非人类灵长类动物模型对理解急性HIV-1感染的效用。

Current opinion in HIV and AIDS Pub Date : 2025-05-01 Epub Date: 2025-03-27 DOI:10.1097/COH.0000000000000920
Matthew S Parsons, Diane L Bolton
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引用次数: 0

摘要

综述目的:非人类灵长类动物(NHP) HIV-1感染模型为评估人类无法解决的急性HIV-1感染(AHI)方面提供了补充的实验途径。本文综述了过去18个月在siv感染或shiv感染猕猴物种中的急性感染研究。最近的研究发现:回顾了早期感染期间复制能力病毒库建立的动态,整个治疗过程中的库维持,以及停止治疗后影响病毒反弹的因素。还讨论了中枢神经系统和肝脏的急性感染事件以及这些事件与慢性感染期间合并症表现之间的潜在联系。其他研究探讨了急性感染期间发生的事件如何影响自然病毒控制或治疗后控制的发展。另一份报告评估了在急性感染期间使用具有增强能力的广泛中和抗体与先天免疫细胞结合的治疗,强调了这种早期干预形成先天和适应性抗病毒反应的能力。摘要:HIV-1感染的NHP模型是研究AHI事件的基础研究工具。这些模型能够详细描述发病机制,并测试假设驱动的策略,通过干预AHI期间改变病程,包括靶向病毒持久性和慢性感染期间持续存在的合并症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The utility of nonhuman primate models for understanding acute HIV-1 infection.

Purpose of review: Nonhuman primate (NHP) models of HIV-1 infection provide complementary experimental pathways for assessing aspects of acute HIV-1 infection (AHI) that cannot be addressed in humans. This article reviews acute infection studies in SIV-infected or SHIV-infected macaque species over the previous 18 months.

Recent findings: Reviewed studies examined the dynamics of replication-competent viral reservoir establishment during early infection, reservoir maintenance throughout therapy, and factors influencing viral rebound after treatment cessation. Also discussed are acute infection events in the central nervous system and liver and potential links between these events and manifestations of comorbidities during chronic infection. Additional studies addressed how occurrences during acute infection impact the development of natural viral control or posttreatment control. Another report evaluated treatment during acute infection with broadly neutralizing antibodies with enhanced ability to engage innate immune cells, highlighting the ability of this early intervention to shape innate and adaptive antiviral responses.

Summary: NHP models of HIV-1 infection are a fundamental research tool for investigating AHI events. These models enable detailed pathogenesis characterization and the testing of hypothesis-driven strategies for altering disease courses through interventions during AHI, including targeting viral persistence and comorbidities that persist throughout chronic infection.

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