Requirements for efficient production and transduction of human immunodeficiency virus type 1-based vectors.

Abstract:

:A number of human immunodeficiency type 1 (HIV-1)-based vectors have recently been shown to transduce nondividing cells in vivo as well as in vitro. However, if these vectors are to be considered for eventual clinical use, a major consideration is to reduce the probability of unintended generation of replication-competent virus. This can be achieved by eliminating viral genetic elements involved in the generation of replication-competent virus without impairing vector production. We have designed a system to transiently produce HIV-1-based vectors by using expression plasmids encoding Gag, Pol, and Tat of HIV-1 under the control of the cytomegalovirus immediate-early promoter. Our data show that the best vector yield is achieved in the presence of the Rev/Rev-responsive element (RRE) system. However, the constitutive transport element of Mason-Pfizer monkey virus can substitute for RRE and Rev at least to some extent, whereas the posttranscriptional regulatory element of human hepatitis B virus appeared to be inefficient. In addition, we show that high-titer virus preparations can be obtained in the presence of sodium butyrate, which activates the expression of both the packaging construct and the vector genome. Finally, our results suggest that efficient infectivity of vectors defective in the accessory proteins Vif, Vpr, Vpu, and Nef depends on the nature of the target cells.

journal_name

J Virol

journal_title

Journal of virology

authors

Gasmi M,Glynn J,Jin MJ,Jolly DJ,Yee JK,Chen ST

doi

10.1128/JVI.73.3.1828-1834.1999

subject

Has Abstract

pub_date

1999-03-01 00:00:00

pages

1828-34

issue

3

eissn

0022-538X

issn

1098-5514

journal_volume

73

pub_type

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