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线粒体调控的调节性 T 细胞:中枢神经系统自身免疫性疾病的潜在治疗靶点。

Mitochondrial-regulated Tregs: potential therapeutic targets for autoimmune diseases of the central nervous system.

机构信息

Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Department of Clinical Laboratory, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Front Immunol. 2023 Dec 12;14:1301074. doi: 10.3389/fimmu.2023.1301074. eCollection 2023.

DOI:10.3389/fimmu.2023.1301074
PMID:38149252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10749924/
Abstract

Regulatory T cells (Tregs) can eliminate autoreactive lymphocytes, induce self-tolerance, and suppress the inflammatory response. Mitochondria, as the energy factories of cells, are essential for regulating the survival, differentiation, and function of Tregs. Studies have shown that patients with autoimmune diseases of the central nervous system, such as multiple sclerosis, neuromyelitis optica spectrum disorder, and autoimmune encephalitis, have aberrant Tregs and mitochondrial damage. However, the role of mitochondrial-regulated Tregs in autoimmune diseases of the central nervous system remains inconclusive. Therefore, this study reviews the mitochondrial regulation of Tregs in autoimmune diseases of the central nervous system and investigates the possible mitochondrial therapeutic targets.

摘要

调节性 T 细胞(Tregs)可以消除自身反应性淋巴细胞,诱导自身耐受,并抑制炎症反应。线粒体作为细胞的能量工厂,对于调节 Tregs 的存活、分化和功能至关重要。研究表明,多发性硬化症、视神经脊髓炎谱系疾病和自身免疫性脑炎等中枢神经系统自身免疫性疾病患者存在异常的 Tregs 和线粒体损伤。然而,线粒体调节的 Tregs 在中枢神经系统自身免疫性疾病中的作用尚不清楚。因此,本研究综述了 Tregs 在线粒体调节中枢神经系统自身免疫性疾病中的作用,并探讨了可能的线粒体治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef35/10749924/d034e7c03111/fimmu-14-1301074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef35/10749924/1b767e004058/fimmu-14-1301074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef35/10749924/d034e7c03111/fimmu-14-1301074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef35/10749924/1b767e004058/fimmu-14-1301074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef35/10749924/d034e7c03111/fimmu-14-1301074-g002.jpg

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本文引用的文献

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Nat Rev Immunol. 2023 Mar;23(3):159-173. doi: 10.1038/s41577-022-00760-x. Epub 2022 Jul 25.
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Oxidized DNA fragments exit mitochondria via mPTP- and VDAC-dependent channels to activate NLRP3 inflammasome and interferon signaling.氧化的 DNA 片段通过 mPTP 和 VDAC 依赖性通道从线粒体中逸出,以激活 NLRP3 炎性体和干扰素信号。
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Front Immunol. 2021 Oct 5;12:750542. doi: 10.3389/fimmu.2021.750542. eCollection 2021.
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Regulatory T cells protect against brain damage by alleviating inflammatory response in neuromyelitis optica spectrum disorder.调节性 T 细胞通过减轻视神经脊髓炎谱系疾病中的炎症反应来保护大脑免受损伤。
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