Cheng et al., 2005 - Google Patents
Efficient gene transfer to retinal pigment epithelium cells with long-term expressionCheng et al., 2005
View PDF- Document ID
- 13188138117008757468
- Author
- Cheng L
- Toyoguchi M
- Looney D
- Lee J
- Davidson M
- Freeman W
- Publication year
- Publication venue
- Retina
External Links
Snippet
Purpose: To evaluate the safety and efficiency of feline immunodeficiency virus (FIV) vectors for gene delivery into the mammalian retina. Methods: A first-generation FIV vector was constructed and administered into rabbit eyes at two different concentrations by intravitreal …
- 210000003583 Retinal Pigment Epithelium 0 title abstract description 41
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/162—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from virus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICRO-ORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING OR MAINTAINING MICRO-ORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
- C12N15/86—Viral vectors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICRO-ORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING OR MAINTAINING MICRO-ORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2740/00—Reverse Transcribing RNA Viruses
- C12N2740/00011—Reverse Transcribing RNA Viruses
- C12N2740/10011—Retroviridae
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Balaggan et al. | Stable and efficient intraocular gene transfer using pseudotyped EIAV lentiviral vectors | |
| Boye et al. | The human rhodopsin kinase promoter in an AAV5 vector confers rod-and cone-specific expression in the primate retina | |
| Bainbridge et al. | In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium | |
| Grant et al. | Evaluation of recombinant adeno-associated virus as a gene transfer vector for the retina | |
| Krishnan et al. | Overexpression of soluble Fas ligand following adeno-associated virus gene therapy prevents retinal ganglion cell death in chronic and acute murine models of glaucoma | |
| Ivanova et al. | Evaluation of AAV-mediated expression of Chop2-GFP in the marmoset retina | |
| Colella et al. | Ocular gene therapy: current progress and future prospects | |
| Reid et al. | Improvement of photoreceptor targeting via intravitreal delivery in mouse and human retina using combinatory rAAV2 capsid mutant vectors | |
| US20130323302A1 (en) | Treatment of amd using aav sflt-1 | |
| Hauswirth et al. | Ocular gene therapy: quo vadis? | |
| JP2025131592A (en) | Treating retinitis pigmentosa using engineered meganucleases | |
| US20210388387A1 (en) | Synp151 (proc29), a promoter for the specific expression of genes in retinal ganglion cells | |
| Cheng et al. | Efficient gene transfer to retinal pigment epithelium cells with long-term expression | |
| Xu et al. | Subretinal delivery of AAV2-mediated human erythropoietin gene is protective and safe in experimental diabetic retinopathy | |
| Nickells et al. | AAV2-mediated transduction of the mouse retina after optic nerve injury | |
| Kong et al. | Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse | |
| Igarashi et al. | Tyrosine triple mutated AAV2-BDNF gene therapy in a rat model of transient IOP elevation | |
| US11981911B2 (en) | Compositions and methods for inhibiting viral vector-induced inflammatory responses | |
| Surace et al. | Delivery of adeno-associated virus vectors to the fetal retina: impact of viral capsid proteins on retinal neuronal progenitor transduction | |
| Bemelmans et al. | Retinal cell type expression specificity of HIV‐1‐derived gene transfer vectors upon subretinal injection in the adult rat: influence of pseudotyping and promoter | |
| Chambers et al. | Lipid nanoparticle-mediated delivery of mRNA into the mouse and human retina and other ocular tissues | |
| Öner | Recent advancements in gene therapy for hereditary retinal dystrophies | |
| Kreppel et al. | Long-term transgene expression in the RPE after gene transfer with a high-capacity adenoviral vector | |
| Loewen et al. | Comparison of wild‐type and class I integrase mutant‐FIV vectors in retina demonstrates sustained expression of integrated transgenes in retinal pigment epithelium | |
| US20250170276A1 (en) | Gene delivery vector for delivering human vegf receptor fusion protein and use thereof |