Department of Molecular Biology & Microbiology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Curr Opin HIV AIDS. 2024 May 1;19(3):102-109. doi: 10.1097/COH.0000000000000850. Epub 2024 Mar 12.
This review highlights advances in understanding the epigenetic control mechanisms that regulate HIV-1 latency mechanisms in T-cells and microglial cells and describes the potential of current therapeutic approaches targeting the epigenetic machinery to eliminate or block the HIV-1 latent reservoir.
Large-scale unbiased CRISPR-Cas9 library-based screenings, coupled with biochemical studies, have comprehensively identified the epigenetic factors pivotal in regulating HIV-1 latency, paving the way for potential novel targets in therapeutic development. These studies also highlight how the bivalency observed at the HIV-1 5'LTR primes latent proviruses for rapid reactivation.
The HIV-1 latent is established very early during infection, and its persistence is the major obstacle to achieving an HIV-1 cure. Here, we present a succinct summary of the latest research findings, shedding light on the pivotal roles played by host epigenetic machinery in the control of HIV-1 latency. Newly uncovered mechanisms permitting rapid reversal of epigenetic restrictions upon viral reactivation highlight the formidable challenges of achieving enduring and irreversible epigenetic silencing of HIV-1.
本文重点介绍了在理解调控 T 细胞和小神经胶质细胞中 HIV-1 潜伏机制的表观遗传控制机制方面的进展,并描述了当前靶向表观遗传机制的治疗方法消除或阻断 HIV-1 潜伏库的潜力。
基于大规模无偏 CRISPR-Cas9 文库的筛选,结合生化研究,全面鉴定了调控 HIV-1 潜伏的关键表观遗传因子,为治疗开发中的潜在新靶点铺平了道路。这些研究还强调了 HIV-1 5'LTR 观察到的二价性如何为潜伏前病毒的快速激活做好准备。
HIV-1 潜伏在感染早期就已建立,其持续存在是实现 HIV-1 治愈的主要障碍。在这里,我们简要总结了最新的研究发现,阐明了宿主表观遗传机制在控制 HIV-1 潜伏中的关键作用。新发现的机制允许在病毒重新激活时快速逆转表观遗传限制,突出了实现 HIV-1 持久和不可逆的表观遗传沉默所面临的巨大挑战。