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HIV-1疾病中黏膜相关恒定T细胞的损耗与重建

MAIT Cell Loss and Reconstitution in HIV-1 Disease.

作者信息

Han Fei, Zheng Yichao, Ho Amanda, Ma Shaohua, Sandberg Johan K, Leeansyah Edwin

机构信息

Institute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.

Institute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China; Precision Medicine and Healthcare Research Centre, Tsinghua-Berkeley Shenzhen Institute, Tsinghua University, Shenzhen 518055, China.

出版信息

Crit Rev Immunol. 2021;41(5):69-82. doi: 10.1615/CritRevImmunol.2022042906.

Abstract

Mucosa-associated invariant T (MAIT) cells are unconventional innate-like T cells that recognize microbial riboflavin-related metabolites presented by the evolutionarily conserved MHC class I-related (MR1) molecule. MAIT cells are abundant in circulation and mucosal tissues and are poised to mount rapid effector responses against diverse microbial organisms. Despite the absence of virally encoded riboflavin-related metabolite antigens, MAIT cells can respond to viral infections in an MR1-independent and cytokine-dependent manner. In chronic HIV-1 infection, MAIT cells are persistently depleted and functionally exhausted. Long-term effective combination antiretroviral therapy can only partially rescue MAIT cell numbers and dysfunction. Our understanding of the mechanisms underlying MAIT cell loss in HIV-1 infection is still incomplete, and to date, few effective strategies to recover their loss in humans are available. Here, we review current knowledge concerning the mechanisms of MAIT cell responses and loss in different stages of HIV-1 infection and how we may potentially develop strategies to restore these cells in the clinical setting. We further discuss novel strategies that may aid future investigations into MAIT cell immunobiology in HIV-1 infection, including the potential use of three-dimensional organoid models to dissect the mechanisms of MAIT cell depletion and to explore interventions that may restore their numbers and functionality.

摘要

黏膜相关恒定T(MAIT)细胞是一类非常规的固有样T细胞,可识别由进化上保守的MHC I类相关(MR1)分子呈递的微生物核黄素相关代谢产物。MAIT细胞在循环系统和黏膜组织中含量丰富,随时准备对多种微生物病原体发起快速的效应反应。尽管缺乏病毒编码的核黄素相关代谢产物抗原,但MAIT细胞可通过不依赖MR1且依赖细胞因子的方式对病毒感染作出反应。在慢性HIV-1感染中,MAIT细胞持续耗竭且功能衰竭。长期有效的联合抗逆转录病毒疗法只能部分挽救MAIT细胞数量及功能障碍。我们对HIV-1感染中MAIT细胞丢失机制的理解仍不完整,迄今为止,几乎没有有效的策略可恢复人类体内MAIT细胞的丢失。在此,我们综述了关于HIV-1感染不同阶段MAIT细胞反应及丢失机制的现有知识,以及在临床环境中恢复这些细胞的潜在策略。我们还进一步讨论了可能有助于未来对HIV-1感染中MAIT细胞免疫生物学进行研究的新策略,包括潜在使用三维类器官模型来剖析MAIT细胞耗竭机制,并探索可能恢复其数量和功能的干预措施。

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