Mechanisms of inhibition of HIV replication by non-nucleoside reverse transcriptase inhibitors

被引:123
|
作者
Sluis-Cremer, Nicolas [1 ]
Tachedjian, Gilda [2 ,3 ,4 ]
机构
[1] Univ Pittsburgh, Sch Med, Div Infect Dis, Pittsburgh, PA 15261 USA
[2] Macfarlane Burnet Inst Med Res & Publ Hlth, Mol Interact Grp, Melbourne, Vic 3004, Australia
[3] Monash Univ, Dept Microbiol, Clayton, Vic 3168, Australia
[4] Monash Univ, Dept Med, Prahran, Vic 3181, Australia
关键词
HIV; reverse transcriptase; non-nucleoside; Gag-Pol; viral entry;
D O I
10.1016/j.virusres.2008.01.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The non-nucleoside reverse transcriptase (RT) inhibitors (NNRTIs) are a therapeutic class of compounds that are routinely used, in combination with other antiretroviral drugs, to treat HIV-1 infection. NNRTIs primarily block HIV-1 replication by preventing RT from completing reverse transcription of the viral single-stranded RNA genome into DNA. However, some NNRTIs, such as efavirenz, have been shown to inhibit the late stages of HIV-1 replication by interfering with HIV-1 Gag-Pol polyprotein processing, while others, such as the pyrimidinediones, have been shown to inhibit both HIV-1 RT-mediated reverse transcription and HIV-1/HIV-2 viral entry. Accordingly, in this review we describe the multiple mechanisms by which NNRTIs inhibit HIV-1 reverse transcription (and in some cases HIV-2 reverse transcription) and other key steps involved in HIV-1/HIV-2 replication. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:147 / 156
页数:10
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