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CD4 T细胞代谢、肠道微生物群与自身免疫性疾病:对自身免疫性疾病精准医学的启示

CD4 T cell metabolism, gut microbiota, and autoimmune diseases: implication in precision medicine of autoimmune diseases.

作者信息

Yang Wenjing, Yu Tianming, Cong Yingzi

机构信息

Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.

出版信息

Precis Clin Med. 2022 Jul 6;5(3):pbac018. doi: 10.1093/pcmedi/pbac018. eCollection 2022 Sep.

Abstract

CD4 T cells are critical to the development of autoimmune disorders. Glucose, fatty acids, and glutamine metabolisms are the primary metabolic pathways in immune cells, including CD4 T cells. The distinct metabolic programs in CD4 T cell subsets are recognized to reflect the bioenergetic requirements, which are compatible with their functional demands. Gut microbiota affects T cell responses by providing a series of antigens and metabolites. Accumulating data indicate that CD4 T cell metabolic pathways underlie aberrant T cell functions, thereby regulating the pathogenesis of autoimmune disorders, including inflammatory bowel diseases, systemic lupus erythematosus, and rheumatoid arthritis. Here, we summarize the current progress of CD4 T cell metabolic programs, gut microbiota regulation of T cell metabolism, and T cell metabolic adaptions to autoimmune disorders to shed light on potential metabolic therapeutics for autoimmune diseases.

摘要

CD4 T细胞对自身免疫性疾病的发展至关重要。葡萄糖、脂肪酸和谷氨酰胺代谢是免疫细胞(包括CD4 T细胞)中的主要代谢途径。CD4 T细胞亚群中不同的代谢程序被认为反映了生物能量需求,这与其功能需求相匹配。肠道微生物群通过提供一系列抗原和代谢产物来影响T细胞反应。越来越多的数据表明,CD4 T细胞代谢途径是异常T细胞功能的基础,从而调节自身免疫性疾病(包括炎症性肠病、系统性红斑狼疮和类风湿性关节炎)的发病机制。在此,我们总结了CD4 T细胞代谢程序、肠道微生物群对T细胞代谢的调节以及T细胞对自身免疫性疾病的代谢适应方面的当前进展,以阐明自身免疫性疾病潜在的代谢疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff19/9384833/1550af72b96b/pbac018fig1.jpg

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