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1
CD8 T cells control SIV infection using both cytolytic effects and non-cytolytic suppression of virus production.CD8 T 细胞通过细胞溶解作用和非细胞溶解抑制病毒产生来控制 SIV 感染。
Nat Commun. 2023 Oct 20;14(1):6657. doi: 10.1038/s41467-023-42435-8.
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T cell activation is insufficient to drive SIV disease progression.T 细胞激活不足以驱动 SIV 疾病进展。
JCI Insight. 2023 Jul 24;8(14):e161111. doi: 10.1172/jci.insight.161111.
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Prolonged experimental CD4 T-cell depletion does not cause disease progression in SIV-infected African green monkeys.长期的实验性 CD4 T 细胞耗竭不会导致 SIV 感染的非洲绿猴疾病进展。
Nat Commun. 2023 Feb 22;14(1):979. doi: 10.1038/s41467-023-36379-2.
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CD8 lymphocytes do not impact SIV reservoir establishment under ART.在 ART 治疗下,CD8 淋巴细胞不会影响 SIV 储存库的建立。
Nat Microbiol. 2023 Feb;8(2):299-308. doi: 10.1038/s41564-022-01311-9. Epub 2023 Jan 23.
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Natural Killer Cells Regulate Acute SIV Replication, Dissemination, and Inflammation, but Do Not Impact Independent Transmission Events.自然杀伤细胞调节急性 SIV 复制、传播和炎症,但不影响独立的传播事件。
J Virol. 2023 Jan 31;97(1):e0151922. doi: 10.1128/jvi.01519-22. Epub 2022 Dec 13.
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I've looked at gut from both sides now: Gastrointestinal tract involvement in the pathogenesis of SARS-CoV-2 and HIV/SIV infections.我现在从正反两方面看待肠道:胃肠道在 SARS-CoV-2 和 HIV/SIV 感染发病机制中的作用。
Front Immunol. 2022 Aug 12;13:899559. doi: 10.3389/fimmu.2022.899559. eCollection 2022.
7
Strategies for HIV-1 vaccines that induce broadly neutralizing antibodies.诱导广泛中和抗体的 HIV-1 疫苗策略。
Nat Rev Immunol. 2023 Mar;23(3):142-158. doi: 10.1038/s41577-022-00753-w. Epub 2022 Aug 12.
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NK cell spatial dynamics and IgA responses in gut-associated lymphoid tissues during SIV infections.SIV 感染期间肠道相关淋巴组织中 NK 细胞的空间动态和 IgA 反应。
Commun Biol. 2022 Jul 7;5(1):674. doi: 10.1038/s42003-022-03619-y.
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Therapeutic efficacy of combined active and passive immunization in ART-suppressed, SHIV-infected rhesus macaques.联合主动和被动免疫在抗逆转录病毒治疗抑制、SHIV 感染恒河猴中的治疗效果。
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Learning to Be Elite: Lessons From HIV-1 Controllers and Animal Models on Trained Innate Immunity and Virus Suppression.学习成为精英:从 HIV-1 控制器和动物模型中获得的关于训练有素的先天免疫和病毒抑制的经验教训。
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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.

DOI:10.3390/v16060972
PMID:38932264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11209256/
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。