Regulatory B cells in autoimmune diseases and mucosal immune homeostasis.

Regulatory B cells in autoimmune diseases and mucosal immune homeostasis.
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DOI:
10.3109/08916931003782189
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发表时间:
2011-02
期刊:
影响因子:
3.5
通讯作者:
Wei B
Wei B
中科院分区:
医学4区
文献类型:
--
作者:
Li X;Braun J;Wei B

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B淋巴细胞通过次级淋巴器官的器官发生、向T细胞呈递抗原、产生抗体和分泌细胞因子来促进生理免疫。它们在几种自身免疫性疾病中的作用也是众所周知的,主要是作为致病性抗体的产生者。然而,B细胞的某些亚群正在成为小鼠和人类中重要的调节细胞群。B细胞的调节功能已在多种自身免疫性疾病的小鼠模型中得到证实,所述自身免疫性疾病包括胶原诱导的关节炎(CIA)、实验性自身免疫性脑脊髓炎(EAE)、前房相关免疫偏离(ACAID)、糖尿病、接触性超敏反应(CHS)和肠粘膜炎症。从小鼠和人类研究中积累的证据证实了调节性B细胞的存在,并开始确定其作用机制。本文首先回顾了自身免疫性疾病中具有调节功能的B细胞的历史,并总结了目前对这类B细胞亚群特征的认识。然后,我们讨论了可能的调节机制的B细胞,并具体定义的作用,调节B细胞在肠道免疫稳态。
B lymphocytes contribute to physiological immunity through organogenesis of secondary lymphoid organs, presentation of antigen to T cells, production of antibodies, and secretion of cytokines. Their role in several autoimmune diseases, mainly as producers of pathogenic antibodies, is also well known. However, certain subsets of B cells are emerging as the important regulatory cell populations in both mouse and human. The regulatory functions of B cells have been demonstrated in a variety of mouse models of autoimmune diseases including collagen-induced arthritis (CIA), experiment autoimmune encephalomyelitis (EAE), anterior chamber-associated immune deviation (ACAID), diabetes, contact hypersensitivity (CHS), and intestinal mucosal inflammation. Accumulating evidence from both mouse and human studies confirms the existence of regulatory B cells, and is beginning to define their mechanisms of action. In this article, we first review the history of B cells with regulatory function in autoimmune diseases, and summarize the current understanding about the characterizations of such B-cell subsets. We then discuss the possible regulatory mechanisms of B cells, and specifically define the role of regulatory B cells in immune homeostasis in the intestine.
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