MAIT细胞在抗结核分枝杆菌免疫中的作用

Z H Cao, X X Cheng
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引用次数: 0

摘要

mucal -associated invariant T cells (MAIT cells)是一类广泛分布于人体内的先天性免疫样T细胞。在感染过程中,微生物合成的维生素B代谢物等抗原通过MR1(主要组织相容性复合体类Ⅰ样分子)呈递给MAIT细胞,MAIT细胞被激活,通过释放细胞因子和细胞毒分子发挥抗菌、抗病毒、抗癌和组织修复作用。动物和体外研究表明,活动性肺结核患者外周血中的MAIT细胞数量减少,细胞表现出功能衰竭表型。MAIT细胞被结核分枝杆菌抗原激活,产生炎性细胞因子如TNF-α、IFN-γ和细胞毒性分子如颗粒酶B,发挥mr1依赖性和细胞因子依赖性的抗结核作用。此外,MAIT细胞也可以作为先天免疫和获得性免疫之间的桥梁,通过启动传统的t细胞反应。目前,针对MAIT细胞的疫苗和药物也有相关的实验研究,在结核病的预防和控制中显示出巨大的潜力。本文将对MAIT细胞的发现、分类、发育和活化、在结核分枝杆菌感染中的作用及其在结核病防治中的应用进行综述,以期为结核病防治提供新的免疫靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Role of MAIT cells in immunity against Mycobacterium tuberculosis].

Mucosal-associated invariant T cells (MAIT cells) are a class of innate immune-like T cells that are widely distributed in the human body. During infection, antigens such as vitamin B metabolites synthesized by microorganisms are presented to MAIT cells by MR1 (major histocompatibility complex class Ⅰ-like molecule), and MAIT cells are activated and exert antibacterial, antiviral, anticancer and tissue repair effects by releasing cytokines and cytotoxic molecules. Animal and in vitro studies have shown that the number of MAIT cells in the peripheral blood of patients with active tuberculosis is reduced and the cells exhibit a functional exhaustion phenotype. MAIT cells are activated by Mycobacterium tuberculosis antigens and produce inflammatory cytokines such as TNF-α, IFN-γ and cytotoxic molecules such as granzyme B to exert anti-tuberculosis effects that are MR1-dependent and cytokine-dependent. In addition, MAIT cells can also act as a bridge between innate and acquired immunity by initiating a conventional T-cell response. Currently, there are also relevant experimental studies on vaccines and drugs targeting MAIT cells, which show great potential in the prevention and control of tuberculosis. In this article, we will review the discovery and grouping, development and activation of MAIT cells, their role in Mycobacterium tuberculosis infection, and their application in tuberculosis prevention and treatment, in order to provide new immunological targets for tuberculosis prevention and treatment.

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