Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, Saint Louis, MO, USA.
Department of Molecular Microbiology, Washington University School of Medicine, Saint Louis, MO, USA.
Science. 2021 Mar 19;371(6535). doi: 10.1126/science.abe1707. Epub 2021 Feb 4.
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.
HIV-1 具有很高的突变率,在宿主中存在着突变群体。HIV-1 的快速进化使病毒能够超越宿主免疫系统,导致病毒持续存在。需要针对不可变成分的方法来清除 HIV-1 感染。在这里,我们报告了包含半胱氨酸天冬氨酸蛋白酶募集域的蛋白 8(CARD8)炎症小体感知 HIV-1 蛋白酶活性。HIV-1 可以逃避 CARD8 的感应,因为其蛋白酶在感染细胞中的病毒出芽之前保持非活性。病毒蛋白酶的过早细胞内激活触发了 CARD8 炎症小体介导的 HIV-1 感染细胞的细胞焦亡。这一策略导致潜伏 HIV-1 在病毒重新激活后从患者的 CD4 T 细胞中清除。因此,我们的研究确定 CARD8 是 HIV-1 的炎症小体传感器,作为清除持续性 HIV-1 感染的策略具有很大的潜力。