Recombinant retroviruses expressing a protein that converts a pr

Chemistry: molecular biology and microbiology – Treatment of micro-organisms or enzymes with electrical or... – Modification of viruses

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

435 691, 435372, C12N 508, C12N 510

Patent

active

056911777

ABSTRACT:
Recombinant retroviruses carrying a vector construct capable of preventing, inhibiting, stabilizing or reversing infectious, cancerous or auto-immune diseases are disclosed. More specifically, the recombinant retroviruses of the present invention are useful for (a) stimulating a specific immune response to an antigen or a pathogenic antigen; (b) inhibiting a function of a pathogenic agent, such as a virus; and (c) inhibiting the interaction of an agent with a host cell receptor. In addition, eucaryotic cells infected with, and pharmaceutical compositions containing such a recombinant retrovirus are disclosed. Various methods for producing recombinant retroviruses having unique characteristics, and methods for producing transgenic packaging animals or insects are also disclosed.

REFERENCES:
patent: 4405712 (1983-09-01), Vande Woude et al.
patent: 4650764 (1987-03-01), Temin et al.
patent: 4663281 (1987-05-01), Gillies et al.
patent: 4708818 (1987-11-01), Montagnier et al.
patent: 4725669 (1988-02-01), Essex et al.
patent: 4738922 (1988-04-01), Haseltine et al.
patent: 4861719 (1989-08-01), Miller
patent: 4868116 (1989-09-01), Morgan et al.
patent: 4980286 (1990-12-01), Morgan et al.
patent: 4980289 (1990-12-01), Temin et al.
patent: 5026635 (1991-06-01), Ferguson et al.
patent: 5192553 (1993-03-01), Boyse et al.
patent: 5246924 (1993-09-01), Fox et al.
patent: 5304489 (1994-04-01), Rosen
patent: 5306631 (1994-04-01), Harrison et al.
patent: 5399346 (1995-03-01), Anderson et al.
Nelson et al. "Gene replacment therapy for inborn errors of purine metabolism", Cold Spring Harbor Symp. Quant. Biol., 51(2): 1065-1071, 1986.
Besnard et al., "Selection against expression of the Escherichia coil gene gpt in hprt+ mouse teratocarcinoma and hybrid cells", Mol. Cell, Biol., 7(11): 4139-4141, Nov. 1987.
Borrelli et al., "Targeting of inducible toxic phenotype in animal cells", Proc. Nat. Acad. Sci. USA, 85: 7572-7576, Oct. 1988.
Trucco, "Molecular mechanisms involved in the etiology and pathogenesis of autoimmune diseases", Clin. Investig., 70:756-765, 1992.
Crystal, R. G., "Transfer of Genes to Humans: Early Lessons and Obstacles to Success," Science, 270:404-410 (Oct. 20, 1995).
Barinaga, M., "Step Taken Toward Improved Vectors for Gene Transfer," Science, 266:1326 (Nov. 25, 1994).
Jolly, D., "Viral Vector Systems For Gene Therapy," Cancer Gene Therapy, 1(1):51-64 (1994).
Marshall, E., "Gene Therapy's Growing Pains," Science, 269:1050-1055 (Aug. 25, 1995).
Orkin et al., "Report and Recommendations of the Panel to Assess the NIH Investment in Research on Gene Therapy," (Dec. 7, 1995).
Bachmann, et al., "In Vivo venus In Vitro Assays for Assessment of T-and B-cell Function," Immunological Techniques, 6:320-326 (1994).
Jolly, et al., "Variable Stability of a Selectable Provirus After Retroviral Vector Gene Transfer Into Human Cells," Molecular and Cellular Biology, 6(4):1141-1147 (Apr. 1986).
Willis, et al., "Partial Phenotypic Correction of Human Lesch-Nyhan (Hypoxanthine-Guanine Phosphoribosyltransferase-deficient) Lymphoblasts with a Transmissible Retroviral Vector," The Journal of Biological Chemistry, 259(12):7842-7849 (Jun. 25, 1984).
Klein, G., "Tumor Antigens," Ann. Rev. Microbiol. 20:223-252 (1966).
Hellstrom and Hellstrom, "Cellular Immunity Against Tumor Antigens," Adv. Cancer Res. 12:167-223 (1969).
Bishop, J.M., "Cancer Genes Come Of Age," Cell 32:1018-1020 (1983).
Hellstrom and Hellstrom, "Oncogene-associated Tumor Antigens as Targets for Immunotherapy," FASEB J. 3:1715-1722, (1989).
Miller, et al., "Treatment of B-Cell Lymphoma With Monoclonal Anti-Idiotype Antibody," New England J. Med. 306:517-522, (1982).
Bartram et al., "Translocation of c-abl Oncogene Correlates with the Presence of a Philadelphia Chromosome in chronic Myelocytic Leukaemia," Nature 306:277-280 (1983).
Yasukawa and Zarling, "Human Cytotoxic T Cell Clones Directed Against Herpes Simplex Virus-Infected Cells. III. Analysis of Viral Glycoproteins Recognized by CTL Clones by Using Recombinant Herpes Simplex Viruses," J. lmmunol. 134(4):2679-2682, 1985.
Zarling, et al., "Human Cytotoxic T Cell Clones Directed Against Herpes Simplex Virus-Infected Cells. IV. Recognition and Activation by Cloned Glycoproteins gB and gD," J. lmmunol. 136(12):4669-4673 (1986).
Zarling, et al., "Herpes Simplex Virus (HSV)-Specific Human T-Cell Clones Recognize HSV Glycoprotein D Expressed by a Recombinant Vaccinia Virus," J. Virol. 59(2):506-509 (1986).
Torseth, et al., "Native and Recombinant Herpes Simplex Virus Type 1 Envelope Protein Induce Human Immune T-Lymphocyte Responses," J. Virol. 61(5):1532-1539 (1987).
Kuriyama et al., "Gene therapy for the treatment of hepatoma by retroviral-mediated gene-transfer of the herpes-simplex virus thymidine kinase gene," Int. Hepatol. Commun. 1(5):253-259 (1993).
Kuriyama et al. (b), "A potential approach for gene therapy targeting hepatoma using a liver-specific promoter on a retroviral vector," Cell Struct. Func., 16:503-510 (1991).
Pizer et al., "A mammalian cell line designed to test the mutagenic activity of anti-herpes nucleosides," Int. J. Cancer, 40:114-121 (1987).
Adam et al., "Identification of a Signal in a Murine Retrovirus That Is Sufficient for Packaging of Nonretroviral RNA into Virions," J. Virology, 62(10):3802-3806 (Oct., 1988).
Anderson F.W., "Human Gene Therapy," Science, 256:808-813 (May 8, 1992).
Cone et al., "Regulated Expression of a Complete Human .beta.-Globin Gene Encoded by a Transmissible Retrovirus Vector," Mol. & Cell. Biol, 7(2):887-897 (Feb., 1987).
Cournoyer et al., "Gene Therapy of the Immune System," Ann. Rev. Immunol., 11:297-329 (1993).
Danos et al., "Safe and Efficient Generation of Recombinant Retroviruses With Amphotropic and Ecotropic Host Ranges," Proc. Nat'l Acad. Sci., USA, 85:6460-6464 (Sep., 1988).
Dayton et al., "The Trans-Activator Gene of the Human T Cell Lymphotropic Virus Type III Is Required for Replication," Cell, 44:941-947 (Mar. 28, 1986).
Dzierzak et al., "Lineage-Specific Expression of A Human .beta.-Globin Gene In Murine Bone Marrow Transplant Recipients Reconstituted With Retrovirus-transduced Stem Cells," Nature, 331:35-41 (Jan. 7, 1988).
Felber et al., "A Quantitative Bioassay For HIV-1 Based On Trans-Activation," Science, 239:184-187 (Jan. 8, 1988).
Felgner et al., "Lipofection: A Highly Efficient, Lipid-Mediated DNA-Transfection Procedure," Proc. Nat'l Acad. Sci., USA, 84:7413-7417 (Nov., 1987).
Frankel et al., "Dimerization of the Tat Protein from Human Immunodeficiency Virus: A Cysteine-Rich Peptide Mimics the Normal Metal-Linked Dimer Interface," Proc. Nat'l Acad. Sci., USA, 85:6297-6300 (Sep., 1988).
Frankel et al., "Tat Protein From Human Immunodeficiency Virus Forms A Metal-Linked Dimer," Science, 240:70-73 (Apr., 1988).
Friedman et al., "Expression Of A Truncated Viral Trans-Activator Selectively Impedes Lyric Infection By Its Cognate Virus," Nature, 335:452-454 (Sep. 29, 1988).
Furman et al., "Inhibition of Herpes Simplex Virus-Induced DNA Polymerase Activity and Vital DNA Replication by 9-(2-Hydroxyethoxymethyl)guanine and Its Triphosphate," J. Virology, 32(1):72-77 (Oct., 1979).
Ganz et al., "Defensins Natural Peptide Antibiotics of Human Neutrophils," J. Clin. Invest., 76:1427-1435 (Oct., 1985).
Goelz, S.E., "Hypomethylation of DNA from Benign and Malignant Human Colon Neoplasms," Science, 228:187-190 (Apr. 12, 1985).
Graham et al., "A New Technique for the Assay of Infectivity of Human Adenovirus 5 DNA," J. Virology, 52:456-467 (1973).
Guild et al., "Development of Retrovirus Vectors Useful for Expressing Genes in Cultured Murine Embryonal Cells and Hematopoietic Cells In Vivo," J. Virol., 62(10):3795-3801 (1988).
Hirsch, M.S., "Aids Commentary: Azidothymidine," J. Infect. Dis., 157(3):427-431 (1988).
Ho et al., "A T-Cell-Specific Transcriptional Enhancer Element 3' of C.sub..alpha. in the Human T-Cell Receptor a Locus," Proc. Nat'l Acad. Sci., USA, 86:6714-6718 (Sep., 1989).
Kantoff et al., "Correction of Adenosine Dearninase Deficiency in Cultured Human T and B Cells by Retrovirus-mediated Gene Transfer," Proc. N

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Recombinant retroviruses expressing a protein that converts a pr does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Recombinant retroviruses expressing a protein that converts a pr, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Recombinant retroviruses expressing a protein that converts a pr will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2106011

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.