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将人类免疫缺陷病毒/猴免疫缺陷病毒发病机制搞得一团糟:免疫细胞耗竭实验作为一种工具,用于理解 HIV 感染中的免疫保护相关性和致病性的免疫相关性。

Making a Monkey out of Human Immunodeficiency Virus/Simian Immunodeficiency Virus Pathogenesis: Immune Cell Depletion Experiments as a Tool to Understand the Immune Correlates of Protection and Pathogenicity in HIV Infection.

机构信息

Department of Pathology, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15261, USA.

Department of Infectious Diseases and Microbiology, School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261, USA.

出版信息

Viruses. 2024 Jun 17;16(6):972. doi: 10.3390/v16060972.

Abstract

Understanding the underlying mechanisms of HIV pathogenesis is critical for designing successful HIV vaccines and cure strategies. However, achieving this goal is complicated by the virus's direct interactions with immune cells, the induction of persistent reservoirs in the immune system cells, and multiple strategies developed by the virus for immune evasion. Meanwhile, HIV and SIV infections induce a pandysfunction of the immune cell populations, making it difficult to untangle the various concurrent mechanisms of HIV pathogenesis. Over the years, one of the most successful approaches for dissecting the immune correlates of protection in HIV/SIV infection has been the in vivo depletion of various immune cell populations and assessment of the impact of these depletions on the outcome of infection in non-human primate models. Here, we present a detailed analysis of the strategies and results of manipulating SIV pathogenesis through in vivo depletions of key immune cells populations. Although each of these methods has its limitations, they have all contributed to our understanding of key pathogenic pathways in HIV/SIV infection.

摘要

了解 HIV 发病机制的潜在机制对于设计成功的 HIV 疫苗和治疗策略至关重要。然而,由于病毒与免疫细胞的直接相互作用、免疫系统细胞中持续储库的诱导以及病毒为免疫逃避而开发的多种策略,实现这一目标变得复杂。同时,HIV 和 SIV 感染诱导免疫细胞群体的全面功能障碍,使得难以理清 HIV 发病机制的各种并发机制。多年来,剖析 HIV/SIV 感染中免疫保护相关因素的最成功方法之一是在体内耗尽各种免疫细胞群体,并评估这些耗竭对非人类灵长类动物模型中感染结局的影响。在这里,我们详细分析了通过体内耗尽关键免疫细胞群体来操纵 SIV 发病机制的策略和结果。尽管每种方法都有其局限性,但它们都有助于我们理解 HIV/SIV 感染中的关键致病途径。

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