Small-molecule HIV-1 entry inhibitors targeting the epitopes of broadly neutralizing antibodies

表位 抗体 人类免疫缺陷病毒(HIV) 病毒学 免疫学 中和抗体 小分子 生物 遗传学
作者
Shibo Jiang,Alexander V. Tuzikov,Alexander M. Andrianov
出处
期刊:Cell chemical biology [Elsevier BV]
卷期号:29 (5): 757-773 被引量:6
标识
DOI:10.1016/j.chembiol.2022.03.009
摘要

Summary

Highly active antiretroviral therapy currently used for HIV/AIDS has significantly increased the life expectancy of HIV-infected individuals. It has also improved the quality of life, reduced mortality, and decreased the incidence of AIDS and HIV-related conditions. Currently, however, affected individuals are typically on a lifetime course of several therapeutic drugs, all with the potential for associated toxicity and emergence of resistance. This calls for development of novel, potent, and broad anti-HIV agents able to stop the spread of HIV/AIDS. Significant progress has been made toward identification of anti-HIV-1 broadly neutralizing antibodies (bNAbs). However, antibody-based drugs are costly to produce and store. Administration (by injection only) and other obstacles limit clinical use. In recent years, several highly promising small-molecule HIV-1 entry inhibitors targeting the epitopes of bNAbs have been developed. These newly developed compounds are the focus of the present article.
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