Leong Yew Ann, Atnerkar Anurag, Yu Di
Infection and Immunity Program, Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia.
Department of Immunology and Infectious Disease, John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.
Front Immunol. 2017 May 31;8:622. doi: 10.3389/fimmu.2017.00622. eCollection 2017.
Human immunodeficiency virus (HIV) infects millions of people worldwide, and new cases continue to emerge. Once infected, the virus cannot be cleared by the immune system and causes acquired immunodeficiency syndrome. Combination antiretroviral therapeutic regimen effectively suppresses viral replication and halts disease progression. The treatment, however, does not eliminate the virus-infected cells, and interruption of treatment inevitably leads to viral rebound. The rebound virus originates from a group of virus-infected cells referred to as the cellular reservoir of HIV. Identifying and eliminating the HIV reservoir will prevent viral rebound and cure HIV infection. In this review, we focus on a recently discovered HIV reservoir in a subset of CD4 T cells called the follicular helper T (T) cells. We describe the potential mechanisms for the emergence of reservoir in T cells, and the strategies to target and eliminate this viral reservoir.
人类免疫缺陷病毒(HIV)感染了全球数百万人,新病例仍在不断出现。一旦感染,该病毒无法被免疫系统清除,并会导致获得性免疫缺陷综合征。联合抗逆转录病毒治疗方案可有效抑制病毒复制并阻止疾病进展。然而,这种治疗并不能消除被病毒感染的细胞,治疗中断不可避免地会导致病毒反弹。反弹的病毒源自一组被称为HIV细胞储存库的病毒感染细胞。识别并消除HIV储存库将预防病毒反弹并治愈HIV感染。在本综述中,我们重点关注最近在一类称为滤泡辅助性T(Th)细胞的CD4 T细胞亚群中发现的HIV储存库。我们描述了T细胞中储存库出现的潜在机制,以及靶向和消除这种病毒储存库的策略。