HIV感染者衰老及衰老相关共病的发病机制:HIV ACTION研讨会要点

Pathogenesis of Aging and Age-related Comorbidities in People with HIV: Highlights from the HIV ACTION Workshop.

作者信息

Gabuzda Dana, Jamieson Beth D, Collman Ronald G, Lederman Michael M, Burdo Tricia H, Deeks Steven G, Dittmer Dirk P, Fox Howard S, Funderburg Nicholas T, Pahwa Savita G, Pandrea Ivona, Wilson Cara C, Hunt Peter W

机构信息

Department of Cancer Immunology and Virology; Dana-Farber Cancer Institute; Boston, Massachusetts; Department of Neurology; Harvard Medical School; Boston, Massachusetts.

Department of Medicine; David Geffen School of Medicine; University of California; Los Angeles, California.

出版信息

Pathog Immun. 2020 Jun 17;5(1):143-174. doi: 10.20411/pai.v5i1.365. eCollection 2020.

Abstract

People with HIV (PWH) experience accentuated biological aging, as defined by markers of inflammation, immune dysfunction, and the epigenetic clock. They also have an elevated risk of multiple age-associated comorbidities. To discuss current knowledge, research gaps, and priorities in aging and age-related comorbidities in treated HIV infection, the NIH program staff organized a workshop held in Bethesda, Maryland in September 2019. This review article describes highlights of discussions led by the Pathogenesis/Basic Science Research working group that focused on three high priority topics: immunopathogenesis; the microbiome/virome; and aging and senescence. We summarize knowledge in these fields and describe key questions for research on the pathogenesis of aging and age-related comorbidities in PWH. Understanding the drivers and mechanisms underlying accentuated biological aging is a high priority that will help identify potential therapeutic targets to improve healthspan in older PWH.

摘要

人类免疫缺陷病毒感染者(PWH)会经历加速的生物衰老,这是由炎症、免疫功能障碍和表观遗传时钟等标志物所定义的。他们还面临多种与年龄相关的合并症风险升高的问题。为了探讨接受治疗的HIV感染中衰老及与年龄相关合并症的现有知识、研究差距和优先事项,美国国立卫生研究院(NIH)项目工作人员于2019年9月在马里兰州贝塞斯达组织了一次研讨会。这篇综述文章描述了发病机制/基础科学研究工作组主导的讨论要点,该工作组聚焦于三个高度优先的主题:免疫发病机制;微生物组/病毒组;以及衰老和细胞衰老。我们总结了这些领域的知识,并描述了关于PWH衰老和与年龄相关合并症发病机制研究的关键问题。了解加速生物衰老的驱动因素和机制是一个高度优先事项,这将有助于确定潜在的治疗靶点,以改善老年PWH的健康寿命。

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