Martin Flavius, Chan Andrew C
Department of Immunology, Genentech, Inc., South San Francisco, California 94080, USA.
Annu Rev Immunol. 2006;24:467-96. doi: 10.1146/annurev.immunol.24.021605.090517.
The pathogenic roles of B cells in autoimmune diseases occur through several mechanistic pathways that include autoantibodies, immune complexes, dendritic and T cell activation, cytokine synthesis, chemokine-mediated functions, and ectopic neolymphogenesis. Each of these pathways participate to different degrees in autoimmune diseases. The use of B cell-targeted and B cell subset-targeted therapies in humans is illuminating the mechanisms at work in a variety of human autoimmune diseases. In this review, we highlight some of these recent findings that provide insights into both murine models of autoimmunity and human autoimmune diseases.
B细胞在自身免疫性疾病中的致病作用通过多种机制途径发生,包括自身抗体、免疫复合物、树突状细胞和T细胞活化、细胞因子合成、趋化因子介导的功能以及异位新淋巴生成。这些途径中的每一种在自身免疫性疾病中都有不同程度的参与。在人类中使用B细胞靶向和B细胞亚群靶向疗法正在阐明各种人类自身免疫性疾病中起作用的机制。在本综述中,我们重点介绍了一些最新发现,这些发现为自身免疫的小鼠模型和人类自身免疫性疾病提供了见解。