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T 细胞耗竭的代谢可塑性和调控。

Metabolic plasticity and regulation of T cell exhaustion.

机构信息

Gansu Provincial Key Laboratory of Evidence-Based Medicine and Clinical Translation & Lanzhou Center for Tuberculosis Research, Institute of Pathogen Biology, School of Basic Medical Sciences, Lanzhou University, Lanzhou, China.

Department of gynecology and obstetrics, Gansu Provincial Hospital, Lanzhou, China.

出版信息

Immunology. 2022 Dec;167(4):482-494. doi: 10.1111/imm.13575. Epub 2022 Sep 30.

Abstract

The metabolic reprogramming during T cell activation and differentiation affects T cell fate and immune responses. Cell metabolism may serve as the driving force that induces epigenetic modifications, contributing to regulating T cell differentiation. Persistent pathogen infection leads to T cell exhaustion, which is composed of two main subsets and with distinct metabolic characteristics. The progenitor exhausted T cells utilize mitochondrial fatty acid oxidation (FAO) and oxidative phosphorylation (OXPHOS) for energy, while terminally exhausted T cells mainly rely on glycolytic metabolism with impaired glycolysis and OXPHOS. Here, we compiled the latest research on how T cell metabolism defines differentiation, focusing on T cell exhaustion during chronic infections. In addition, metabolic-related factors including antigen stimulation signals strength, cytokines and epigenetics affecting T cell exhaustion were also reviewed. Furthermore, the intervention strategies on metabolism and epigenetics to reverse T cell exhaustion were discussed in detail, which may contribute to achieving the goal of prevention and treatment of T cell exhaustion.

摘要

T 细胞激活和分化过程中的代谢重编程影响 T 细胞命运和免疫反应。细胞代谢可以作为诱导表观遗传修饰的驱动力,有助于调节 T 细胞分化。持续性病原体感染导致 T 细胞耗竭,其由两个主要亚群组成,具有不同的代谢特征。祖细胞耗竭 T 细胞利用线粒体脂肪酸氧化(FAO)和氧化磷酸化(OXPHOS)产生能量,而终末耗竭 T 细胞主要依赖糖酵解代谢,糖酵解和 OXPHOS 受损。在这里,我们整理了关于 T 细胞代谢如何定义分化的最新研究,重点关注慢性感染期间的 T 细胞耗竭。此外,还综述了包括抗原刺激信号强度、细胞因子和表观遗传学在内的代谢相关因素对 T 细胞耗竭的影响。此外,还详细讨论了代谢和表观遗传干预策略以逆转 T 细胞耗竭,这可能有助于实现预防和治疗 T 细胞耗竭的目标。

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