自身免疫
表型
免疫学
自噬
细胞代谢
细胞生物学
生物
分泌物
自身抗体
细胞因子
B细胞
抗原呈递
免疫系统
细胞
T细胞
基因
内分泌学
抗体
遗传学
细胞凋亡
作者
Iwan G. A. Raza,Alexander J. Clarke
标识
DOI:10.3389/fimmu.2021.681105
摘要
B cells are central to the pathogenesis of multiple autoimmune diseases, through antigen presentation, cytokine secretion, and the production of autoantibodies. During development and differentiation, B cells undergo drastic changes in their physiology. It is emerging that these are accompanied by equally significant shifts in metabolic phenotype, which may themselves also drive and enforce the functional properties of the cell. The dysfunction of B cells during autoimmunity is characterised by the breaching of tolerogenic checkpoints, and there is developing evidence that the metabolic state of B cells may contribute to this. Determining the metabolic phenotype of B cells in autoimmunity is an area of active study, and is important because intervention by metabolism-altering therapeutic approaches may represent an attractive treatment target.
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