Yang Wenjing, Yu Tianming, Cong Yingzi
Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Precis Clin Med. 2022 Jul 6;5(3):pbac018. doi: 10.1093/pcmedi/pbac018. eCollection 2022 Sep.
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.
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。