HIV-1 亚型和潜伏库。

Current opinion in HIV and AIDS Pub Date : 2024-03-01 Epub Date: 2023-12-11 DOI:10.1097/COH.0000000000000835
Udaykumar Ranga, Arun Panchapakesan, Chhavi Saini
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引用次数: 0

摘要

综述的目的:我们探讨了 HIV-1 亚型特异性变异及其对 HIV-1 潜伏期影响的研究现状。我们还简要讨论了围绕管理 HIV-1 转录的开/关状态的决策过程的争议,特别侧重于调控元件、长末端重复(LTR)和 Tat。了解决策过程对于制定有效的干预策略(如 "冲击-杀死 "方法)以重新激活潜伏的 HIV-1 病毒至关重要:亚型特异性转录因子结合位点(TFBS)变异以及这些变异对病毒潜伏期可能产生的影响已引起人们的关注。此外,还开发了多种亚型特异性检测方法来量化潜伏病毒库。一个有趣的观察结果是,与其他病毒亚型相比,HIV-1B 感染的潜伏病毒库相对较大,这需要严格的验证。据报道,HIV-1C 中出现了 LTR 变异病毒株,其潜伏逆转的程度明显更高。总结:尽管做出了不懈的大量努力,但潜伏的 HIV-1 仍是功能性治愈的一个巨大挑战。我们需要坚定不移地继续努力,以了解 HIV-1 潜伏期的开/关决策过程,开发严格的检测方法以准确量化潜伏库,并确定有效的潜伏期逆转剂和针对多个潜伏期阶段的鸡尾酒疗法。综述强调了将不同病毒亚型纳入未来潜伏期研究的重要性。
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HIV-1 subtypes and latent reservoirs.

Purpose of review: We explore the current status of research on HIV-1 subtype-specific variations and their impact on HIV-1 latency. We also briefly address the controversy surrounding the decision-making process governing the ON/OFF states of HIV-1 transcription, specifically focusing on the regulatory elements, the long terminal repeat (LTR), and Tat. Understanding the decision-making process is crucial for developing effective intervention strategies, such as the 'shock-and-kill' approach, to reactivate latent HIV-1.

Recent findings: Attention has been drawn to subtype-specific transcription factor binding site (TFBS) variations and the possible impact of these variations on viral latency. Further, diverse subtype-specific assays have been developed to quantify the latent viral reservoirs. One interesting observation is the relatively larger latent reservoirs in HIV-1B infection than those of other viral subtypes, which needs rigorous validation. The emergence of LTR-variant viral strains in HIV-1C demonstrating significantly higher levels of latency reversal has been reported.

Summary: Despite persistent and substantial efforts, latent HIV-1 remains a formidable challenge to a functional cure. Determined and continued commitment is needed to understand the ON/OFF decision-making process of HIV-1 latency, develop rigorous assays for accurately quantifying the latent reservoirs, and identify potent latency-reversing agents and cocktails targeting multiple latency stages. The review emphasizes the importance of including diverse viral subtypes in future latency research.

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