逆转录酶
抗药性
人类免疫缺陷病毒(HIV)
抗性突变
药品
病毒学
抗性(生态学)
化学
艾滋病毒耐药性
药理学
生物
遗传学
抗逆转录病毒疗法
病毒载量
核糖核酸
基因
生态学
作者
Maria E. Cilento,Karen A. Kirby,Stefan G. Sarafianos
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2021-01-28
卷期号:121 (6): 3271-3296
被引量:41
标识
DOI:10.1021/acs.chemrev.0c00967
摘要
HIV reverse transcriptase (RT) is an enzyme that plays a major role in the replication cycle of HIV and has been a key target of anti-HIV drug development efforts. Because of the high genetic diversity of the virus, mutations in RT can impart resistance to various RT inhibitors. As the prevalence of drug resistance mutations is on the rise, it is necessary to design strategies that will lead to drugs less susceptible to resistance. Here we provide an in-depth review of HIV reverse transcriptase, current RT inhibitors, novel RT inhibitors, and mechanisms of drug resistance. We also present novel strategies that can be useful to overcome RT's ability to escape therapies through drug resistance. While resistance may not be completely avoidable, designing drugs based on the strategies and principles discussed in this review could decrease the prevalence of drug resistance.
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