Relationships among various nucleoside resistance-conferring mutations in the reverse transcriptase of HIV-1

被引:14
|
作者
Turner, D [1 ]
Brenner, B [1 ]
Wainberg, MA [1 ]
机构
[1] McGill Univ, Jewish Gen Hosp, AIDS Ctr, Lady Davis Inst, Montreal, PQ H3T 1E2, Canada
基金
加拿大健康研究院;
关键词
HIV; NRTIs; resistance; mutations; antiretroviral drugs; nucleosides; diminished sensitivity; viral fitness;
D O I
10.1093/jac/dkh009
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Highly active antiretroviral therapy has significantly improved HIV-related morbidity and mortality, and nucleoside reverse transcriptase inhibitors remain an essential component of treatment. However, the emergence of HIV-1 mutated strains that are resistant to one or more antiretroviral drugs is a leading cause of treatment failure among patients living with HIV/AIDS. These resistant strains may often suffer from a replication disadvantage in comparison with wild-type viruses when grown in the absence of drug pressure and a potential benefit in this regard has been shown for lamivudine-resistant viruses that contain a M184V mutation in reverse transcriptase, as well as for several other drug-resistant viral variants. Interactions between different mutations may complicate the understanding of HIV drug resistance with regard to the likelihood of therapeutic success.
引用
收藏
页码:53 / 57
页数:5
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