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Minimal requirement for a lentivirus vector based on human immunodeficiency virus type 1.


ABSTRACT: The use of human immunodeficiency virus vectors for gene therapy is hampered by concern over their safety. This concern might be ameliorated, in part, if the viral accessory genes and proteins could be eliminated from the vector genomes and particles. Here we describe a minimal vector system that is capable of transducing nondividing cells and which does not contain tat, vif, vpr, vpu, and nef.

SUBMITTER: Kim VN 

PROVIDER: S-EPMC109441 | biostudies-literature | 1998 Jan

REPOSITORIES: biostudies-literature

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Minimal requirement for a lentivirus vector based on human immunodeficiency virus type 1.

Kim V N VN   Mitrophanous K K   Kingsman S M SM   Kingsman A J AJ  

Journal of virology 19980101 1


The use of human immunodeficiency virus vectors for gene therapy is hampered by concern over their safety. This concern might be ameliorated, in part, if the viral accessory genes and proteins could be eliminated from the vector genomes and particles. Here we describe a minimal vector system that is capable of transducing nondividing cells and which does not contain tat, vif, vpr, vpu, and nef. ...[more]

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