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Characterizing the Latent HIV-1 Reservoir in Patients with Viremia Suppressed on cART: Progress, Challenges, and Opportunities

机译:表征患者患者患者的潜伏HIV-1储层压制推车:进步,挑战和机遇

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摘要

Modem combination antiretroviral therapy (cART) can bring HIV-1 in blood plasma to level undetectable by standard tests, prevent the onset of acquired immune deficiency syndrome (AIDS), and allow a near-normal life expectancy for HIV-infected individuals. Unfortunately, cART is not curative, as within a few weeks of treatment cessation, HIV viremia in most patients rebounds to pre-cART levels. The primary source of this rebound, and the principal barrier to a cure, is the highly stable reservoir of latent yet replication-competent HIV-1 proviruses integrated into the genomic DNA of resting memory CD4+ T cells. In this review, prevailing models for how the latent reservoir is established and maintained, residual viremia and viremic rebound upon withdrawal of cART, and the types and characteristics of cells harboring latent HIV-1 will be discussed. Selected technologies currently being used to advance our understanding of HIV latency will also be presented, as will a perspective on which areas of advancement are most essential for producing the next generation of HIV-1 therapeutics.
机译:调制解调器组合抗逆转录病毒治疗(推车)可以通过标准试验抑制血浆中的HIV-1,防止获得的免疫缺陷综合征(艾滋病)的发作,并允许艾滋病毒感染的个体的近似预期寿命。不幸的是,推车不是治愈性的,如在治疗停止的几周内,大多数患者的艾滋病病毒血症率篮板前率呈现给购物车前水平。这种反弹的主要来源和治愈的主要障碍是潜在的尚未复制竞争力的HIV-1潜水液的高度稳定储层集成到静置记忆CD4 + T细胞的基因组DNA中。在本综述中,如何在撤回购物车时确定和维持潜伏储存器和维持,残留的病毒血症和病毒新反弹的普遍模型,以及潜在HIV-1的细胞的类型和特征将进行讨论。目前正在习惯推进我们对HIV延迟理解的所选技术,也将是哪些进步领域对生产下一代HIV-1治疗方法至关重要的观点。

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