Mechanism of HIV antiretroviral drugs progress toward drug resistance

被引:30
|
作者
Ammaranond, Palanee [1 ]
Sanguansittianan, Sayompoo [1 ]
机构
[1] Chulalongkorn Univ, Dept Transfus Med, Fac Allied Hlth Sci, Innovat Ctr Res & Dev Med Diagnost Technol Projec, Bangkok 10330, Thailand
关键词
antiretroviral; drug resistance; HIV; HUMAN-IMMUNODEFICIENCY-VIRUS; TYPE-1; REVERSE-TRANSCRIPTASE; SOCIETY-USA PANEL; TREATMENT EXPERIENCED PATIENTS; PROTEASE INHIBITOR RESISTANCE; RIBONUCLEASE-H ACTIVITY; ACID MUTATION PATTERNS; CROSS-RESISTANCE; BASE-LINE; COMBINATION THERAPY;
D O I
10.1111/j.1472-8206.2011.01009.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The rapid replication rate of HIV-1 RNA and its inherent genetic variation have led to the production of many HIV-1 variants with decreased drug susceptibility. The capacity of HIV to develop drug resistance mutations is a major obstacle to long-term effective anti-HIV therapy. Incomplete suppression of viral replication with an initial drug regimen diminishes the clinical benefit to the patient and may promote the development of broader drug resistance that may cause subsequent treatment regimens to be ineffective. The increased clinical use of combination antiretroviral treatment for HIV-1 infection has led to the selection of viral strains resistant to multiple drugs, including strains resistant to all licensed nucleoside analog RT inhibitors and protease inhibitors. Therefore, it is important to understand the influence of such mutations on viral properties such as replicative fitness, fidelity, and mutation rates. Although research continues to improve our understanding of resistance, leading to refined treatment strategies and, in some cases, improved outcome, resistance to antiretroviral therapy remains a major cause of treatment failure among patients living with HIV-1.
引用
收藏
页码:146 / 161
页数:16
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