clone #34, ATCC Accession No. ) was isolated. Restriction digestion of
PI clone #34 with EcoRI identified a 3.8 kb genomic restriction fragment that hybridized to the CE probe. Furthermore, a 6.0 kb EcoRI fragment was identified that hybridized to zfl, a 25 bp end-labeled oligonucleotide primer that represents part of exon 1. A third EcoRI fragment, 7.0 kb long, hybridized to probe Notl-Smal, which represents the 5' half of exon 2. All three genomic fragments were subcloned into Bluescript and sequenced in both directions, using exon-specific primers, confirming these data.
Although these studies identified genomic DNA that encodes the 5'-UTR, none of these clones hybridized with probes that contained the coding region of TRAF-3. Genomic PCR between exon 3 and the TRAF-3 coding region using uncloned DNA as a template did not generate a reaction product. Similarly, genomic PCR between each of the exons in the 5'-UTR, using both uncloned DNA and PI clone #34 as template, did not generate a reaction product. It is therefore estimated that the separation between exon 3 and exon 4 (which contains the start site of p55) between the exons is at least 28 kilobases. The separation between exon 2 and exon 3 is about 54.5 kb.
The CRAF exons were flanked on the 5' -side of ;AC #34 by ORF (D14S72) and on the 3' -side of pAC #167 by EST (SGC 30775) , confirming the chromosomal location determined by FISH and radiation hybrid mapping and which indicated that pAC #34 is centromeric to pAC #167 and that the transcriptional orientation of the CRAFl gene is centromeric to telomeric, or in the reverse orientation of the Ig heavy chain gene locus (transcriptional orientations are indicated by arrows in Figure 6.
Establishing exon/intron boundaries
Relevant regions of genomic clones (λ fix clones #6 and #9 and pAC clones #167 and #34) were sequenced in both directions using oligonucleotide primers developed from TRAF-3 cDNA clones lb, IHb, and 2-1 [Tables 1 and 3] . Comparison between genomic and cDNA sequence data permitted the definition of exon/intron boundaries for each of the TRAF-3 (p55) coding exons as well as the 3' borders of exons 1, 2 and 3. The 3' border of exon 1 was determined from the spliced species which represented an exon 1,3 product. However, the 5' border of exon 2 could not be established from cDNA's obtained, which did not include an example of an exon 1, 2, 4 product, presumably because of the high G-C content of this region. Therefore, the 5' border of exon 2 was deduced by consideration of the potential splice donor sites in this region, only one prediced an ORF as a putative 1,2,4 product. Therefore, 5'-boundary of exon 2 shown in Figures 1A-1P is the only border that would encode a novel amino-terminal domain. Forward intron sequencing primers, 50-100 bp upstream of each exon, which were used to confirm these data [Table 3] . The TRAF-3 (p55) coding sequence is composed of 10 exons, which follow consensus splice donor and acceptor rules for exon/intron boundaries, and which were called 4 to 13. (See also Figures 1A-1P.)
Establishing intron size in TRAF-3 coding region
Determination of exon/intron boundaries allowed use of a PCR-based approach in order to determine intron size.
PCR was performed on both control human genomic DNA and on λ-phage and PI genomic clones. Oligonucleotide primer pairs spanning each of 9 consecutive coding exon/intron junctions were developed from the IHb cDNA sequence. These were used to amplify genomic human DNA.
The resulting PCR products, consisting of an intron bordered by two adjacent exon fragments, were sequenced to confirm their identity. The nine introns identified in this way ranged in size from 600 bp to 9.5 kb [Table 3] .
ALTERNATIVE SPLICING GENERATES DIFFERENT TRAF-3 ISOFORMS
A variety of EBV-transformed B cell lines were obtained from HIGM patients A, C, and B, and unaffected relatives of HIGM patients CM and DM. RT-PCR amplification of human TRAF-3 mRNA from these five donors revealed subtle length variations in cDNAs amplified from two regions of TRAF-3: the 5'-UTR and the zinc finger region. In all cases examined these length variations corresponded to the alternative splicing of specific TRAF-3 exons.
Alternative splicing of exon 3
Primers df7 and fr8, which span part of the 5'-UTR and the first 457 bp of the TRAF-3 coding sequence, were used to amplify cDNA from subjects A, B, C, and CM [Table 3] . These primers generated two TRAF-3 amplification products in approximately equal amounts.
The first was the 548 bp predicted from the published
TRAF-3 sequence. The second was a 687 bp fragment, which was detected in three of the four subjects studied
[B,A,CM] , and which was found to be identical to the smaller fragment except for the insertion of exon 3 in the 5'-UTR.
Zinc finger variants
External primers 3b210f and 3bl930r, which span the entire 1.9 kb TRAF-3 coding sequence, were used to amplify cDNA from subjects CM and DM. Sequencing of these variant amplification products revealed deletions Of 75 bp (IHb nt 875-949) , 156 bp (IHb nt 794-949) , and 168 bp (IHb nt 875-1042) in the zinc finger region. These deletions corresponded to the alternatively spliced loss of exons 9 (identified by Sato et al as CAP-1) ; loss of exons 8 and 9; and loss of exons 9 and 10. Such splicing is apparently uncommon, as the predominant isoform was the full length one, and only rare subclones contained the shorter, internally deleted messages.
DISCUSSION
Results of chromosomal FISH analysis and radiation hybrid screening in this study suggest that TRAF-3 is a single copy gene located on chromosome 14q32.2. This region plays a major role in B cell development as the immunoglobulin heavy chain switch region, which normally undergoes germline rearrangements during B cell development, and which is frequently involved in various translocations in certain hematologic diseases. It is therefore possible and even likely that the expression of TRAF-3 is regulated by the genomic splicing that takes place at this locus during normal B cell development, or is dysregulated by translocations. What the results of such events might be are difficult to predict. It may be for example, that normal rearrangements regulate expression of TRAF-3 by inactivating one allele, or that TRAF-3 is upregulated or, like bcr-abl , fused with other gene products during rearrangement or translocation.
Furthermore, the chromosomal localization of TRAF-3 may play a role in identifying that subset of HIGM patients who have a TRAF-3 defect. While the essential roles of CD40-L and CD40 in the phenotype of HIGM syndrome has been confirmed by targeted disruption of either CD40-L or CD40 in mice, no such evidence has yet been found for that subset of non-X-linked HIGM patients. Determination of defects in TRAF-3 may mediate immune deficiency syndromes with the HIGM phenotype. A subset of individuals with HIGM syndrome have normal CD40-L.
TRAF-3 may be linked with other genes that are associated with human diseases. In this regard, a form of HIGM with normal CD40-L was described that is associated with hypohidrotic ectoder al dysplasia, but in this family the syndrome appears to be inherited in an X-linked pattern and therefore may represent a different form of non-CD40-L HIGM. The chromosomal localization of TRAF-3 will be of interest, therefore, in identifying this and related syndromes.
Structural analysis reveals that TRAF-3 p55 is encoded by 10 exons (exons 4-13), which correspond roughly to protein domains predicted by the TRAF-3 cDNA sequence. Thus, exons 4 and 5 encode the zinc ring, exons 6-10 encode the zinc finger complex, exon 11 and the NH2- terminal encoding half of exon 12 encode the helical wheel, and the remaining half of 12 and 13 encode the N- TRAF domain and the TRAF-C domain is encoded by exon 13. Such structural detail is of general interest, as none of the TRAF family members have until now been analyzed at this level, and given their homology and similar functions, they presumably all have similar exonic arrangements. At the genomic level, for example, most of the structural complexity in TRAF-3 is seen in the zinc finger complex, a domain which appears to be regulated by alternative splicing. Interestingly, it has been noted that TRAF-2, which also has a multi-zinc finger domain, appears to undergo similar splicing.
The zinc finger complex consists of a single large exon, which encodes the 5' half of this region followed by three smaller exons, which encode the remaining zinc fingers. The organization described here suggests that the TRAF-3 zinc finger complex has evolved by the duplication of an original progenitor exon, leading to the addition of successive zinc fingers. Interestingly, a comparative amino acid analysis of TRAF-3 in the zinc finger complex shows that the in the 3' half of this domain there is 100% identity between murine and human sequences. By contrast, seven of the 80 preceding amino acids that make up the 5' half of this complex are divergent, and four of these seven changes are non- conservative. Such conservation in the 3' part of this complex implies that this portion of the zinc finger complex is significant in the signaling function of TRAF-3.
A total of three unique mRNAs which vary in this region have been isolated, the deletion of exon 9, deletion of exons 8 and 9, and deletion of exons 9 and 10 as TRAF-3 isoforms. Each of these variants is in frame, and each deletion corresponds to the loss of one or two adjacent exons in this region. Therefore, each isoform encodes a different combination of zinc fingers in the 3' half of this complex. This interchangability of exons is made possible by their common coding class, which ensures that removal or insertion of a given exon will not affect reading frame [Table 3] . The possible consequences of such splicing are intriguing, in that zinc fingers commonly mediate both protein-protein and protein-DNA interactions. Each of these isoforms may interact with separate constituents of the cytoplasmic signaling apparatus, for example. Such variation in a highly conserved and presumably important functional portion of this protein, therefore, implies a potential regulation by alternative splicing of TRAF-3's role as a signaling molecule.
Evidence for the alternative use of exons has not been limited to the TRAF-3 coding sequence, but was initially revealed in the 5'-UTR, through variation among cDNA clones in exons 2, 3, and 4-13. The significance of this phenomenon (which is quite common, at least with respect to exon 3) , is uncertain. It should be noted, however, that the IHb form of TRAF-3 contains an open reading frame which precedes the initiating methionine at IHb nt positio 224. Interestingly, exon 2 is in frame with the rest of TRAF-3. Thus, while the inclusion of exon 3 leads to an early stop in translation, its removal allows for the production of a longer TRAF-3 species, exons 1,2,4-13.
It is not immediately clear how the described genomic structure of CRAFl encodes p55, since in standard cell biology, a transcript including both exon 1 and 3 would terminate translation in the region of cDNA of exon 3 that contains a stop codon. However, p55 could be encoded by the gene described herein, due to alternative promoters, alternative transcription initiation, alternative translation initiation or internal ribosomal re-entry.
Alternative promoters (e.g., c-able gene (Bernards, A., et al . 1988. Oncogene 2:297)) could be present if an undetected promoter exists in the 1-2 intron (such a promoter may be a "TATA-less" promoter (Smale, S. T. and
D. Baltimore. 1989. Cell 57:103) in this G-C rich region
(e.g., Bloom syndrome gene (Ellis, N. A., et al. 1995.
Cell S3:655) and if this transcript initiated after the AUG that encodes p70. Another possibility is that an alternative promoter exists in the 2-3 intron (encoding a cDNA encoded by exons 3-13 and encoding the p55 isoforms) (e.g. , CD23 gene (Yokota, A., et al. 1988. Cell 55:611) . Whether or not an alternative promoter exists, p55 encoding transcripts could arise by alternative transcription initiation sites (Hall, L. R. , et al . 1988. J. Immunol . 141:2781) , which possibility is favored by the lack of strong transcription initiation sites in the putative 5'-UT of exon 1, such as the TATA box and the CCAAT box (Bucher, P. and E. N. Trifonov. 1988. J of Biomolecular Structure & Dynamics 5:1231; Bucher, P. and E. N. Trifonov. 1986. NAR 14:10009) identified in Figures 10A-10D. (e.g. as in CD45 gene) . Alternative translation initiation sites have also been shown to exist in certain cases and could lead to the generation of the p55 peptide species. Another possibility is that an internal ribosomal re-initiation sites might exist, in the cDNA and lead to p55 peptide species by cap-independent translation (Jang, S. K. , et al. 1988. J. Virol . 62 : 2636 ; Molla, A., et al. 1992. Nature 356:255; Pelletier, J. and N. Sonenberg. 1988. Nature 334:320. It should be noted that one or more of these strategies could be combined with alternative splicing to yield TRAF-3 isoforms that initiate translation in mRNA encoded by exon 10, (Mosialos, G. , et al. 1995. Cel l 80 : 389 ) .
If this is the case than there may be two initiation sites for TRAF-3. A second, and unrelated possibility is that such alternative exons, like alternative poly- adenylation at the 3' terminus of many mRNAs, may have some processing or regulatory significance, for example, by influencing message stability.
These various isoforms may play a role in modulating signaling mediated by TRAF-3. Each isoform, for example, may participate in a different signaling pathway, and may have a different level of expression or activity in a given cell. Some forms may act to inhibit others, or may be present only at critical moments in cellular development. The over-expression of these isoforms, therefore, in various cell lines may reveal important functional differences between them.
METHODS
Human metaphase spreads were prepared from fibroblast line. Ramos clone 2G6.4CN 3F10. Chromosome 14 telomere probe was purchased from Oncor.
A λ-gtll Raji cDNA library (Stratagene) was screened. Probed with a 5' probe: Notl-SacI and with a 3' probe: C26. Clones were isolated by plating phage according to standard procedures on lawns of E. coli and plaque purified.
A human genomic λ-fix library (Stratagene) was screened. Clones were isolated by plating phage according to standard procedures on lawns of E. coli (P2932) and plaque purified. A human genomic 3.5x arrayed PI artificial chromosome library was used. Average insert size is 100 kb. This was prepared by partial Sau3AI digest and ligated into PCYPAC2. The library was screened with CRAFl specific probes. Clones were isolated by transforming E. coli (DH10B) , printing colonies (6144 colonies/filter) onto high density nylon membranes (SureBlot, Oncor) using the Biomek 2000 Automated Laboratory Workstation equipped with a high density replicating system (Beckman) , and processing filters as described by Olsen et al .
(BioTechniques 14:116-23 (1993)) . Probes were labeled using random primers and filters were hybridized according to standard conditions (Genomics 21:525-37
(1994) ) .
The following probes were used to screen cDNA and genomic libraries as well as Southern blots: IHb (IHb 1-2467) a 2.4 kb cDNA which contains exon 2 as well as the entire TRAF-3 open reading frame. Notl-S al (IHb nt 26-128) , a 102 bp restriction fragment which contains the 5' half of exon 2. NotI-Sad, a probe which represents the first 447 bp of IHb. CE (lb nt 12-205) , a 193 bp probe derived from cDNA clone lb which represents a part of the TRAF-3 5'-UTR and contains exon E. Hindi-Hindi (IHb 606-1003) . zfl (2-1 nt 158-82)
(tggcaaactggctaccctgtccacc Seq I.D. No. ) is a carboxy-terminal oligonucleotide fragment of exon 1. ff7gen-fr8gen is a 4.1 kb genomic fragment generated by genomic PCR using primers ff7gen and frβgen (Table 3) which spans exons 5 and 6. pstlc-r2glx is a 5.8 kb genomic fragment generated by genomic PCR using primers pstlc and r2glx which spans exons 8 to 10.
λ phage genomic clones were sequenced on an automated DNA sequencer (ABI) using 5.0 μg per sequencing reaction. PI clones were sequenced manually by cycle sequencing (Gibco Cycle Sequencing kit) using 1.5 μg template DNA under the following conditions: DNA initial denaturation 95 °C 3 min; denaturation 95 °C 30 sec, annealing 64 °C 30 sec, extension 70 °C 60 sec X 20 cycles; denaturation 95 °C 30 sec, extension 70 °C 60 sec X 15 cycles.
Genomic PCR was carried out using the Expand long template PCR kit (Boehringer-Mannheim) as per the manufacturers directions. Human genomic DNA was extracted from Ramos cells as follows: 50 x 106 cells pelleted lx and washed 2x in PBS 5 min at 500 G, resuspended in 0.5 ml digestion buffer (100 mM NaCl, 10 mM TrisCl pH 8.0, 25 mM EDTA pH 8.0, 0.5% SDS, 0.1 mg/ml proteinase K) , incubated with gentle shaking at 50 °C 18 hrs, phenol-chloroform extracted 3x, and dialyzed against TE 24 hrs (Current Protocols 2.2, Ausubel et al . 1992) . The following PCR conditions were used: initial denaturation 94 °C 4 min x 1 cycle; denaturation 94 °C 30 sec, annealing 62 °C 30 sec, extension 68 °C 15 min x 10 cycles; denaturation 94 °C 30 sec, annealing 62 °C
30 sec, extension 68 °C 15 min with 20 sec additional extension per cycle x 30 cycles; final extension 68 °C
7 min. Genomic PCR products were gel purified
(Qiaquick) , subcloned (except 7-8, which was sequenced directly) into pCR 2.0 or 2.1 (Invitrogen), and sequenced on an automated DNA sequencer (ABI) at the Columbia Sequencing Center, using standard conditions (0.5 μg per sequencing reaction) .
RT-PCR of the zinc-finger complex and the 5'-UTR regions were performed as follows. HIGM patients A and C, and C's unaffected mother CM were used. Patient B and an unaffected mother of another HIGM patient, RS, were provided. Total RNA was extracted (RNeasy kit: Qiagen) from EBV-immortalized human B cell lines from all five donors. RNA was oligo-dT primed and reverse transcribed into cDNA (Superscript II, Gibco BRL) . cDNA was amplified by PCR in the 5'-UTR using primers df7 (IHb nt 133-150) agcagaacgctgcggacc (Seq. I.D. No. ) and frδ (IHb nt 681-664) cagtcaggacgcacacat (Seq. I.D.
No. ) , and in the zinc finger complex using primers 3b210f (IHb nt 209-227) ctcctctttcctaaaatgg
(Seq. I.D. No. ) and 3bl930r (IHb nt 1949-1921) agctacttatcagggatcg (Seq. I.D. No. ) . All RT-PCR products were separated by agarose gel electrophoresis and visualized by staining with ethidium bromide. RT- PCR products were gel purified and ligated into pCR2.0 and 2.1 (Invitrogen) . Ligation products were cloned in E. coli and clones were examined for insert.
Further Comments on CRAFl peptide and CRAFl peptide isoforms
Despite wide tissue distribution CRAFl peptide appears to have distinct and essential role in contact-help. CD40 is broadly expressed in many types of cells. CRAFl peptide is ubiquitously expressed. Targeted gene disruption of CRAFl nucleic acid results in defective contact-dependent helper function. Despite "collateral" signaling pathways, CRAFl peptide is essential for T helper function. Analysis of CRAFl nucleic acid mRNA revealed alternative mRNA splicing. A variety of CRAFl nucleic acid mRNA species were isolated. A variety of splicing events alters the number of zinc-finger like domains. The three CRAFl peptide isoforms are predicted by cDNA encoding loss of Zn-finger encoding exons. What is the evidence that longer CRAFl nucleic acid mRNA species is important in regulating CD40 signaling? The IHb type species (with an appended amino terminal peptide domain) is expressed by activated B cells and fibroblasts by RT-PCR. Hyper IgM patients with normal CD40-L preferentially express p70. Two unrelated HIGM patients expressed abnormal ratio of p70 and p60 mRNA. HIGM patients may overexpress p70 encoding mRNA. They may lack an in fram stop codon in exon 3. Therapeutics
CRAFl peptide and variants thereof and isoforms thereof combined with carriers or therapeutically acceptable agents for delivery may be used as therapeutic compositions or therapeutic pharmaceuticals for administration to subjects. Dominant negative CRAFl peptide may be used in gene therapy as immunomodulator or i munosuppressive therapeutics. Such peptides may be co-administered with other therapeutic genes. Peptide minmetics or small molecules are examples of agents which may be used to mimic inhibitory CRAFl peptides. Screening would be facilitated by identification of p70 interacting species by systems such as the two-hybrid yeast system.
Genomic sequencing has been done using the genomic clones as described in Figures 7A-7B, 8 and 9A-9C.
Table 3. Genomic PCR and sequencing primers
Figure imgf000104_0001
Table 3 continued
Figure imgf000105_0001
Numbering is based on clone Illb which is deposited in the GenomeBank.
Figure imgf000106_0001
REFERENCES
References for Background
1. S. Paulie et al. , Cancer Immunol. Immunother. 20, 23(1985) ; E.A. Clark and J.A. Ledbetter, Proc. Natl. Acad. Sci. U.S.A. 83, 4494 (1986) ; I.
Stamenkovic, E.A. Clark, B. Seed, EMBO J. 8, 1403 (1989) .
2. S. Lederman et al. , J. Exp. Med. 175, 1091 (1992) ; R. J. Armitage et al. , Nature 357, 80(1992) ; D. Graf, U. Korthauer, H.W. Mages, G. Senger, R.A.
Kroczek, Eur. J. Immunol. 22, 3191 (1992) ; J.F. Gauchat et al. , FEBS Lett. 315, 259 (1993) .
3. S. Lederman et al. , J. Immunol. 149, 3817 (1992) .
4. D. Hollenbaugh et al. , EMBO J. 11, 4313 (1992) . 5. T. Tsukata, J. Wu, T. Honjo, Nature 364, 645 (1993) ; N.J. Holder et al . , Eur. J. Immunol. 23, 2368 (1993) ; S.L. Parry, J. Hasbold, M. Holman, G.G.B. Klaus J. Immunol. 152, 2821 (1994) . 6. M.J. Yellin et al . , J. Immunol. 153, 666 (1994) . 7. R.C. Allen et al . , Science 259, 990 (1993) ; U. Korthauer et al. , Nature 361, 539 (1993) ; J.P. DiSanto et al. , ibid., p.541; A. Aruffo et al . , Cell 72, 291 (1993) ; R.E. Callard et al. , J. Immunol. 153, 3295 (1994) ; N. Ramesh et al . , Int. Immunol. 5, 769 (1993) .
8. J. Xu et al., Immunity 1, 423 (1994) .
9. T. Kawabe et al. , ibid., p. 167.
10. F. Schrieve et al., J. Exp. Med. 169, 2043 (1989) ; E.A. Clark, K.H. Grabstein, G.L. Shu, J. Immunol. 148, 3327 (1992) .
11. D.N. Hart and J.L. McKenzie, J. Exp. Med. 168, 157
(1988) .
12. M.R. Alderson et al . , ibid. 178, 669 (1993) .
13. A.H. Galy and H. Spits, J. Immunol. 149, 775 (1992) .
14. F.H. Durie, T.M. Foy, S.R. Masters, J.D. Laman, R.J. Noelle, Immunol. Today 15, 406 (1994) . 15. S. Inui et al . , Eur. J. Immunol. 20, 1747 (1990) .
References for Detailed Description and Example 1 of Experimental Details 1. Lederman, S., et al . 1992. J. Exp. Med. 175:1091.
2. Armitage, R. J., et al . 1992. Nature 357:80.
3. Lederman, S., et al . 1992. J". Immunol. 149:3817.
4. Graf, D., et al . 1992. Eur. J". Immunol. 22:3191.
5. Hollenbaugh, D. , et al . 1992. EMBO J. 11:4313. 6. Spriggs, M. K. , et al. 1992. J. Exp. Med. 176:1543.
7. Lane, P., et al. 1992. Eur. J. Immunol. 22:2573.
8. Hermann, P., et al. 1993. Eur. J. Immunol. 23:961.
9. Gauchat, J. F., et al . 1993. FEBS Lett. 315:259.
10. Covey, L. R., et al . 1994. Mol . Immunol. 31:471. 11. Lederman, S. ,et al . 1994. J. Immunol. 152:2163.
12. Rosen, F. S., et al.1961. Pediatrics 28:182.
13. Mayer, L. , et al.1986.. N. Engl . J. Med. 314:409.
14. Notarangelo, L. D., et al.1992. Immunodefic. Rev. 3:101. 15. Fuleihan, R. , et al. 1993. Proc. Natl. Acad. Sci. U. S. A. 90:2170.
16. Korthauer, U., et al.1993. Nature 361:539.
17. DiSanto, J. P., et al. 1993. Nature 361:541.
18. Allen, R. C, et al. 1993. Science 259:990. 19. Aruffo, A., et al . 1993. Cell 72:291.
20. Facchetti, F., et al . 1995. J. Immunol. 154:6624.
21. Ramesh, N. , et al. 1993. Int. Immunol. 5:769.
22. Callard, R. E., et al.1994. J. Immunol. 153:3295.
23. Xu, J., et al. 1994. Immunity 1:423. 24. Renshaw, B. R. , et al. 1994. Journal of Experimental Medicine 180:1889.
25. Kawabe, T., et al.1994. Immunity 1:167.
26. Castigli, E., et al. 1994. PNAS USA 91:12135.
27. Noelle, R. J., et al . 1992. Proc. Natl. Acad. Sci. U. S. A. 89:6550.
28. Van den Eertwegh, A. J. M., et al . 1993. J. Exp. Med. 178:1555. 29. Foy, T. M. et al. 1993. J. Exp. Med. 178:1567.
31. Clark, E. A. and J. A. Ledbetter. 1994. Nature 367:425.
32. Noelle, R. J. and E. C. Snow. 1990. Immunol. Today 11:361.
33. Springer, T. A. 1990. Nature 346:425.
34. Lederman, S. and L. Chess. 1987. Ann. Inst. Pasteur Immunol. 138:158.
35. Lederman, S et al . 1993. Curr. Opin. Immunol. 5:439.
36. Klaus, S. J. et al 1994. J. Immunol. 152:5643.
37. Valentine, M A. and K. A. Licciardi. 1992. Eur. J. Immunol. 22:3141.
38. Liu, Y. J., et al 1989. Nature 342:929. 39. Liu, Y. J., et al . 1991. Eur. J. Immunol. 21:1905.
40. Tsubata, T., et al 1993. Nature 364:645.
41. Holder, M. J. , et al . 1993. Eur. J". Immunol. 23:2368.
42. Casamayor-Palleja, C, et al.1995. J. Exp. Med. 151:1293.
43. Stamenkovic, I., et al. 1989. EMBO J. 8:1403.
44. Smith, C. A., et al . 1994. Cell 76:959.
45. Browning, J. L. , et al . 1993. Cell 72:847.
46. Suda, T., et al . 1993. Cell 75:1169. 47. Goodwin, R. G. , et al . 1993. Cell 73:447.
48. Bowman, M. R., et al . 1994. J. Immunol. 152:1156.
49. Hintzen, R. Q., et al. 1994. J. Immunol. 152:1162.
50. Smith, C. A., et al. 1993. Cell 73:1349.
51. Goodwin, R. G., et al. 1993. Eur. J". Immunol . 23:2631.
52. Tartaglia, L. A. and D. V. Goeddel . 1992 Immunol . Today 13:151.
53. Trauth, B. C, et al . 1989. Science 245:301.
54. Itoh, Ν., et al 1991. Cell 66:233. 5 555. Camerini, D., et al . 1991. J". Immunol. 147:3165. 56 Pollok, K. E., et al . 1993. J. Immunol. 150:111. 57 Crowe, P. D., et al . 1994. Science 264:101. 58. Mallett, S. , et al . 1990. EMBO J. 9:1063.
59. De Togni, P., et al. 1994. Science 264:103.
60. Jelinek, D. F. and P. E. Lipsky. 1987. J. Immunol. 139:2910. 61. Boussiotis, V. A., et al . 1994. PNAS USA 91:1001.
62. Aversa, G., et al . 1993. J. Exp. Med. 177:1575.
63. Macchia, D., et al . 1993. Nature 36"3:464.
64. Watanabe Fukunaga, R., et al. 1992. Nature 356:314.
65. Chu, J. L., et al . 1993. J. Exp. Med. 178:123. 66. Adachi, M. , et al 1993. Proc. Natl. Acad. Sci. U. S. A. 90:1156.
67. Rieux-Laucat, F., et al . 1995. Science 268:1341.
68. Cohen, P. L. and R. A. Eisenberg. 1991. Annu. Rev. Immunol. 9P243-69.243. 69. Reap, E. A., et al . 1995. J of Immun 154:936.
70. Dhein, J., et al . 1995. Nature 373:438.
71. Brunner, T., et al . 1995. Nature 373:441.
72. Ju, S. T., et al. 1993 Nature 373:444.
73. Liu, Y., et al. 1992. Immunol. Today 13:11. 74. Conley, M. E., et al . 1994. J. Clin. Invest. 94:1404.
75. Cheng, G., et al . 1995. Science 267:1494.
76. Yellin, M. J., et al . 1991. J. Immunol. 147:3389. 11. Rothe, M., et al . 1994. Cell 78:681. 78. Grabstein, K. H. , et al . 1993. J. Immunol. 150:tl)3141.
79. Lane, P., et al. 1993. J. Exp. Med. 177:1209.
80. Maliszewski. C. R., et al . 1993. Eur. J. Immunol. 23:1044. 81. Armitage, R. J. , et al. 1993. J. Immunol. 150:3611.
82. Durandy, A., et al . 1993. Eur. J. Immunol. 23:2294.
83. Jung, S., et al . 1993. Science 259:984.
84. Gascan, H., et al. 1991. J. Exp. Med. 173:141.
85. Gauchat, J. F., et al . 1992. J. Immunol. 148:2291. 86. Schultz, C. L., et al. 1992. J. Immunol. 149:60.
87. Jumper, M. D., et al. 1994. J. Immunol. 152:438.
88. Yellin, M. J., et al . 1994. J. Immunol. 153:666. 89. Linsley, P. S., et al . 1992. Science 257:792.
90. Ranheim, E. A. and T. J. Kipps. 1993. J. Exp. Med. 177:925.
91. Fluckiger, A. C, et al . 1992. Blood 80:3113. 92. Yellin, M. J., et al. 1994. J. Immunol. 152:598.
93. Ktistakis, N. T., et al . 1990. J. Cell Biol. 111:1393.
95. Lagresle, C. , et al . 1995. Eur. J. Immunol. 154:5146. 96. Inui, S., et al . 1990. Eur. J. Immunol. 20:1141.
97. Siegel, J. P. and H. S. Mostowski. 1990. J. Immunol. Methods 132:281.
98. Mosialos, G., et al. 1995. Cell 80:389. (Abstract)
99. Hu, H. M., et al . 1994. J Biol Chem 269:30069. 100. Hsu, H., et al . 1995. Cell 81:495.
101. Stanger, B. Z., et al . 1995. Cell 81:513.
102. Chinnaiyan, A. M., et al. 1995. Cell 81:505.
103. Clark, E. A., et al . 1989. J. Immunol. 143:3813.
104. Splawski, J. B. and P. E. Lipsky. 1994. Research in Immunology 145:226.
105. Banchereau, J. and F. Rousset. 1991. Nature 353:678.
106. Clark, E. A., et al. 1988. Eur. J. Immunol. 18:451.
107. Barrett, T. B., et al . 1991. J. Immunol. 146:1122. 108. Koopman, G. , et al . 1994. J. Immunol. 152:3160.
109. Sumimoto, S., et al . 1994. Journal of Immunology 153:2488.
110. Henderson, S., et al. 1991. Cell 65:1101.
111. Wang, F., et al. 1990. J". Virol. 54:2309. 112. Zhang, Q., et al. 1994. European Journal of Immunology 24:1461.
113. Martin, J. M. , et al . 1993. Journal of Virology 67:5269.
114. Tewari, M. and V. M. Dixit . 1995. J. Biol. Chem. 270:3255.
115. Tewari, M. , et al . 1995. Cell 81:801.
116. Gulbins, E., et al . 1995. Immunity 2:341. 117. Wang, X., et al. 1994. Cell 77:53.
118. Darnell, J. E., Jr., et al . 1994. Science 264:1415.
References for Example 2 ; 1. Lederman, S., et al. 1992. J. Exp. Med. 175:1091.
2. Armitage, R. J., et al. 1992. Nature 357:80.
3. Lederman, S., et al. 1992. J". Immunol. 149:3811.
4. Graf, D., et al. 1992. Eur. J. Immunol. 22:3191.
5. Hollenbaugh, D., et al. 1992. EMBO J. 11:4313. 6. Spriggs, M. K., et al. 1992. J. Exp. Med. 176:1543.
1. Lane, P., et al. 1992. Eur. J. Immunol. 22:2573.
8. Hermann, P., et al. 1993. Eur. J. Immunol. 23:961.
9. Gauchat, J. F., et al. 1993. FEBS Lett. 315:259.
10. Covey, L. R., et al.1994. Mol . Immunol. 31:411. 11. Rosen, F. S., et al. 1961. Pediatrics 28:182.
12. Mayer, L., et al. 1986. N. Engl. J. Med. 314:409.
13. Νotarangelo, L. D.,et al.1992. Immunodefic. Rev. 3:101.
14. Fuleihan, R.,et al. 1993. Proc. Natl. Acad. Sci. U. S. A. 90:2110.
15. Korthauer, U., et al. 1993. Nature 361:539.
16. DiSanto, J. P., et al. 1993. Nature 36-1:541.
17. Allen, R. C, et al. 1993. Science 259:990.
18. Aruffo, A., M. et al. 1993. Cell 72:291. 19. Facchetti, F., C. et al. 1995. J. Immunol. 154:6624.
20. Ramesh, Ν. , R. et al. 1993. Int. Immunol. 5:169.
21. Callard, R. E., et al. 1994. J". Immunol. 153:3295.
22. Kawabe, T., et al. 1994. Immunity 1:167.
23. Castigli, E., et al. 1994. Proc Natl Acad Sci USA 91:12135.
24. Xu, J., et al. 1994. Immunity 1:423.
25. Renshaw, B. R. et al. 1994. J Exp Med 180:1889.
26. Cheng, G., et al. 1995. Science 267:1494.
27. Mosialos, G., et al. 1995. Cell 80:389. 28. Hu, H. M., et al. 1994. J Biol Chem 269:30069.
29. Sato, T., S. Irie, and J. C. Reed. 1995. FEBS Letters 358:113. - Ill -
30. Lederman, S., et al. 1994. J. Immunol. 152:2163.
31. Inui, S., et al. 1990. Eur. J. Immunol. 20:1141.
32. Valentine, M. A. and K. A. Licciardi. 1992. Eur. J. Immunol. 22:3141. 33. Liu, Y. J., et al. 1989. Nature 342:929.
34. Liu, Y. J., et al. 1991. Eur. J". Immunol. 21:1905.
35. Tsubata, T., et al. 1993. Nature 364:645.
36. Holder, M. J., et al. 1993. Eur. J. Immunol. 23:2368. 37. Conley, M. E., et al. 1994. J". Clin. Invest. 94:1404.
38. Rieux-Laucat, F.,et al. 1995. Science 268:1341.
39. Durandy, A.,et al. 1993. Eur. J". Immunol. 23:2294.
40. Ranheim, E. A. and T. J. Kipps. 1993.J". Exp. Med. 177:925.
41. Rothe, M., et al. 1994. Cell 78:681.
42. Wang, X., et al. 1994. Cell 77:53.
43. Darnell, J. E., et al.1994. Science 264:1415.
44. Zhang, J., et al. 1994. Oncogene 9:1931. 45. Νeri, A.,et al. 1991. Cell 67:1015.
46. Chang, C. C.,et al. 1994. Oncogene 9:923.
47. Cuomo, L., et al. 1993. International Journal of Cancer 53:1008.
48. Coney, L. R., et al. 1994. International Journal of Cancer 58:562.
49. Siegel, J. P. and H. S. Mostowski. 1990. J. Immunol. Methods 132:281.
50. Littman, D. R., et al. 1985. Cell 40:231.
51. Koopman, G., et al. 1994. J. Immunol. 152:3160. 52. Wyllie, A. H. , et al.1980. Cytol . 68:251.
53. Benhamou, L. E., et al. 1990. Eur. J. Immunol. 20:1405.

Claims

What is claimed is:
1. An isolated protein comprising a CRAFl-b domain which comprises GGARRGRRVREPGLQPSRDFPAGGSRGGRRLFPAPRHGAARGAERCGPRRT
RPAPLSRPSGDGPRELLFPKM or a variant thereof capable of inhibiting CD40-mediated cell activation.
2. The protein of claim 1, further comprising CRAFl-a or a variant thereof adjacent to the carboxy- terminus of the CRAFl-b domain.
3. The protein of claim 1, wherein the CRAFl-b domain comprises at least 72 amino acids.
4. The protein of claim 1, wherein the CRAFl-b domain comprises about 150 amino acids.
5. The protein of claim 1, wherein the variant comprises a conservative amino acid substitution.
6. A CRAFl peptide.
7. The peptide of claim 6, wherein the peptide comprises an amino acid sequence encoded by exon X.
8. The peptide of claim 6, wherein the peptide comprises an amino acid sequence encoded by exon Y.
9. A method of inhibiting activation by CD40 ligand of cells expressing CD40 on the cell surface, comprising providing the cells with the protein of claim 1 or 6, the protein being present in an amount effective to inhibit activation of the cells.
10. The method of claim 9, wherein the cells are provided with the protein by introducing into the cells a nucleic acid sequence encoding the protein under conditions such that the cells express an amount of the protein effective to inhibit activation of the cells.
11. The method of claim 10, wherein the nucleic acid sequence is operably linked to a transcriptional control sequence recognized by the cell.
12. The method of claim 10, wherein the nucleic acid sequence is a plasmid.
13. The method of claim 9, wherein the CD40-bearing cells are selected from the group consisting of B cells, fibroblasts, endothelial cells, epithelial cells, T cells, basophils, macrophages, Reed- Steinberg cells, dendritic cells, renal cells, and smooth muscle cells.
14. The method of claim 13, wherein the B cells are resting B cells, primed B cells, myeloma cells, lymphocytic leukemia B cells, or B lymphoma cells.
15. The method of claim 9, wherein the epithelial cells are keratinocytes.
16. The method of claim 9, wherein the fibroblasts are synovial membrane fibroblasts, dermal fibroblasts, pulmonary fibroblasts, or liver fibroblasts.
17. The method of claim 9, wherein the renal cells are selected from the group consisting of glomerular endothelial cells, mesangial cells, distal tubule cells, proximal tubule cells, parietal epithelial cells, visceral epithelial cells, cells of a Henle limb, and interstitial inflammatory cells. 18. The method of claim 17, wherein the parietal epithelial cells are crescent parietal epithelial cells.
19. The method of claim 9, wherein the smooth muscle cells are smooth muscle cells of the bladder, vascular smooth muscle cells, aortic smooth muscle cells, coronary smooth muscle cells, pulmonary smooth muscle cells, or gastrointestinal smooth muscle cells.
20. The method of claim 19, wherein the gastrointestinal smooth muscle cells are esophageal smooth muscle cells, stomachic smooth muscle cells, smooth muscle cells of the small intestine, or smooth muscle cells of the large intestine.
21. A method of providing a subject with an amount of the protein of claim 1 or 6 effective to inhibit activation by CD40 ligand of cells bearing CD40 on the cell surface in the subject, comprising: introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein of claim 1 or 6, under conditions such that the cells express in the subject an activation inhibiting effective amount of the protein.
22. The method of claim 21, wherein the introducing of the nucleic acid into cells of the subject comprises : a) treating cells of the subject ex vivo to insert the nucleic acid sequence into the cells; and b) introducing the cells from step a) into the subject. 23. The method of claim 21, wherein the subject is a mammal .
24. The method of claim 23, wherein the mammalian subject is a human.
25. The method of claim 21, wherein the CD40-bearing cells are selected from the group consisting of B cells, fibroblasts, endothelial cells, epithelial cells, T cells, basophils, macrophages, Reed-
Steinberg cells, dendritic cells, renal cells, and smooth muscle cells.
26. The method of claim 25, wherein the B cells are resting B cells, primed B cells, myeloma cells, lymphocytic leukemia B cells, or B lymphoma cells.
27. The method of claim 25, wherein the epithelial cells are keratinocytes.
28. The method of claim 25, wherein the fibroblasts are synovial membrane fibroblasts, dermal fibroblasts, pulmonary fibroblasts, or liver fibroblasts.
29. The method of claim 25, wherein the renal cells are selected from the group consisting of glomerular endothelial cells, mesangial cells, distal tubule cells, proximal tubule cells, parietal epithelial cells, visceral epithelial cells, cells of a Henle limb, and interstitial inflammatory cells.
30. The method of claim 29, wherein the parietal epithelial cells are crescent parietal epithelial cells.
31. The method of claim 25, wherein the smooth muscle cells are smooth muscle cells of the bladder, vascular smooth muscle cells, aortic smooth muscle cells, coronary smooth muscle cells, pulmonary smooth muscle cells, or gastrointestinal smooth muscle cells.
32. The method of claim 31, wherein the gastrointestinal smooth muscle cells are esophageal smooth muscle cells, stomachic smooth muscle cells, smooth muscle cells of the small intestine, or smooth muscle cells of the large intestine.
33. A method of treating a condition characterized by an aberrant or unwanted level of CD40-mediated intracellular signaling, in a subject, comprising providing the subject with a therapeutically effective amount of the protein of claim 1 or 6 capable of inhibiting CD40-mediated intracellular signaling in cells bearing CD40 on the cell surface.
34. The method of claim 33, wherein the protein is provided by introducing into CD40-bearing cells of the subject, a nucleic acid sequence encoding the protein under conditions such that the cells express the protein according to the method of claim 21.
35. The method of claim 33, wherein the condition is organ rejection in a subject receiving transplant organs, or an immune response in a subject receiving gene therapy.
36. The method of claim 35, wherein the transplant organ is a kidney, heart or liver.
37. The method of claim 35, wherein the condition is a CD40-dependent immune response. 38. The method of claim 37, wherein the CD40-dependent immune response is an autoimmune response in a subject suffering from an autoimmune disease.
39. The method of claim 38, wherein the autoimmune disease comprises rheumatoid arthritis, Myasthenia gravis, systemic lupus erythematosus, Graves' disease, idiopathic thrombocytopenia purpura, hemolytic anemia, diabetes mellitus, a drug-induced autoimmune disease, psoriasis, or hyper IgE syndrome.
40. The method of claim 39, wherein the drug-induced autoimmune disease is drug-induced lupus.
41. The method of claim 39, wherein the immune response comprises induction of CD23, CD80 upregulation, rescue from CD95-mediated apoptosis, rescue from apoptosis in a subject undergoing chemotherapy against a tumor, or autoimmune manifestations of an infectious disease.
42. The method of claim 41, wherein the autoimmune manifestations are derived from Reiter's syndrome, spondyloarthritis, Lyme disease, HIV infections, syphilis or tuberculosis.
43. The method of claim 34, wherein the condition is an allergic response.
45. A method of claim 44, wherein the allergic response is hay fever or a penicillin allergy.
46. The method of claim 35, wherein the condition is dependent on CD40 ligand-induced activation of fibroblast cells. 47. The method of claim 46, wherein the condition is selected from the group consisting of arthritis, scleroderma, and fibrosis.
48. The method of claim 47, wherein the arthritis is rheumatoid arthritis, non-rheumatoid inflammatory arthritis, arthritis associated with Lyme disease, or osteoarthritis.
49. The method of claim 47, wherein the fibrosis is pulmonary fibrosis, hypersensitivity pulmonary fibrosis, or a pneumoconiosis.
50. The method of claim 49, wherein the pulmonary fibrosis is pulmonary fibrosis secondary to adult respiratory distress syndrome, drug-induced pulmonary fibrosis, idiopathic pulmonary fibrosis, or hypersensitivity pneumonitis.
51. The method of claim 49, wherein the pneumoconiosis is asbestosis, siliconosis, or Farmer's lung.
52. The method of claim 43, wherein the fibrosis is a fibrotic disease of the liver or lung.
53. The method of claim 52, wherein the fibrotic disease of the lung is caused by rheumatoid arthritis or scleroderma.
54. The method of claim 52, wherein the fibrotic disease of the liver is selected from the group consisting of :
Hepatitis-C; Hepatitis-B; cirrhosis; cirrhosis of the liver secondary to a toxic insult; cirrhosis of the liver secondary to drugs; cirrhosis of the liver secondary to a viral infection; and cirrhosis of the liver secondary to an autoimmune disease.
55. The method of claim 54, wherein the toxic insult is alcohol consumption.
56. The method of claim 54, wherein the viral infection is Hepatitis B, Hepatitis C, or hepatitis non-B non-C.
57. The method of claim 54, wherein the autoimmune disease is primary biliary cirrhosis, or Lupoid hepatitis.
58. The method of claim 34, wherein the condition is dependent on CD40 ligand-induced activation of endothelial cells.
59. The method of claim 58, wherein the condition is selected from the group consisting of atherosclerosis, reperfusion injury, allograft rejection, organ rejection, and chronic inflammatory autoimmune diseases.
60. The method of claim 59, wherein the atherosclerosis is accelerated atherosclerosis associated with organ transplantation.
61. The method of claim 59, wherein the chronic inflammatory autoimmune disease is vasculitis, rheumatoid arthritis, scleroderma, or multiple sclerosis.
62. The method of claim 34, wherein the condition is dependent on CD40 ligand-induced activation of epithelial cells.
63. The method of claim 62 wherein the epithelial cells are keratinocytes, and the condition is psoriasis.
64. The method of claim 34, wherein the condition is an inflammatory kidney disease.
65. The method of claim 64, wherein the inflammatory kidney disease is not initiated by autoantibody deposition in kidney.
66. The method of claim 64, wherein the kidney disease is selected from the group consisting of: membranous glomerulonephritis; minimal change disease/acute tubular necrosis; pauci-immune glomerulonephritis; focal segmental glomerulosclerosis; interstitial nephritis; antitissue antibody-induced glomerular injury; circulating immune-complex disease; a glomerulopathy associated with a multisystem disease; and drug-induced glomerular disease.
67. The method of claim 66, wherein the antitissue antibody-induced glomerular injury is anti-basement membrane antibody disease.
68. The method of claim 66, wherein the circulating immune-complex disease is selected from the group consisting of: infective endocarditis; leprosy; syphilis; hepatitis B; malaria; and a disease associated with an endogenous antigen.
69. The method of claim 68, wherein the endogenous antigen is DNA, thyroglobulin, an autologous immunoglobulin, erythrocyte stroma, a renal tubule antigen, a tumor-specific antigen, or a tumor- associated antigen.
70. The method of claim 66 wherein the glomerulopathy associated with a multisystem disease is selected from the group consisting of : diabetic nephropathy; systemic lupus erythematosus;
Goodpasture's disease; Henoch-Schόnlein purpura; polyarteritis; Wegener's granulomatosis; cryoimmunoglobulinemia; multiple myeloma;
Waldenstrδm's macroglobulinemia; and amyloidosis.
71. The method of claim 66, wherein the pauci-immune glomerulonephritis is ANCA+ pauci-immune glomerulonephritis, or Wegener's granulomatosis.
72. The method of claim 66, wherein the interstitial nephritis is drug-induced interstitial nephritis.
73. The method of claim 64 wherein the kidney disease affects renal tubules.
74. The method of claim 73, wherein the kidney disease which affects renal tubules is selected from the group consisting of: a kidney disease associated with a toxin; a neoplasia; hypersensitivity nephropathy; Sjδgren's syndrome; and AIDS.
75. The method of claim 34, wherein the condition is a smooth muscle cell-dependent disease.
76. The method of claim 75, wherein the smooth muscle cell-dependent disease is a vascular disease.
77. The method of claim 76, wherein the vascular disease is atherosclerosis.
78. The method of claim 75, wherein the smooth muscle cell-dependent disease is a gastrointestinal disease.
79. The method of claim 78, wherein the gastrointestinal disease is selected from the group consisting of esophageal dysmotility, inflammatory bowel disease, and scleroderma.
80. The method of claim 75, wherein the smooth muscle cell-dependent disease is a bladder disease.
81. The method of claim 34, wherein the condition is associated with Epstein-Barr virus.
82. The method of claim 81, wherein the condition is selected from the group consisting of mononucleosis, B cell tumors, Burkitt's lymphoma, and nasopharyngeal carcinoma.
83. The method of claim 34, wherein the treatment does not increase susceptibility of the subject to pneumocystis pneumonia, atypical infections, or tumors.
84. An isolated nucleic acid molecule encoding the protein of claim 1 or 6.
85. The nucleic acid molecule of claim 84, wherein the molecule is DNA.
86. A vector comprising the nucleic acid molecule of claim 84 operably linked to a transcriptional control sequence recognized by a host cell transformed with the vector.
87. The vector of claim 86, wherein the vector is a plasmid.
PCT/US1997/005076 1996-03-21 1997-03-21 Craf1 (traf-3) isoforms and uses thereof Ceased WO1997034473A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU25939/97A AU2593997A (en) 1996-03-21 1997-03-21 Craf1 (traf-3) isoforms and uses thereof

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
US1382096P 1996-03-21 1996-03-21
US60/013,820 1996-03-21
US1662696P 1996-05-01 1996-05-01
US1665996P 1996-05-01 1996-05-01
US60/016,659 1996-05-01
US60/016,626 1996-05-01
US2658496P 1996-09-18 1996-09-18
US60/026,584 1996-09-18

Publications (2)

Publication Number Publication Date
WO1997034473A1 true WO1997034473A1 (en) 1997-09-25
WO1997034473A9 WO1997034473A9 (en) 1998-04-02

Family

ID=27486331

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1997/005076 Ceased WO1997034473A1 (en) 1996-03-21 1997-03-21 Craf1 (traf-3) isoforms and uses thereof

Country Status (2)

Country Link
AU (1) AU2593997A (en)
WO (1) WO1997034473A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999055859A3 (en) * 1998-04-29 2000-02-17 Vlaams Interuniv Inst Biotech Cd40-interacting and traf-interacting proteins
US6410710B1 (en) * 1999-03-11 2002-06-25 The Trustees Of The University In The City Of New York Nucleic acid encoding a TRAF-3 deletion isoform
EP1357131A3 (en) * 1997-01-10 2004-02-11 Biogen, Inc. Treatment of lupus nephritis with anti-CD4OL compounds

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5177085A (en) * 1990-12-13 1993-01-05 Sandoz Ltd. Dihydro-isoquinoline derivatives, processes for their production, pharmaceutical compositions containing them, and their use in treating asthma
US5434248A (en) * 1991-06-21 1995-07-18 Merck & Co., Inc. Peptidyl derivatives as inhibitors of interleukin-1β converting enzyme
US5518729A (en) * 1989-11-22 1996-05-21 Margolin; Solomon B. Compositions and methods for reparation and prevention of fibrotic lesions

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5518729A (en) * 1989-11-22 1996-05-21 Margolin; Solomon B. Compositions and methods for reparation and prevention of fibrotic lesions
US5177085A (en) * 1990-12-13 1993-01-05 Sandoz Ltd. Dihydro-isoquinoline derivatives, processes for their production, pharmaceutical compositions containing them, and their use in treating asthma
US5434248A (en) * 1991-06-21 1995-07-18 Merck & Co., Inc. Peptidyl derivatives as inhibitors of interleukin-1β converting enzyme

Non-Patent Citations (12)

* Cited by examiner, † Cited by third party
Title
ANNU. REV. IMMUNOL., 1994, Vol. 12, BANCHEREAU et al., "The CD40 Antigen and Its Ligand", pages 881-922. *
BLOOD REVIEWS, March 1995, Vol. 9, GORDON J., "CD40 and Its Ligand: Central Players in B Lymphocyte Survival, Growth and Differentiation", pages 53-56. *
BLOOD, June 1995, Vol. 85, No. 10, GRUSS et al., "Tumor Necrosis Factor Ligand Superfamily: Involvement in the Pathology of Malignant Lymphomas", pages 3378-3404. *
CURRENT OPINION IN GENETICS AND DEVELOPMENT, February 1996, Vol. 6, TEWARI et al., "Recent Advances in Tumor Necrosis Factor and CD40 Signaling", pages 39-44. *
FEBS LETTERS, January 1995, Vol. 358, SATO et al., "A Novel Member of the TRAF Family of Putative Signal Transducing Proteins Binds to the Cytosolic Domain of CD40", pages 113-118. *
IMMUNOLOGY TODAY, September 1994, Vol. 15, No. 9, DURIE et al., "The Role of CD40 in the Regulation of Humoral and Cell-Mediated Immunity", pages 406-411. *
J. BIOL. CHEM., December 1994, Vol. 269, HU et al., "A Novel RING Finger Protein Interacts with the Cytoplasmic Domain of CD40", pages 30069-30072. *
J. CELL. BIOCHEM., January 1996, Vol. 60, WARE et al., "Apoptosis Mediated by the TNF-Related Cytokine and Receptor Families", pages 47-55. *
PROC. NATL. ACAD. SCI. U.S.A., December 1995, Vol. 92, MORIO et al., "Characterization of a 23-kDa Protein Associated with CD40", pages 11633-11636. *
SCIENCE, 08 September 1995, Vol. 269, ROTHE et al., "TRAF2-Mediated Activation of NF-kB by TNF Receptor 2 and CD40", pages 1424-1427. *
SCIENCE, 10 March 1995, Vol. 267, CHENG et al., "Involvement of CRAF1, a Relative of TRAF, in CD40 Signaling", pages 1494-1498. *
SEMINARS IN IMMUNOLOGY, October 1994, Vol. 6, FOY et al., "The Expansive Role of CD40 and Its Ligand, gp39, in Immunity", pages 259-266. *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1357131A3 (en) * 1997-01-10 2004-02-11 Biogen, Inc. Treatment of lupus nephritis with anti-CD4OL compounds
WO1999055859A3 (en) * 1998-04-29 2000-02-17 Vlaams Interuniv Inst Biotech Cd40-interacting and traf-interacting proteins
US6812203B1 (en) 1998-04-29 2004-11-02 Vlaams Interuniversitair Instituut Voor Biotechnologie Vzw CD40-Interacting and TRAF-interacting proteins
US6410710B1 (en) * 1999-03-11 2002-06-25 The Trustees Of The University In The City Of New York Nucleic acid encoding a TRAF-3 deletion isoform
US6849415B2 (en) 1999-03-11 2005-02-01 The Trustees Of Columbia University In The City Of New York TRAF-3 deletion isoforms and uses thereof

Also Published As

Publication number Publication date
AU2593997A (en) 1997-10-10

Similar Documents

Publication Publication Date Title
Dürkop et al. Molecular cloning and expression of a new member of the nerve growth factor receptor family that is characteristic for Hodgkin's disease
ES2323392T3 (en) BINDING (ACT-4-L) FOR A RECEIVER LOCATED ON THE SURFACE OF THE ACTIVATED CD4 + T CELLS.
US6475987B1 (en) Tall-1 receptor homologues
JP4411330B2 (en) Tumor necrosis factor-related ligand
TWI322181B (en) Novel baff receptor, nucleic acids encoding same, and uses thereof
US6677135B1 (en) Ret ligand (RetL) for stimulating neutral and renal growth
Gravestein et al. Cloning and expression of murine CD27: comparison with 4‐1BB, another lymphocyte‐specific member of the nerve growth factor receptor family
JP2001520039A (en) Human tumor necrosis factor receptor-like proteins, TR11, TR11SV1 and TR11SV2
JP2002509431A (en) NF-κB receptor activator-receptor is a member of the TNF receptor superfamily
AU7713098A (en) Ntn-2 member of tnf ligand family
AU7608898A (en) Ntn-2 member of tnf ligand family
RS51602B (en) APRIL RECEPTOR (BCMA) AND ITS USE
US20030044416A1 (en) Nucleic acids encoding cd100 molecules
US6822070B2 (en) Truncated CRAF1 inhibits CD40 signaling
WO1999007738A2 (en) Human orphan receptor ntr-1
US6274362B1 (en) RGS-containing molecules and uses thereof
WO2001016169A2 (en) RET LIGAND 5 (Retl5) FROM HUMAN AND MOUSE
WO1997034473A1 (en) Craf1 (traf-3) isoforms and uses thereof
WO1997034473A9 (en) Craf1 (traf-3) isoforms and uses thereof
EP4653455A1 (en) Mutated pd1 ectodomain fragment and car containing same, and nk cell
WO2000069880A1 (en) Il-9/il-2 receptor-like molecules and uses thereof
WO1999026980A1 (en) Methods and reagents for the utilization of sap family member proteins, novel signal transduction regulators
US7235632B1 (en) Isolated mammalian protein present at the surface of all lymphoid progenitor cells and all mature NK cells and uses thereof
CA2316545A1 (en) Novel nucleic acid and polypeptide with homology to the tnf-receptors
WO2000012762A1 (en) A novel protein related to melanoma-inhibiting protein and uses thereof

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU CA JP MX US US US US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
COP Corrected version of pamphlet

Free format text: PAGES 9 AND 89, DESCRIPTION, PAGES 117-123, CLAIMS, AND PAGES 20/30 AND 24/30, DRAWINGS, REPLACED BY NEW PAGES BEARING THE SAME NUMBER; DUE TO LATE TRANSMITTAL BY THE RECEIVING OFFICE

NENP Non-entry into the national phase

Ref country code: JP

Ref document number: 97533795

Format of ref document f/p: F

122 Ep: pct application non-entry in european phase