Centre for Inflammation Research, University of Edinburgh, Edinburgh, UK.
Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, Canada.
Cell Mol Life Sci. 2022 Jul 7;79(8):402. doi: 10.1007/s00018-022-04433-9.
Age-associated B cells (ABCs) are a transcriptionally and functionally unique B cell population. In addition to arising with age and following infection, ABCs are expanded during autoimmune disease, including those with systemic lupus erythematosus, multiple sclerosis, and rheumatoid arthritis. The exact nature of how ABCs impact disease remains unclear. Here, we review what is known regarding ABC development and distribution during diseases including systemic lupus erythematosus, multiple sclerosis, and rheumatoid arthritis. We discuss possible mechanisms by which ABCs could contribute to disease, including the production of cytokines and autoantibodies or stimulation of T cells. Finally, we speculate on how ABCs might act as mediators between sex, infection, and autoimmune disease, and discuss avenues for further research.
与年龄相关的 B 细胞(ABCs)是一种转录和功能上独特的 B 细胞群体。除了随年龄增长和感染而出现外,ABCs 在自身免疫性疾病中也会扩增,包括系统性红斑狼疮、多发性硬化症和类风湿关节炎。ABCs 如何影响疾病的确切性质尚不清楚。在这里,我们回顾了在包括系统性红斑狼疮、多发性硬化症和类风湿关节炎在内的疾病中 ABC 发育和分布的已知情况。我们讨论了 ABCs 可能导致疾病的几种机制,包括细胞因子和自身抗体的产生或 T 细胞的刺激。最后,我们推测 ABCs 如何在性别、感染和自身免疫性疾病之间充当介质,并讨论进一步研究的途径。