Department of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, United Kingdom.
Immune and Infectious Disease Division, Academic Department of Pediatrics (DPUO), Bambino Gesù Children's Hospital, Rome, Italy.
Front Cell Infect Microbiol. 2020 Apr 7;10:134. doi: 10.3389/fcimb.2020.00134. eCollection 2020.
HIV-1 eradication strategies aim to achieve viral remission in the absence of antiretroviral therapy (ART). The development of an HIV-1 cure remains challenging due to the latent reservoir (LR): long-lived CD4 T cells that harbor transcriptionally silent HIV-1 provirus. The LR is stable despite years of suppressive ART and is the source of rebound viremia following therapy interruption. Cure strategies such as "shock and kill" aim to eliminate or reduce the LR by reversing latency, exposing the infected cells to clearance via the immune response or the viral cytopathic effect. Alternative strategies include therapeutic vaccination, which aims to prime the immune response to facilitate control of the virus in the absence of ART. Despite promising advances, these strategies have been unable to significantly reduce the LR or increase the time to viral rebound but have provided invaluable insight in the field of HIV-1 eradication. The development and assessment of an HIV-1 cure requires robust assays that can measure the LR with sufficient sensitivity to detect changes that may occur following treatment. The viral outgrowth assay (VOA) is considered the gold standard method for LR quantification due to its ability to distinguish intact and defective provirus. However, the VOA is time consuming and resource intensive, therefore several alternative assays have been developed to bridge the gap between practicality and accuracy. Whilst a cure for HIV-1 infection remains elusive, recent advances in our understanding of the LR and methods for its eradication have offered renewed hope regarding achieving ART free viral remission.
HIV-1 清除策略旨在在没有抗逆转录病毒疗法 (ART) 的情况下实现病毒缓解。由于潜伏库 (LR) 的存在,HIV-1 治愈的发展仍然具有挑战性:长期存活的 CD4 T 细胞中含有转录沉默的 HIV-1 前病毒。尽管经过多年的抑制性 ART,LR 仍然稳定,并且是治疗中断后病毒血症反弹的来源。“冲击和杀伤”等清除策略旨在通过逆转潜伏来消除或减少 LR,通过免疫反应或病毒细胞病变效应使受感染的细胞暴露于清除之下。替代策略包括治疗性疫苗接种,旨在启动免疫反应,以促进在没有 ART 的情况下控制病毒。尽管取得了有希望的进展,但这些策略未能显著减少 LR 或增加病毒反弹的时间,但为 HIV-1 清除领域提供了宝贵的见解。HIV-1 治愈的开发和评估需要灵敏的检测方法,这些方法可以足够灵敏地测量 LR,以检测治疗后可能发生的变化。病毒扩增测定 (VOA) 被认为是 LR 定量的金标准方法,因为它能够区分完整和缺陷的前病毒。然而,VOA 既耗时又耗费资源,因此已经开发了几种替代检测方法来弥合实用性和准确性之间的差距。虽然 HIV-1 感染的治愈仍然难以捉摸,但我们对 LR 的理解以及清除 LR 的方法的最新进展为实现无 ART 的病毒缓解带来了新的希望。