蛋白酶
炎症体
上睑下垂
逆转录酶
病毒学
生物
程序性细胞死亡
蛋白质水解
半胱氨酸蛋白酶
细胞内
NLRP1
细胞生物学
人类免疫缺陷病毒(HIV)
先天免疫系统
细胞凋亡
免疫系统
核糖核酸
酶
生物化学
免疫学
受体
基因
作者
Qiankun Wang,Hongbo Gao,Kolin M. Clark,Christian Shema Mugisha,Keanu Davis,Jack Pengfei Tang,Gray H. Harlan,Carl J. DeSelm,Rachel M. Presti,Sebla B. Kutluay,Liang Shan
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2021-02-04
卷期号:371 (6535)
被引量:105
标识
DOI:10.1126/science.abe1707
摘要
HIV-1 has high mutation rates and exists as mutant swarms within the host. Rapid evolution of HIV-1 allows the virus to outpace the host immune system, leading to viral persistence. Approaches to targeting immutable components are needed to clear HIV-1 infection. Here, we report that the caspase recruitment domain-containing protein 8 (CARD8) inflammasome senses HIV-1 protease activity. HIV-1 can evade CARD8 sensing because its protease remains inactive in infected cells before viral budding. Premature intracellular activation of the viral protease triggered CARD8 inflammasome-mediated pyroptosis of HIV-1-infected cells. This strategy led to the clearance of latent HIV-1 in patient CD4+ T cells after viral reactivation. Thus, our study identifies CARD8 as an inflammasome sensor of HIV-1, which holds promise as a strategy for the clearance of persistent HIV-1 infection.
科研通智能强力驱动
Strongly Powered by AbleSci AI