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WO1999002709A1 - Proteines hybrides recombinees d'erythropoietine / immunoglobuline - Google Patents

Proteines hybrides recombinees d'erythropoietine / immunoglobuline Download PDF

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Publication number
WO1999002709A1
WO1999002709A1 PCT/US1998/013930 US9813930W WO9902709A1 WO 1999002709 A1 WO1999002709 A1 WO 1999002709A1 US 9813930 W US9813930 W US 9813930W WO 9902709 A1 WO9902709 A1 WO 9902709A1
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Prior art keywords
erythropoietin
fusion protein
constant region
immunoglobulin
immunoglobulin constant
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.)
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PCT/US1998/013930
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English (en)
Inventor
Arthur J. Sytkowski
Terry B. Strom
Xin Xiao Zheng
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Beth Israel Deaconess Medical Center Inc
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Beth Israel Deaconess Medical Center Inc
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Priority to AU81822/98A priority Critical patent/AU8182298A/en
Publication of WO1999002709A1 publication Critical patent/WO1999002709A1/fr
Anticipated expiration legal-status Critical
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    • 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
    • C07K14/475—Growth factors; Growth regulators
    • C07K14/505—Erythropoietin [EPO]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide

Definitions

  • Erythropoietin is a glycoprotein hormone involved with the growth and development of mature red blood cells from erythrocyte precursor cells. It is a 166 amino acid polypeptide that exists naturally as a monomer. (Lin, F-K., et al . , Proc . Na tl . Acad. Sci . USA 82:7580-7584 (1985)) .
  • Erythropoietin is typically administered by intravenous or subcutaneous injection three times weekly at a dose of approximately 25-100 U/kg.
  • erythropoietin therapy is that, although quite effective, this form of therapy is very expensive.
  • Estimated costs for the treatment of chronic dialysis patients have ranged from $8,000-10,000 per patient per year.
  • erythropoietin has a relatively short plasma half-life (Spivak, J.L., and Hogans, B.B., Blood, 73: 90 (1989); McMahon, F.G., et al . , Blood,
  • the present invention relates to fusion proteins comprising erythropoietin or erythropoietin-like molecules, and immunoglobulin polypeptide chains.
  • the fusion proteins described herein are referred to as erythropoietin/immunoglobulin fusion proteins, or erythropoietin fusion proteins.
  • the erythropoietin fusion proteins of the present invention have increased biological activity wherein biological activity is defined as an increased in vivo half-life relative to wild type, or naturally-occurring, erythropoietin.
  • the erythropoietin fusion proteins of the present invention can also exhibit increased biological activity as manifested by an increase in stimulation of hematopoiesis when compared to wildtype erythropoietin. Such biological activity can be independent of an increased in vivo half-life, or in addition to increased in vivo half-life. Because the erythropoietin/immunoglobulin fusion proteins of the present invention have increased biological activity, the frequency with which they must be administered is reduced from the frequency of administration of naturally-occurring erythropoietin.
  • erythropoietin fusion protein of the present invention if erythropoietin fusion protein of the present invention is used, a reduced quantity of erythropoietin fusion protein over the course of treatment of an individual would be necessary than if naturally- occurring erythropoietin is used.
  • the immunoglobulin polypeptide chains of the present invention comprise the constant region of the immunoglobulin molecule.
  • the chains can comprise either the heavy chain constant region or both the heavy and light chain constant regions, also referred to herein as immunoglobulin constant and light chain domains.
  • the present invention also relates to multimers (also referred to herein as oligomers) of erythropoietin/immunoglobulin fusion proteins comprising two or more, e.g., four, erythropoietin/Ig fusion protein monomers, typically joined by interchain covalent linkages, such as disulfide bonds.
  • erythropoietin/Ig fusion proteins referred to herein as dimers (if two monomers are joined) , or tetrameres (if four monomers are joined) , also exhibit the increased biological activity described herein.
  • dimers if two monomers are joined
  • tetrameres if four monomers are joined
  • an erythropoietin/immunoglobuin fusion protein wherein an erythropoietin molecule replaces the V L and V H chains of the immunoglobulin.
  • DNA encoding erythropoietin, or an erythropoietin-like molecule is fused at its N-terminus to DNA encoding an immunoglobulin constant region.
  • DNA encoding erythropoietin, or an erythropoietin-like molecule is fused at its C-terminus to the DNA encoding an immunoglobulin constant region. The fused sequence is expressed in competent cells, resulting in production of an erythropoietin/immunoglobulin fusion protein that has biological activity.
  • the erythropoietin, or erythropoietin-like molecule is modified to remove carbohydrate chains, or the erythropoietin, or erythropoietin-like molecule, is mutated to alter, or delete, naturally-occurring glycosylation sites from the molecule.
  • DNA encoding non-glycosylated erythropoietin, or non-glycosylated erythropoietin-like molecule is then fused to DNA encoding an immunoglobulin constant region.
  • DNA encoding erythropoietin can be mutated to increase biological activity (e.g., alanine 101 erythropoietin) and fused to DNA encoding an immunoglobulin constant region.
  • DNA encoding an immunoglobulin constant region is typically modified to substantially decrease or eliminate Fc receptor binding or complement fixing activity.
  • nucleic acids encoding the fusion proteins described herein and their encoded amino acid sequences.
  • the present invention further relates to methods of producing the erythropoietin/immunoglobulin fusion proteins with increased biological activity described herein, and to methods of their use, for example, in the treatment of anemia.
  • fusion protein compositions comprising erythropoietin and immunoglobulin, which exhibit increased biological activity relative to wild type erythropoietin, are now available.
  • the erythropoietin fusion proteins of the present invention can be di erized, or tetramerized, with additional erythropoietin fusion proteins to produce multimeric erythropoietin fusion proteins with prolonged in vivo half- life.
  • the present invention relates to the production and use of erythropoietin/immunoglobulin fusion proteins with increased biological activity.
  • the erythropoietin/ immunoglobulin fusion proteins described herein are also referred to as erythropoietin/immunoglobulin chimeras, chimeric protein or hybrid proteins.
  • the erythropoietin/immunoglobulin fusion proteins of the present invention comprise polypeptides having two components: erythropoietin, or an erythropoietin-like molecule, (defined herein as an erythropoietin fragment, analog, variant, mutant or derivative of erythropoietin) , and the constant region of an immunoglobulin, or a fragment, analog, variant, mutant or derivative of the immunoglobulin.
  • the fusion protein can also comprise one or more additional components, such as signal or targeting sequences.
  • the first component of the fusion protein is erythropoietin, which is a protein hormone involved with the growth and development of red blood cells from erythrocyte precursor cells. Erythropoietin is produced in the kidney in response to hypoxia (e.g., red blood cell loss due to anemia) and regulates red blood cell growth and differentiation through interaction with its cognate cellular receptor. Wild type, or naturally-occurring, erythropoietin is defined herein to include recombinant erythropoietin (Jacobs, K. , et al . , Nature, 313:806-813
  • Erythropoietin is a 166 amino acid polypeptide that exists naturally as a monomer. The predicted secondary structure of erythropoietin has been reported (McDonald, J.D., et al . , Mol . Cell . Biol . , 5:842-848 (1986)).
  • erythropoietin also encompasses biologically active fragments of erythropoietin, erythropoietin mutants (also referred to herein as muteins) and erythropoietin analogs, variants and derivatives, referred to herein as erythropoietin-like molecules.
  • the biological activity of erythropoietin is defined as the ability to regulate red blood cell growth and differentiation through interaction with its cognate cellular receptor, or the antigenic property of inducing a specific immunological response as determined using well-known laboratory techniques.
  • a biologically active, or functionally active, fragment of erythropoietin can induce an immunological response which produces antibodies specific for erythropoietin (anti-erythropoietin antibodies) .
  • an erythropoietin-like molecule typically shares substantial sequence (amino acid) similarity (e.g., at least about 65%, typically at least about 80% and most typically about 90- 95%) with the corresponding sequences of wild type, or naturally-occurring, erythropoietin and possesses one or more of the functions of wild type erythropoietin thereof.
  • the erythropoietin of the present invention is understood to specifically include erythropoietin polypeptides having amino acid sequences analogous to the sequence of the wild type erythropoietin.
  • Such proteins are defined herein as erythropoietin analogs.
  • An "analog” is defined herein to mean an amino acid sequence with sufficient similarity to the amino acid sequence of wild type erythropoietin to possess the biological activity of the protein.
  • an analog of a polypeptide can contain "silent" changes in the nucleic acid sequence which encodes a polypeptide, wherein one or more amino acid residues differ from the amino acid sequence of wild type erythropoietin, yet possesses, e.g., the ability to stimulate red blood cell production or maturation. Examples of such differences include additions, deletions or substitutions of residues.
  • proteins that exhibit greater or lesser biological activity of wild type erythropoietin such as described in U.S. Patent No. 5,614,184, the teachings of which are incorporated herein by reference.
  • Exemplary mutant erythropoietin molecules with either increased or decreased biological activity as described in U.S. Patent No. 5,614,184 include, for example, alanine 101 erythropoietin; alanine 103 erythropoietin; alanine 104 erythropoietin; alanine 105 erythropoietin and alanine 108 erythropoietin.
  • the present invention also encompasses biologically active fragments of erythropoietin.
  • Such fragments can include only a part of the full-length amino acid sequence of erythropoietin yet possess biological activity.
  • a "biologically active fragment” means a fragment that can exert a biological or physical effect of the full- length protein, or has a biological characteristic, e.g., antigenicity, of the full-length protein.
  • a biologically active erythropoietin fragment can induce the growth and differentiation of red blood cells or stimulate an immunogenic response.
  • the antigenicity of a peptide fragment can be determined, for example, as described in Geysen, et al .
  • Such fragments can be produced by amino and carboxyl terminal deletions as well as internal deletions. Also included are active fragments of the protein as obtained by enzymatic digestion. Such peptide fragments can be tested for biological activity as described herein.
  • erythropoietin proteins that have been modified. They include erythropoietin polypeptides that have been modified by alterations in their amino acid sequence. They also include truncated and hybrid forms of erythropoietin. "Truncated” forms are shorter versions of erythropoietin, for example, with amino terminal, or carboxyl terminal residues removed. Variants can be produced using methods discussed below.
  • the erythropoietin gene can be mutated in vi tro or in vivo using techniques well known to those of skill in the art, for example, site-specific mutagenesis and oligonucleotide mutagenesis. (See for example, U.S. Patent NO. 5,614,184.) Manipulations of erythropoietin can be made at the protein level as well. Any of numerous chemical modifications can be carried out by known techniques including, but not limited to, specific chemical cleavage by cyanogen bromide, trypsin and papain.
  • mutations can be conservative or non- conservative amino acid substitutions, amino acid insertions or amino acid deletions.
  • DNA encoding an erythropoietin amino acid sequence variant is prepared by site-directed mutagenesis of DNA that encodes a variant or a nonvariant version of erythropoietin.
  • Site- directed (site-specific) mutagenesis allows the production of erythropoietin variants through the use of specific oligonucleotide sequences that encode the desired mutation, as well as a sufficient number of adjacent nucleotides, to provide a primer sequence of sufficient size and sequence complexity to form a stable duplex on both sides of the deletion junction being traversed.
  • a primer of about 20 to 25 nucleotides in length is preferred, with about 5 to 10 residues on both sides of the junction of the sequence being altered.
  • the site-specific mutagenesis technique typically employs a phage vector that exists in both a single-stranded and double-stranded form.
  • Typical vectors useful in site-directed mutagenesis include vectors such as the M13 phage, for example, as disclosed by Messing et al . , Third Cleveland Symposium on Macromolecules and Recombinant DNA, A.
  • phage vectors are commercially available and their use is well-known to those skilled in the art.
  • a versatile and efficient procedure for the construction of oligonucleotide directed site-specific mutations in DNA fragments using M13-derived vectors was published by Zoller, M.J. and Smith, M. , Nucleic Acids Res . 10:6487-6500 (1982)).
  • Plasmid vectors that contain a single-stranded phage origin of replication can also be employed to obtain single-stranded DNA. Veira et al . , Meth . Enzymol . 153:3 (1987) .
  • nucleotide substitutions can be introduced by synthesizing the appropriate DNA fragment in vitro, and amplifying it by PCR procedures known in the art .
  • site-specific mutagenesis can be performed by first obtaining a single-stranded vector that includes within its sequence a DNA sequence that encodes the relevant protein.
  • An oligonucleotide primer bearing the desired mutated sequence is prepared, generally synthetically, for example, by the method of Crea, et al . , Proc. Natl . Acad. Sci . USA 75, 5765 (1978).
  • This primer can then be annealed with the single-stranded protein sequence-containing vector, and subjected to DNA- polymerizing enzymes such as E. coli polymerase I Klenow fragment, to complete the synthesis of the mutation-bearing strand.
  • heteroduplex is formed wherein one strand encodes the original non-mutated sequence and the second strand bears the desired mutation.
  • This heteroduplex vector can then be used to transform appropriate host cells such as JM101 cells, and clones can be selected that include recombinant vectors bearing the mutated sequence arrangement. Thereafter, the mutated region can be removed and placed in an appropriate expression vector for protein production.
  • the PCR technique can also be used in creating amino acid sequence variants of an erythropoietin polypeptide.
  • primers that differ slightly in sequence from the corresponding region in a template DNA can be used to generate relatively large quantities of a specific DNA fragment that differs from the template sequence only at the positions where the primers differ from the template.
  • one of the primers can be designed to overlap the position of the mutation and to contain the mutation.
  • the sequence of the other primer is preferably identical to a stretch of sequence of the opposite strand of the plasmid, but this sequence can be located anywhere along the plasmid DNA.
  • the sequence of the second primer is located within 500 nucleotides from that of the first, such that in the end the entire amplified region of DNA bounded by the primers can be easily sequenced.
  • PCR amplification using a primer pair as described above results in a population of DNA fragments that differ at the position of the mutation specified by the primer, and possibly at other positions, as template copying is somewhat error-prone. If the ratio of template to product material is extremely low, the vast majority of product DNA fragments incorporate the desired mutation (s). This product can be used to replace the corresponding region in the plasmid that served as PCR template using standard DNA technology.
  • Mutations at separate positions can be introduced simultaneously by either using a mutant second primer or performing a second PCR with different mutant primers and ligating the two resulting PCR fragments simultaneously to the vector fragment in a three (or more) part ligation.
  • Another method for preparing variants, cassette mutagenesis is based on the technique described by Wells et al . Gene 34, 315 (1985) .
  • the starting material can be the plasmid (or vector) comprising the erythropoietin DNA to be mutated.
  • the codon(s) within the erythropoietin to be mutated are identified. There must be unique restriction endonuclease sites on each side of the identified mutation site(s).
  • restriction sites do not exist, they can be generated using the above-described oligonucleotide-mediated mutagenesis method to introduce them at appropriate locations in the erythropoietin DNA. After the restriction sites have been introduced into the plasmid, the plasmid is cut at these sites to linearize it.
  • a double stranded oligonucleotide encoding the sequence of the DNA between the restriction sites but containing the desired mutation (s) is synthesized using standard procedures. The two strands are synthesized separately and then hybridized together using standard techniques. This double-stranded oligonucleotide is referred to as the cassette.
  • This cassette is designed to have 3' and 5 1 ends that are compatible with the ends of the linearized plasmid, such that it can be directly ligated to the plasmid.
  • This plasmid now contains the mutated erythropoietin DNA sequence, that can be expressed to produce mutated erythropoietin.
  • Naturally-occurring erythropoietin is glycosylated at three N-linked positions and one O-linked position.
  • fusion proteins comprising non- glycosylated erythropoietin, or non-glycosylated erythropoietin-like molecules, and an immunoglobulin constant region polypeptide.
  • Non-glycosylated erythropoietin is defined herein as erythropoietin lacking N-linked and/or O-linked carbohydrates (oligosaccharide chains) .
  • Site-directed mutagenesis can be used to alter or eliminate the carbohydrate attachment sites or erythropoietin, for example, as described in Dube, S., et al . , J. Biol . Chem . , 253:17516-17521 (1988).
  • carbohydrates can be enzymatically removed from erythropoietin, using techniques well-known to those of skill in the art, such as N-glycanase digestion.
  • Immunoglobulins are stable plasma proteins with substantial half-lives.
  • An immunoglobulin constant region polypeptide, or a fragment, mutant, analog or variant thereof, fused to non-glycosylated erythropoietin can reasonably extend the plasma half-life of non-glycosylated erythropoietin, e.g., a plasma half-life of at least two times greater than the half life of the non-fused, non-glycosylated erythropoietin .
  • the second component of the fusion protein of the present invention is the constant region of an immunoglobulin.
  • the erythropoietin molecule can be fused to the immunoglobulin constant domain at either its C-terminus or its N-terminus.
  • the C-terminus of erythropoietin is fused to the N-terminus of an immunoglobulin constant region polypeptide, (e.g. N-Epo- C-N-Ig-C, where the erythropoietin molecule is located upstream of the Ig constant region) .
  • the C-terminus of the immunoglobuin constant region is fused to the N-terminus of erythropoietin (e.g., N-Ig-C-N-Epo-C, where the erythropoietin molecule is located downstream of the Ig constant region) .
  • erythropoietin e.g., N-Ig-C-N-Epo-C, where the erythropoietin molecule is located downstream of the Ig constant region
  • biologically active fragments, analogs, mutants, variants and derivatives of immunoglobulin are described above.
  • the biological activity of an immunoglobulin fragment, analog, mutant, variant or derivative is the ability of the immunoglobulin fragment, analog, mutant, variant or derivative to extend the in vivo half-life of the fused erythropoietin molecule, or to enhance the potency of the fused erythropoietin.
  • the enhanced potency of erythropoietin results from, e.g., the use of oligomerized rather than monomeric erythropoietin.
  • Use of oligomerized erythropoietin can stimulate the activity of the erythropoietin receptor, which must be oligomerized to induce intracellular or signaling, resulting in growth and differentiation of red blood cells.
  • the fusion protein acts as an erythropoietin agonist.
  • Immunoglobulin and biologically active fragments, analogs, mutants, variants and derivatives thereof, are well-known to those of skill in the art.
  • the classes of immunoglobulin are IgG, IgD, IgA, IgE and IgM.
  • the IgG class is subdivided into subclasses IgGl, IgG2, IgG3 and IgG4. These subclasses are further sub-divided, e.g., IgG2a.
  • IgA is divided into subclasses IgAl and IgA2.
  • Immunoglobulin comprises heavy and light polypeptide chains.
  • the Fc portion of the immunoglobulin is defined as a naturally-occurring or synthetically produced polypeptide homologous to the immunoglobulin C-terminal domain that is produced upon papain digestion.
  • the constant region of the heavy chains of all mammalian immunoglobulin exhibit extensive amino acid sequence similarity.
  • the constant region domains are termed CHI, CH2 and CH3.
  • a "hinge" region joins CHI to CH2-CH3.
  • the hinge region typically comprises the polypeptide homologous to the naturally-occurring immunoglobulin region which includes the cysteine residues at which disulfide bonds form which link the two heavy chains of the immunoglobulin.
  • hinge regions for human and mouse immunoglobulin can be found in ANTIBODY ENGINEERING, A PRACTICAL GUIDE, Borrebaeck, C. A. K. , ed., W. H. Freeman and Co., 1992, the teachings of which are herein incorporated by reference.
  • the entire immunoglobulin heavy chain constant region (CHl-hinge-CH2-CH3) can be fused to the erythropoietin molecule.
  • the immunoglobulin constant region can comprise all, or a portion of the hinge region, the CH2 domain and the CH3 domain.
  • the immunoglobulin constant region can also comprise the CLl domain of an immunoglobulin light chain.
  • the polypeptide can be altered, or mutated, to eliminate, or significantly decrease complement fixation activity and/or Fc receptor binding.
  • the amino acid residues which comprise the Fc binding site, or the Clq binding site, of the immunoglobulin constant region amino acid sequence can be deleted or mutated, thereby eliminating, or substantially decreasing Fc binding or Clq binding.
  • the fusion proteins of the present invention are typically produced by recombinant methods well-known to those of skill in the art. (See e.g., Morrison, S.L., Science, 229:1202-1207 (1985); Mark, M.R., et al . , J.
  • nucleic acid construct comprising a nucleic acid sequence encoding erythropoietin, or a fragment, mutant, variant or analog thereof, joined to a nucleic acid sequence encoding the hinge region, CH2 and CH3 domains of an immunoglobulin constant region.
  • Nucleic acid sequences encoding immunoglobulin are known to those of skill in the art. Such sequences can be obtained from cDNA libraries or synthetically produced.
  • the erythropoietin/Ig nucleic acid construct can be introduced into an expression vector by methods well-known to those of skill in the art and introduced into a competent cell (e.g., a cell that is compatible with the vector sequences and capable of expressing the encoded fusion protein) which then expresses the erythropoietin/immunoglobulin fusion protein.
  • a competent cell e.g., a cell that is compatible with the vector sequences and capable of expressing the encoded fusion protein
  • cDNA for V L can be excised and cDNA sequence encoding erythropoietin, or a fragment, analog, mutant, variant or derivative thereof, is placed upstream of the constant region of an immunoglobulin light chain.
  • An erythropoietin/Fc ⁇ 2a sequence and an erythropoietin CLl sequence are then co-transfected into a competent mammalian cell, resulting in the production of a tetrameric erythropoietin/Ig fusion protein.
  • the amino acid sequence comprising the fusion protein can be synthesized by methods well-known to those of skill in the art.
  • the erythropoietin molecule can be joined to the Ig sequence at either the N-terminus or C-terminus of erythropoietin.
  • the precise site of joining the nucleic acid sequence encoding erythropoietin to the nucleic acid sequence encoding the immunoglobulin constant region can be determined by one of skill in the art by routine experimentation. Such sites are known.
  • the nucleic acid sequence encoding erythropoietin and the nucleic acid sequence encoding the immunoglobulin constant region must be in the correct translational reading frame.
  • the erythropoietin nucleic acid sequence can be joined directly to, e.g., the hinge region nucleic acid sequence, or, alternatively, additional nucleotides encoding a flexible protein sequence, (e.g., about 1 to about 20 amino acids) can be inserted prior to the hinge region nucleic acid sequence, as long as the inserted nucleotides do not interfere with the biological activity of the expressed fusion protein or do not confer any undesired activities, e.g., such as antigenity.
  • additional nucleotides encoding a flexible protein sequence e.g., about 1 to about 20 amino acids
  • Nucleic acid sequences encompassed by the present invention include isolated and/or recombinant nucleic acid sequences which encode the erythropoietin/Ig fusion protein. Also encompassed by the present invention are nucleic acid sequences (DNA or RNA) which are substantially complementary to the sequences encoding the erythropoietin/Ig fusion proteins and nucleic acid sequences which hybridize with the erythropoietin/Ig fusion protein nucleic acid sequences. Hybridization conditions sufficient to identify nucleic acid sequences with substantial sequence identity to the erythropoietin/Ig fusion proteins of the present invention are known to those of skill in the art.
  • substantially complementary means that the sequence need not reflect the exact sequence of the erythropoietin/Ig fusion protein, but must be sufficiently similar in identity to hybridize with the sequences of the present invention.
  • non- complementary bases, or additional bases can be interspersed in the sequences provided that the sequence has sufficient complementary bases to hybridize therewith.
  • the expressed erythropoietin/immunoglobulin fusion proteins are secreted from cells transformed with the DNA construct into the cell culture medium.
  • the secreted fusion protein can be secreted as a single chain polypeptide, also referred to herein as a monomer.
  • the fusion protein can associate via covalent or noncovalent (e.g., disulfide or hydrophobic) interactions to form multimeric fusion proteins, such as dimers or tertramers, which are also secreted into the culture medium.
  • the immunoglobulin constant region contains cysteine amino acid residues. Two fusion protein monomers containing cysteine residues can form interchain disulfide bonds, resulting in fusion protein dimers.
  • These secreted fusion proteins can be recovered form the culture medium using techniques well- known to those of skill in the art.
  • the preferred host cells are eukaryotic cells, e.g., mammalian cells such as CHO or COS.
  • the fusion protein can contain glycosylation sites that are substantially the same as naturally-occurring erythropoietin and immunoglobulin, or the glycosylation of the fusion protein can vary from that of the naturally-occurring proteins.
  • the glycosylation pattern can vary from the pattern of glycosylation obtained when the fusion protein is produced in mammalian cells.
  • Erythropoietin has a relatively short plasma half-life (Spivak, J.L. and Hogans, B.B., Blood, 73:90-99 (1989); McMahon, F.G., et al . , Blood, 76:1718-1722 (1990).
  • the erythropoietin/immunoglobulin fusion proteins of the present invention reasonably have an increased circulating in-vivo half-life.
  • the increase in circulating half-life is extended by a factor of two or more when compared to naturally-occurring erythropoietin.
  • the in vivo half-life can be extended from minutes (as is typical with naturally-occurring erythropoietin) to hours or even days, with the fusion proteins described herein.
  • Circulating half-life of the fusion proteins of the present invention can be tested using methods known to those of skill in the art.
  • the erythropoietin/immunoglobulin fusion protein can be injected into rabbits, and blood samples analyzed at specific time points.
  • the biological activity of the erythropoietin component circulating as fusion protein present in the blood samples can be assayed by known methods, such as the Krystal bioassay (Krystal, G. Exp . Hema tol . , 11:649-660 (1993), the teachings of which are herein incorporated by reference.
  • structural integrity of the erythropoietin fusion protein can be measured by reactivity with erythropoietin-specific antibodies such as described in Sytkowski, A.J. and Fisher, J.W., J. Biol . Chem . , 260:14727-14731, the teachings of which are herein incorporated by reference.
  • the prolonged circulating half-life of the erythropoietin fusion protein is reasonably due to its increased size relative to monomeric erythropoietin, which would hinder its excretion from the body through the kidney, and reduce clearance by other mechanisms.
  • erythropoietin/immunoglobulin fusion proteins which exhibit increased biological activity associated with prolonged in vivo half-life, or increased potency.
  • This increase in biological activity indicates that an effective amount of erythropoietin/immunoglobulin fusion protein is substantially less than a comparable effective amount of naturally-occurring erythropoietin.
  • the effective amount of erythropoietin is defined herein as the amount of erythropoietin required to elicit an erythropoietic response, as indicated by increased growth and/or differentiation of erythrocytic precursor cells.
  • the effective amount of erythropoietin fusion protein described herein will require less frequent administration than an equivalent amount of naturally-occurring erythropoietin.
  • a reduced quantity of erythropoietin, administered as erythropoietin/Ig fusion protein will be required over the course of treatment than is necessary if wild type erythropoietin is used.
  • the erythropoietin/immunoglobulin fusion protein with increased biological activity described herein can be used in place of wild type erythropoietin whenever treatment with erythropoietin is called for.
  • the EPO/Ig fusion protein is used to treat an individual with a hematopoietic disease or deficiency.
  • erythropoietin fusion protein can be used for treatment in an individual experiencing anemia associated with renal failure, chronic disease, HIV infection, blood loss or cancer.
  • Erythropoietin is generally administered to humans. Effective treatment with erythropoietin requires maintaining a therapeutic blood level. This can be done by continuous administration, that is, by continuous intravenous injections, by discreet intravenous injections, or by subcutaneous injection.
  • the erythropoietin/Ig fusion protein of this invention can be employed in admixture with conventional excipients, i.e., pharmaceutically acceptable organic or inorganic carrier substances suitable for parenteral administration that do not deleteriously react with the active derivatives, referred to herein as pharmaceutical compositions.
  • Suitable pharmaceutically acceptable carriers include, but are not limited to, water, salt solutions, alcohols, gum arabic, vegetable oils, benzyl alcohols, polyethylene glycols, gelatine, carbohydrates such as lactose, amylose or starch, magnesium stearate, talc, silicic acid, viscous paraffin, perfume oil, fatty acid esters, hydroxymethy- cellulose, polyvinyl pyrrolidone, etc.
  • injectable, sterile solutions preferably oily or aqueous solutions, as well as suspensions, emulsions, foams, or implants, including suppositories .
  • the actual preferred amounts of active compound in a specific case will vary according to the specific compound being utilized, the particular compositions formulated, the mode of application, the particular situs of application, and the individual being treated. Dosages for a given recipient will be determined on the basis of individual characteristics, such as body size, weight, age, gender and the type and severity of the condition being treated.
  • the erythropoietin fusion protein of the present invention with increased biological activity, can be used in any in vi tro application in place of wild type erythropoietin.
  • modified erythropoietin can be used in studies of erythropoietin receptor activity.
  • the amount of erythropoietin fusion protein with increased biological activity needed to achieve desired results (e.g., increased hemoglobinization of red blood cell precursor cells) will be less than the amount of wild type erythropoietin required to achieve those desired results.
  • EXEMPLIFICATION PRODUCTION OF AN ERYTHROPOIETIN/ IMMUNOGLOBULIN FUSION PROTEIN
  • An erythropoietin/immunoglobulin fusion protein can be produced according to the methods described in Steurer, W., et al . , J. Immunol . , 155:1165-1175 (1995), the teachings of which are incorporated, in their entirety, by reference.
  • a brief description of a method of producing an Epo/Fc ⁇ 2a heavy chain chimeric fusion protein follows.
  • the fusion protein is expected to bind to its receptor, but not target antigen presenting cells (APCs) for lysis through antibody-cellular cytotoxicy (ADCC) or complement-directed cytolysis (CDC) .
  • APCs target antigen presenting cells
  • rat anti-mouse IgG2a (PharmMingen, San Diego, CA, rat anti- mouse Ig2a-horseradish peroxidase (PharMingen) , FITC- labeled goat anti-mouse IgG (Sigma Chemical Co., St. Louis, MO) , biotinylated rabbit anti-rat mAb (Vector, Burlingame, CA) , FITC-rabbit anti-hamster IgG (Pierce, Rockford, IL) , and mouse IgG2a (k) and IgG3 (k) hybridoma proteins (Cappel, West Chester, PA) .
  • the following cell lines are used: murine IgG2a- secreting hybridoma 116-13.1 (American Type Culture Collection (ATCC) , Rockville, MD) , CHO-K1 (ATCC) .
  • CHO cells transfected with human Fc ⁇ RI cDNA, and transfected CHO cells are described in Steurer, W. , et al . , J. immunol . , 255:1165-1175 (1995), and can be produced using standard laboratory techniques.
  • the eukaryotic expression vector Rc/CMV (Invitrogen, San Diego, CA) , is modified by deletion of all three BamHl sites and its unique Apal site.
  • the PCT II vector (Invitrogen) is used for TA cloning of cDNA amplified by the PCR.
  • RNA is purified on a cesium chloride (Life Technologies, Inc.) gradient, from the murine IgG2a- secreting hybridoma 116-13.1 and then reverse cDNA using oligo-dT 12-18 (Pharmacia, Piscataway, NJ) primers and M- MLV reverse transcriptase (Life Technologies Inc.).
  • the region of the Fc ⁇ 2a cDNA encoding the hinge, CH2 and CH3 domains of the heavy chain is then amplified by PCR using oligonucleotides designed to append unique BamHI and Xbal restriction sites onto the 5' and 3' enzymes (New England Biolabs, Beverly, MA) and gel purified in preparation for ligation (see below) .
  • a cDNA encoding the erythropoietin is amplified by PCR using oligonucleotides designed to append unique NotI and BamHI restriction sites onto the 5' and 3' ends of this cDNA PCR respectively.
  • the cDNA is then cloned into the PCR II vector, excised using NotI (New England Biolabs) and BamHI restriction endonucleases, and gel purified.
  • the erythropoietin cDNA, the previously prepared Fc ⁇ 2a cDNA, and the cDNA of the modified Rc/CMV vector opened at the cloning site with NotI and .Xbal restriction endonucleases are mixed and ligated using T4 DNA ligase (Life Technologies, Inc.). The correct reading frame at the junction of the erythropoietin to Fc CDNAs is confirmed by DNA sequencing.
  • PCR-assisted, site-directed mutagenesis of the Fc ⁇ 2a cassette is used to render nonfunctional (a) the high affinity Fc ⁇ RI receptor binding site by substituting Glu for Leu 235, localization of the binding site for the human high-affinity Fc receptor on IgG. (Duncan, A.R., et al . , Na ture 332:563 (1988)) and (b) the Clq binding site by substituting Glu 318, Lys 322 with Ala residues, the binding site for Clq on IgG (Duncan, A.R., and Winter, G., Na ture 332:738 (1988)).
  • the cDNA mutations are confirmed by Dna sequencing. Subsequence expression of these constructs results in erythropoietin/Fc fusion proteins with or without ADCC and CDC activity, respectively.
  • 20 ⁇ g of the murine EPO/Ig plasmid construct is linearized by Pvu I digestion (New England Biolabs) and electroporated into 10 7 CHO-K1 cells.
  • Transformed CHO-K1 cells are selected with 1 mg/ml G418 (Life Technologies, Inc.), and subsequently cloned by limiting dilution.
  • Established cell lines are then screened for EPO/Ig production by an ELISA specific for murine IgG2a. High producing clones are cultured in serum- free media for 12 days.
  • COS I cells are grown to 70% confluency in Dulbecco's Modified Eagle Medium, high glucose (4.5 g/L; Gibco) , 10% fetal bovine serum (Hyclone) in the presence of 100 U penicillin, 100 ⁇ g streptomycin, 250 ng Fungizone per ml of tissue culture medium (antibiotic-antimycotic cocktail from Gibco) at 37°C and 10% C0 2 .
  • the cells are harvested by trypsinizing using 0.05% Trypsin, 0.53 mM EDTA (Gibco) and washed twice with phosphate buffered saline (PBS)/6mM glucose solution.
  • PBS phosphate buffered saline
  • CHO Chinese Hamster Ovary cells
  • NS.l myeloma cells can be used for stable expression of Epo/Ig protein.
  • CHO cells are grown to 70% confluency in Dulbecco's Modified Eagle Medium, high glucose (4.5 g/L; Gibco), 10% fetal bovine serum (Hyclone) in the presence of 100 U penicillin, 100 ⁇ g streptomycin, 250 ng Fungizone per ml of tissue culture medium (antibiotic-antimycotic cocktail from Gibco) at 37°C and 10% C0 2 .
  • the cells are harvested by trypinsizing using 0.05% Trypsin, 0.53 mM EDTA (Gibco) and washed twice with phosphate buffered saline (PBS)/6mM glucose solution. Cells are suspended in the above PBS/glucose buffer to a concentration of 2 X 10 6 cells/ml. 0.5 ml. of cells placed in electroporation cuvettes (0.4 cm gap, Bio-Rad) and 20 ⁇ g of linearized pcDNA/EPO/hinge/EPO plasmid DNA is added.
  • Cells are plated in 30 ml. of pre- warmed DMEM, high glucose, 10% FBS containing 1.5 mg/ml of G418 (Geneticin, Gibco BRL) and incubated at 37°C and 5% C0 2 . After subcloning, high producing clones are selected by screening supernatants for EPO by ELISA (PharMingen, San Diego, CA) . The control is 10 ⁇ g of pcDNA-EPO.
  • Affinity-purified proteins are characterized by Laemmeli gel electrophoresis under reducing (+DTT) and nonreducing (-DTT) conditions. After transfer to a nylon membrane (Imobilon-P, Millipore, Bedford, MA) the protein is: 1) visualized by Coomassie blue staining, and 2) analyzed by Western blot to confirm the IgG2a isotype specificity using a rat ant-mouse IgG2a as the primary Ab, a biotinylated rabbit anti-rat mAb as the secondary Ab, and visualized with avidin-HPRO complex (Vector) using 3 ',3'- diaminobenzidine (DAB; Vector) for detection of enzyme activity.
  • DOTA 3 ',3'- diaminobenzidine
  • Erythropoietin-activity of the EPO/Ig fusion protein is assayed as described in U.S. Patent 5,580,853, the teachings of which are hereby incorporated by reference.
  • Samples of fusion protein are evaluated for biological activity according to the method of Krystal, G., Exp. Hematal., 11: 649-660 (1983). Briefly, the bioassay of Krystal measures the effect of erythropoietin on intact mouse spleen cells. Mice are treated with phenylhydrazine to stimulate production of red blood cell precursor cells in the spleen.
  • spleens After treatment, the spleens are removed, intact spleen cells are carefully isolated and incubated with various amounts of wild type erythropoietin or the modified erythropoietin described herein. After an overnight incubation, 3 H thymidine is added and its incorporation into cellular DNA is measured. The amount of 3 H thymidine incorporation is indicative of erythropoietin- stimulated production of red blood cells via interaction of erythropoietin with its cellular receptor.
  • In vivo activity of the fusion proteins is tested as follows: Conditioned medium from cells transfected with mEPO/Ig is used to inject mice (B6C3F1 strain, female, Jackson Labs, 18g) . The hematocrits of these mice are measured prior to administering the fusion protein. Approximately 300 U of fusion protein per kg of mouse are injected subcutaneously on day 1, day 3 and day 5. Their hamatocrits are measured on
  • a group of New Zealand white rabbits are injected intravenously with EPO/Ig fusion protein ml in PBS. Blood samples are obtained at 5 minutes and 2, 4, 6, 9, and 24 hours, or at longer time periods, and activity of the circulating erythropoietin fusion protein is measured.

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Abstract

La présente invention concerne la production et l'utilisation de protéines hybrides comprenant des polypeptides d'érythropoïétine et d'immunoglobuline. Ces protéines hybrides d'érythropoïétine présentent une demi-vie augmentée in vivo en comparaison avec l'érythropoïétine de type sauvage. Leur fréquence d'administration aux patients qui en ont besoin est par conséquent réduite par rapport à la fréquence d'administration de l'érythropoïétine naturelle.
PCT/US1998/013930 1997-07-10 1998-07-06 Proteines hybrides recombinees d'erythropoietine / immunoglobuline Ceased WO1999002709A1 (fr)

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WO2001036489A3 (fr) * 1999-11-12 2001-11-08 Merck Patent Gmbh Formes d'erythropoietine dotees de proprietes ameliorees
WO2002079232A3 (fr) * 2001-03-30 2002-12-12 Lexigen Pharm Corp Diminution de l'antigenicite de proteines de fusion
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GB2382580A (en) * 2001-11-29 2003-06-04 Cheil Jedang Corp Erythropoietin- thrombopoietin fusion protein
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US6838260B2 (en) 1997-12-08 2005-01-04 Emd Lexigen Research Center Corp. Heterodimeric fusion proteins useful for targeted immune therapy and general immune stimulation
US6969517B2 (en) 2001-05-03 2005-11-29 Emd Lexigen Research Center Corp. Recombinant tumor specific antibody and use thereof
US7067110B1 (en) 1999-07-21 2006-06-27 Emd Lexigen Research Center Corp. Fc fusion proteins for enhancing the immunogenicity of protein and peptide antigens
US7091321B2 (en) 2000-02-11 2006-08-15 Emd Lexigen Research Center Corp. Enhancing the circulating half-life of antibody-based fusion proteins
US7141651B2 (en) 1999-08-09 2006-11-28 Emd Lexigen Research Center Corp. Multiple cytokine protein complexes
US7148321B2 (en) * 2001-03-07 2006-12-12 Emd Lexigen Research Center Corp. Expression technology for proteins containing a hybrid isotype antibody moiety
US7169904B2 (en) 2002-12-17 2007-01-30 Emd Lexigen Research Center Corp. Immunocytokine sequences and uses thereof
WO2007021129A1 (fr) 2005-08-16 2007-02-22 Hanmi Pharmaceutical Co., Ltd. Procédé pour la production en masse d'une région fc d'immunoglobuline libre de résidus de méthionine initiale
US7186804B2 (en) 2001-12-04 2007-03-06 Emd Lexigen Research Center Corp. IL-2 fusion proteins with modulated selectivity
US7217797B2 (en) 2002-10-15 2007-05-15 Pdl Biopharma, Inc. Alteration of FcRn binding affinities or serum half-lives of antibodies by mutagenesis
US7217798B2 (en) 2003-10-15 2007-05-15 Pdl Biopharma, Inc. Alteration of Fc-fusion protein serum half-lives by mutagenesis
US7265208B2 (en) 2001-05-01 2007-09-04 The Regents Of The University Of California Fusion molecules and treatment of IgE-mediated allergic diseases
US7323549B2 (en) 2003-12-30 2008-01-29 Emd Lexigen Research Center Corp. IL-7 fusion proteins
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US7589179B2 (en) 2004-12-09 2009-09-15 Merck Patent Gmbh IL-7 variants with reduced immunogenicity
US7625564B2 (en) 2006-01-27 2009-12-01 Novagen Holding Corporation Recombinant human EPO-Fc fusion proteins with prolonged half-life and enhanced erythropoietic activity in vivo
US7737260B2 (en) 2003-11-13 2010-06-15 Hanmi Pharm. Co., Ltd Protein complex using an immunoglobulin fragment and method for the preparation thereof
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US6555343B1 (en) 1999-05-07 2003-04-29 Genentech Inc. Chimpanzee erythropoietin (CHEPO) polypeptides and nucleic acids encoding the same
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AU2008217202B2 (en) * 2007-02-22 2014-06-12 Polymun Scientific Immunbiologische Forschung Gmbh Erythropoietin fusion protein
EP1961821A1 (fr) * 2007-02-22 2008-08-27 Polymun Scientific Immunbiologische Forschung GmbH Protéine hybride d'érythropoïétine
WO2008101680A1 (fr) * 2007-02-22 2008-08-28 Polymun Scientific Immunbiologische Forschung Gmbh Protéine de fusion à base d'érythropoïétine
TWI554520B (zh) * 2007-07-20 2016-10-21 諾華健控股公司 在活體中具有延長之半生期以及提高之紅血球生成活性的重組人類紅血球生成素（ｅｐｏ）-ｆｃ融合蛋白
US8067548B2 (en) 2007-07-26 2011-11-29 Novagen Holding Corporation Fusion proteins having mutated immunoglobulin hinge region
US11028398B2 (en) 2007-07-26 2021-06-08 Novagen Holding Corporation Fusion proteins having mutated immunoglobulin hinge region
US8907066B2 (en) 2009-04-22 2014-12-09 Merck Patent Gmbh Antibody fusion proteins with a modified FcRn binding site

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