Retroviral vectors

The majority of clinical trials for gene therapy currently employ retroviral-mediated gene delivery. This is because the life cycle of the retrovirus is well understood and can be effectively manipulated to generate vectors that can be efficiently and safely packaged. Here, we review the molecular technology behind the generation of recombinant retroviral vectors. We also highlight the problems associated with the use of these viruses as gene therapy vehicles and discuss future developments that will be necessary to maintain retroviral vectors at the forefront of gene transfer technology.

[1]  A. Rein,et al.  Basis for receptor specificity of nonecotropic murine leukemia virus surface glycoprotein gp70SU , 1992, Journal of virology.

[2]  A. Miller Retrovirus packaging cells. , 1990, Human gene therapy.

[3]  A. Miller,et al.  Non–invasive liposome–mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice , 1993 .

[4]  D. Kabat,et al.  Overcoming interference to retroviral superinfection results in amplified expression and transmission of cloned genes. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[5]  Richard A. Morgan,et al.  Gene Therapy for Infectious Diseases , 1998, Clinical Microbiology Reviews.

[6]  W F Anderson,et al.  Gene therapy for the treatment of brain tumors using intra-tumoral transduction with the thymidine kinase gene and intravenous ganciclovir. , 1993, Human gene therapy.

[7]  S. Russell,et al.  Gene transfer technologies for the gene therapy of cancer. , 1994, Gene therapy.

[8]  D. Littman,et al.  Packaging system for rapid production of murine leukemia virus vectors with variable tropism , 1992, Journal of virology.

[9]  K. Cornetta,et al.  Analysis of retroviral packaging lines for generation of replication-competent virus. , 1990, Virology.

[10]  F. Cosset,et al.  Packaging cells for avian leukosis virus-based vectors with various host ranges , 1992, Journal of virology.

[11]  D. Cosman,et al.  Stably transmitted triple-promoter retroviral vectors and their use in transformation of primary mammalian cells , 1988, Molecular and cellular biology.

[12]  R. Vile,et al.  Identification of a generalised packaging sequence for D-type retroviruses and generation of a D-type retroviral vector. , 1992, Virology.

[13]  C. Southam DIVISION OF MICROBIOLOGY: PRESENT STATUS OF ONCOLYTIC VIRUS STUDIES* , 1960 .

[14]  J. Roth,et al.  A retroviral wild-type p53 expression vector penetrates human lung cancer spheroids and inhibits growth by inducing apoptosis. , 1993, Cancer research.

[15]  F. Jensen,et al.  Human serum lyses RNA tumour viruses , 1975, Nature.

[16]  W. Anderson,et al.  Analysis of the functional and host range-determining regions of the murine ectropic and amphotropic retrovirus envelope proteins , 1993, Journal of virology.

[17]  A. Miller,et al.  Human gene therapy comes of age , 1992, Nature.

[18]  M. Emerman,et al.  A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells , 1993, Nature.

[19]  S. Russell Replicating vectors for cancer therapy: a question of strategy. , 1994, Seminars in cancer biology.

[20]  A. Panganiban,et al.  Ordered interstrand and intrastrand DNA transfer during reverse transcription. , 1988, Science.

[21]  F. Collins,et al.  Cystic fibrosis: molecular biology and therapeutic implications. , 1992, Science.

[22]  M. Hatzoglou,et al.  Hormonal control of interacting promoters introduced into cells by retroviruses. , 1991, The Journal of biological chemistry.

[23]  R. Ramesh,et al.  Biology of disease: The biology of cancer gene therapy , 1995 .

[24]  K. Cornetta,et al.  No retroviremia or pathology in long-term follow-up of monkeys exposed to a murine amphotropic retrovirus. , 1991, Human gene therapy.

[25]  Melchner,et al.  Identification of cellular promoters by using a retrovirus promoter trap , 1989, Journal of virology.

[26]  K. Cornetta,et al.  Amphotropic murine leukemia retrovirus is not an acute pathogen for primates. , 1990, Human gene therapy.

[27]  A. Wynshaw-Boris,et al.  Hepatic gene transfer in animals using retroviruses containing the promoter from the gene for phosphoenolpyruvate carboxykinase. , 1990, The Journal of biological chemistry.

[28]  J. Stephenson Molecular biology of RNA tumor viruses , 1980 .

[29]  M. Nicolson,et al.  Replication-defective chimeric helper proviruses and factors affecting generation of competent virus: expression of Moloney murine leukemia virus structural genes via the metallothionein promoter , 1987, Molecular and cellular biology.

[30]  D. Baltimore,et al.  Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus , 1983, Cell.

[31]  E. Jaffee,et al.  Vaccination with irradiated tumor cells engineered to secrete murine granulocyte-macrophage colony-stimulating factor stimulates potent, specific, and long-lasting anti-tumor immunity. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[32]  H. Temin,et al.  The terminal nucleotides of retrovirus DNA are required for integration but not virus production , 1983, Nature.

[33]  R. Mulligan,et al.  The basic science of gene therapy. , 1993, Science.

[34]  S. Hughes,et al.  Appropriate in vivo expression of a muscle-specific promoter by using avian retroviral vectors for gene transfer [corrected] , 1992, Journal of virology.

[35]  T. Friedmann Gene therapy of cancer through restoration of tumor‐suppressor functions? , 1992, Cancer.

[36]  C. Cepko,et al.  Lineage analysis in the vertebrate nervous system by retrovirus-mediated gene transfer. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[37]  R. Mulligan,et al.  Safe and efficient generation of recombinant retroviruses with amphotropic and ecotropic host ranges. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[38]  B. Sullenger,et al.  Improved gene expression upon transfer of the adenosine deaminase minigene outside the transcriptional unit of a retroviral vector. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[39]  H. Temin,et al.  New retrovirus helper cells with almost no nucleotide sequence homology to retrovirus vectors , 1989, Journal of virology.

[40]  S. Eccles,et al.  Decreased tumorigenicity of a transplantable rat sarcoma following transfer and expression of an IL‐2 cDNA , 1991, International journal of cancer.

[41]  O. Danos,et al.  Receptor choice determinants in the envelope glycoproteins of amphotropic, xenotropic, and polytropic murine leukemia viruses , 1992, Journal of virology.

[42]  R. Kerbel,et al.  Retroviral insertional mutagenesis as a strategy for the identification of genes associated with cis-diamminedichloroplatinum(II) resistance. , 1995, Cancer research.

[43]  R. Martuza,et al.  Gene therapy of maliganant brain tumors: A rat glioma line bearing the herpes simplex virus type 1‐thymidine kinase gene and wild type retrovirus kills other tumor cells , 1992, Journal of neuroscience research.

[44]  R. Scharfmann,et al.  Long-term in vivo expression of retrovirus-mediated gene transfer in mouse fibroblast implants. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[45]  S. Russell,et al.  Immunity to B16 melanoma in mice immunized with IL‐2‐secreting allogeneic mouse fibroblasts expressing melanoma‐associated antigens , 1992, International journal of cancer.

[46]  H. Temin,et al.  High mutation rate of a spleen necrosis virus-based retrovirus vector , 1986, Molecular and cellular biology.

[47]  S. Russell Gene therapy for cancer , 1992, The Lancet.

[48]  Z. Ram,et al.  Toxicity studies of retroviral-mediated gene transfer for the treatment of brain tumors. , 1993, Journal of neurosurgery.

[49]  E. Gilboa,et al.  Gene therapy for infectious diseases: the AIDS model. , 1994, Trends in genetics : TIG.

[50]  R. Weiss Cellular Receptors and Viral Glycoproteins Involved in Retrovirus Entry , 1993 .

[51]  M. Roth,et al.  A chimeric avian retrovirus containing the influenza virus hemagglutinin gene has an expanded host range , 1992, Journal of virology.

[52]  G. Winter,et al.  Retroviral vectors displaying functional antibody fragments. , 1993, Nucleic acids research.

[53]  T. Asada Treatment of human cancer with mumps virus , 1974, Cancer.

[54]  W. F. Anderson What about those monkeys that got T-cell lymphoma? , 1993, Human gene therapy.

[55]  J. Roth,et al.  Prevention of orthotopic human lung cancer growth by intratracheal instillation of a retroviral antisense K-ras construct. , 1993, Cancer research.

[56]  Y Takeuchi,et al.  Type C retrovirus inactivation by human complement is determined by both the viral genome and the producer cell , 1994, Journal of virology.

[57]  T Friedmann,et al.  Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[58]  M. Raffeld,et al.  Helper virus induced T cell lymphoma in nonhuman primates after retroviral mediated gene transfer , 1992, The Journal of experimental medicine.

[59]  M. Emerman,et al.  Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus , 1994, Journal of virology.

[60]  J. Brookfield,et al.  Neutralism and selectionism face up to DNA data. , 1994, Trends in genetics : TIG.

[61]  R. Vile Selectable markers for eukaryotic cells. , 1992, Methods in molecular biology.

[62]  Y. Ron,et al.  A spleen necrosis virus-based retroviral vector which expresses two genes from a dicistronic mRNA. , 1992, Virology.

[63]  R. Vile,et al.  A comparison of the properties of different retroviral vectors containing the murine tyrosinase promoter to achieve transcriptionally targeted expression of the HSVtk or IL-2 genes. , 1994, Gene therapy.

[64]  C. Richards,et al.  Retroviral-mediated gene therapy for the treatment of hepatocellular carcinoma: an innovative approach for cancer therapy. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[65]  S. Hughes,et al.  Retroviral reverse transcription and integration: progress and problems. , 1992, Annual review of cell biology.

[66]  A. Miller,et al.  Internal initiation of translation in retroviral vectors carrying picornavirus 5' nontranslated regions , 1991, Journal of virology.

[67]  R. Edwards,et al.  Cloning of the cellular receptor for amphotropic murine retroviruses reveals homology to that for gibbon ape leukemia virus. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[68]  N. Dillon Regulating gene expression in gene therapy. , 1993, Trends in biotechnology.

[69]  J. Roth,et al.  Therapeutic effect of a retroviral wild-type p53 expression vector in an orthotopic lung cancer model. , 1994, Journal of the National Cancer Institute.

[70]  D. Pennington,et al.  Specific ablation of human immunodeficiency virus Tat-expressing cells by conditionally toxic retroviruses. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[71]  M. Bender,et al.  Evidence that the packaging signal of Moloney murine leukemia virus extends into the gag region , 1987, Journal of virology.

[72]  A. Miller,et al.  Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production , 1986, Molecular and cellular biology.

[73]  S. Goff,et al.  A safe packaging line for gene transfer: separating viral genes on two different plasmids , 1988, Journal of virology.

[74]  A. Davison,et al.  Molecular virology: a practical approach , 1993 .

[75]  E. Gilboa,et al.  A pilot study of immunization with HLA-A2 matched allogeneic melanoma cells that secrete interleukin-2 in patients with metastatic melanoma. , 1992, Human gene therapy.

[76]  H. Temin,et al.  Recent advances in retrovirus vector technology. , 1993, Current opinion in genetics & development.

[77]  O. Elroy-Stein,et al.  Retroviral vectors containing putative internal ribosome entry sites: development of a polycistronic gene transfer system and applications to human gene therapy. , 1992, Nucleic acids research.

[78]  K. Cornetta,et al.  Gene transfer into humans--immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction. , 1990, The New England journal of medicine.

[79]  A. Miller,et al.  Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection , 1990, Molecular and cellular biology.

[80]  K. Sikora,et al.  Gene therapy for cancer using tumour-specific prodrug activation. , 1994, Gene therapy.

[81]  T. Palmer,et al.  Genetically modified skin fibroblasts persist long after transplantation but gradually inactivate introduced genes. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[82]  A. Chang,et al.  Immunotherapy of malignancy by in vivo gene transfer into tumors. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[83]  D. Housman,et al.  A new retrovirus packaging cell for gene transfer constructed from amplified long terminal repeat-free chimeric proviral genes , 1992, Journal of virology.

[84]  J. Yee,et al.  Gene expression from transcriptionally disabled retroviral vectors. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[85]  M. Emerman,et al.  Genes with promoters in retrovirus vectors can be independently suppressed by an epigenetic mechanism , 1984, Cell.

[86]  R. Vile,et al.  Targeted vectors for gene therapy , 1995, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[87]  C. Richards,et al.  Generation of a transgenic model for retrovirus-mediated gene therapy for hepatocellular carcinoma is thwarted by the lack of transgene expression. , 1993, Human gene therapy.

[88]  Z. Ram,et al.  In situ retroviral-mediated gene transfer for the treatment of brain tumors in rats. , 1993, Cancer research.

[89]  H. Land,et al.  Advanced mammalian gene transfer: high titre retroviral vectors with multiple drug selection markers and a complementary helper-free packaging cell line. , 1990, Nucleic acids research.

[90]  Z. Ram,et al.  In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. , 1992, Science.

[91]  F. Marshall,et al.  High efficiency gene transfer into primary human tumor explants without cell selection. , 1993, Cancer research.

[92]  C. Higgins,et al.  Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy , 1993, Nature.

[93]  T. Dupressoir,et al.  Inhibition by parvovirus H-1 of the formation of tumors in nude mice and colonies in vitro by transformed human mammary epithelial cells. , 1989, Cancer research.

[94]  A. Panganiban,et al.  Human immunodeficiency virus vectors for inducible expression of foreign genes , 1992, Journal of virology.

[95]  S. Carillo,et al.  The efficiency of cell targeting by recombinant retroviruses depends on the nature of the receptor and the composition of the artificial cell-virus linker. , 1992, The Journal of general virology.

[96]  H. Varmus,et al.  Efficient incorporation of human CD4 protein into avian leukosis virus particles. , 1990, Science.

[97]  S. Rosenberg,et al.  The Development of Gene Therapy for the Treatment of Cancer , 1993, Annals of surgery.

[98]  R. Vile,et al.  Retroviruses as vectors. , 1995, British medical bulletin.

[99]  K. Cornetta SAFETY ASPECTS OF GENE THERAPY , 1992, British journal of haematology.

[100]  P. Bruggen,et al.  Molecular definition of tumor antigens recognized by T lymphocytes. , 1992 .

[101]  J. Cunningham,et al.  Human cells infected with retrovirus vectors acquire an endogenous murine provirus , 1990, Journal of virology.

[102]  Flügel Rm Spumaviruses: a group of complex retroviruses. , 1991 .

[103]  R. Mulligan,et al.  Lineage-specific expression of a human β-globin gene in murine bone marrow transplant recipients reconstituted with retrovirus-transduced stem cells , 1988, Nature.

[104]  L. Cupples,et al.  A model for predicting the risk of cancer consequent to retroviral gene therapy. , 1992, Human gene therapy.

[105]  K. Harbers,et al.  Retroviral integration sites in transgenic Mov mice frequently map in the vicinity of transcribed DNA regions , 1990, Journal of virology.

[106]  Philippe Soriano,et al.  Promoter interactions in retrovirus vectors introduced into fibroblasts and embryonic stem cells , 1991, Journal of virology.

[107]  J. Coffin,et al.  Highly preferred targets for retrovirus integration , 1988, Cell.

[108]  Brian Salmons,et al.  Targeting of retroviral vectors for gene therapy. , 1993, Human gene therapy.

[109]  Joseph Zabner,et al.  Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis , 1993, Cell.

[110]  Y. Ron,et al.  High rate of genetic rearrangement during replication of a Moloney murine leukemia virus-based vector , 1993, Journal of virology.

[111]  E. Gilboa,et al.  Comparison of the expression of a mutant dihydrofolate reductase under control of different internal promoters in retroviral vectors. , 1992, Human gene therapy.