Expression in Progeny Cells Mosaicism and Heterogeneous Gene Integration and Results in Transduction Compromised by a Delay in Proviral Hematopoietic Progenitor Cells Is Lentivirus Gene Transfer in Murine

10.1128/JVI.74.24.11911-11918.2000. 2000, 74(24):11911. DOI: J. Virol. Didier Trono and Stefan Karlsson Hildur Helgadottir, Isao Hamaguchi, Sten-Eirik Jacobsen, Hanna Mikkola, Niels-Bjarne Woods, Marketa Sjögren, Expression in Progeny Cells Mosaicism and Heterogeneous Gene Integration and Results in Transduction Compromised by a Delay in Proviral Hematopoietic Progenitor Cells Is Lentivirus Gene Transfer in Murine

[1]  Luc Montagnier,et al.  HIV-1 Genome Nuclear Import Is Mediated by a Central DNA Flap , 2000, Cell.

[2]  X. Wang,et al.  Efficient and sustained transgene expression in human corneal cells mediated by a lentiviral vector , 2000, Gene Therapy.

[3]  J. Bloch,et al.  Lentiviral Gene Transfer to the Nonhuman Primate Brain , 1999, Experimental Neurology.

[4]  P. Robbins,et al.  Infection of intact human islets by a lentiviral vector , 1999, Gene Therapy.

[5]  Y. Korin,et al.  Nonproductive Human Immunodeficiency Virus Type 1 Infection in Nucleoside-Treated G0 Lymphocytes , 1999, Journal of Virology.

[6]  L. Naldini,et al.  Interaction of Human Immunodeficiency Virus-Derived Vectors with Wild-Type Virus in Transduced Cells , 1999, Journal of Virology.

[7]  D. Trono,et al.  Transgene expression in the guinea pig cochlea mediated by a lentivirus-derived gene transfer vector. , 1999, Human gene therapy.

[8]  J. Garcia,et al.  Human cord blood CD34+CD38- cell transduction via lentivirus-based gene transfer vectors. , 1999, Human gene therapy.

[9]  P. Brown,et al.  Transduction of Human Progenitor Hematopoietic Stem Cells by Human Immunodeficiency Virus Type 1-Based Vectors Is Cell Cycle Dependent , 1999, Journal of Virology.

[10]  J. Garcia,et al.  Efficient transduction of human lymphocytes and CD34+ cells via human immunodeficiency virus-based gene transfer vectors. , 1999, Human gene therapy.

[11]  T. Hope,et al.  Woodchuck Hepatitis Virus Posttranscriptional Regulatory Element Enhances Expression of Transgenes Delivered by Retroviral Vectors , 1999, Journal of Virology.

[12]  L. Naldini,et al.  Stable transduction of quiescent CD34(+)CD38(-) human hematopoietic cells by HIV-1-based lentiviral vectors. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[13]  B. Torbett,et al.  Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors. , 1999, Science.

[14]  D. Trono,et al.  Self-Inactivating Lentivirus Vector for Safe and Efficient In Vivo Gene Delivery , 1998, Journal of Virology.

[15]  D. Trono,et al.  A Third-Generation Lentivirus Vector with a Conditional Packaging System , 1998, Journal of Virology.

[16]  V. Pathak,et al.  Deoxyribonucleoside Triphosphate Pool Imbalances In Vivo Are Associated with an Increased Retroviral Mutation Rate , 1998, Journal of Virology.

[17]  Fred H. Gage,et al.  Development of a Self-Inactivating Lentivirus Vector , 1998, Journal of Virology.

[18]  I. Weissman,et al.  HIV, but not murine leukemia virus, vectors mediate high efficiency gene transfer into freshly isolated G0/G1 human hematopoietic stem cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[19]  P. Brown,et al.  Human Immunodeficiency Virus Type 1 Vectors Efficiently Transduce Human Hematopoietic Stem Cells , 1998, Journal of Virology.

[20]  Y. Korin,et al.  Progression to the G1b Phase of the Cell Cycle Is Required for Completion of Human Immunodeficiency Virus Type 1 Reverse Transcription in T Cells , 1998, Journal of Virology.

[21]  T. Shimada,et al.  Stable integration of human immunodeficiency virus-based retroviral vectors into the chromosomes of nondividing cells. , 1998, Human gene therapy.

[22]  D. Peterson,et al.  Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors , 1997, Nature Genetics.

[23]  L. Cheng,et al.  A GFP reporter system to assess gene transfer and expression in human hematopoietic progenitor cells , 1997, Gene Therapy.

[24]  F. Gage,et al.  Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[25]  Luigi Naldini,et al.  Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo , 1997, Nature Biotechnology.

[26]  S. Karlsson,et al.  Viral vectors for gene therapy of hematopoietic cells. , 1997, Immunotechnology : an international journal of immunological engineering.

[27]  S. Karlsson,et al.  Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[28]  R. Mulligan,et al.  A stable human-derived packaging cell line for production of high titer retrovirus/vesicular stomatitis virus G pseudotypes. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[29]  Linzhao Cheng,et al.  Use of green fluorescent protein variants to monitor gene transfer and expression in mammalian cells , 1996, Nature Biotechnology.

[30]  F. Gage,et al.  In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral Vector , 1996, Science.

[31]  I. Chen,et al.  High-efficiency gene transfer into CD34+ cells with a human immunodeficiency virus type 1-based retroviral vector pseudotyped with vesicular stomatitis virus envelope glycoprotein G , 1996, Journal of virology.

[32]  R. Pomerantz,et al.  Increasing transduction efficiency of recombinant murine retrovirus vectors by initiation of endogenous reverse transcription: potential utility for genetic therapies , 1995, Journal of virology.

[33]  M. Chalfie,et al.  Green fluorescent protein as a marker for gene expression. , 1994, Science.

[34]  A. Meyerhans,et al.  Restriction and enhancement of human immunodeficiency virus type 1 replication by modulation of intracellular deoxynucleoside triphosphate pools , 1994, Journal of virology.

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

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

[37]  F. Lori,et al.  Low levels of deoxynucleotides in peripheral blood lymphocytes: a strategy to inhibit human immunodeficiency virus type 1 replication. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[38]  M. J. Cormier,et al.  Primary structure of the Aequorea victoria green-fluorescent protein. , 1992, Gene.

[39]  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.

[40]  M. Stevenson,et al.  HIV‐1 replication is controlled at the level of T cell activation and proviral integration. , 1990, The EMBO journal.

[41]  P. Mastromarino,et al.  Characterization of membrane components of the erythrocyte involved in vesicular stomatitis virus attachment and fusion at acidic pH. , 1987, The Journal of general virology.

[42]  M. Kay,et al.  Efficient lentiviral transduction of liver requires cell cycling in vivo , 2000, Nature Genetics.

[43]  Y. Arsenijévic,et al.  Self-inactivating lentiviral vectors with enhanced transgene expression as potential gene transfer system in Parkinson's disease. , 2000, Human gene therapy.

[44]  I. Verma,et al.  3 Lentiviral Vectors , 1999 .

[45]  S. Karlsson,et al.  Retroviral vector design for long-term expression in murine hematopoietic cells in vivo. , 1994, Blood.