Treg细胞的B细胞对应物:作为自身免疫性疾病治疗的新靶点

Myong-Guk Ri, Cholho Kang
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引用次数: 0

摘要

B细胞通过产生抗体和向T细胞呈递抗原而被认为是一种积极的免疫调节剂。最近,研究表明B细胞包含罕见但有效的亚群,能够通过多种调节机制抑制免疫反应。B细胞的这一部分,被称为调节性B细胞(Bregs),负调节免疫反应并有助于免疫耐受。在几个调节性B细胞亚群中,产生白细胞介素10 (IL-10)的调节性B细胞被广泛研究。对实验动物模型以及自身免疫性疾病患者的研究已经确定Breg亚群对严重免疫疾病表现出强大的治疗工具。现在,人类调节性B细胞正在成为一个活跃的研究领域。了解调节性B细胞的全貌需要明确的标准来识别这些细胞亚群及其生理特征背后的关键分子机制。本文综述了目前对调节性B细胞的认识,主要是产生il -10的调节性B细胞。
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B cell counterpart of Treg cells: As a new target for autoimmune disease therapy
B cells have been considered a positive immune regulator by producing antibodies and presenting antigens to T cells. Recently, it has been shown that B cells comprise rare but potent subset capable of inhibiting immune responses via diverse regulatory mechanisms. This subset of B cells, known as regulatory B cells (Bregs), negatively regulates immune responses and contributes to immune tolerance. Among several regulatory B cell subsets, interleukin 10 (IL-10)-producing regulatory B cells are intensively investigated. Studies in experimental animal models, as well as in patients with autoimmune diseases, have identified Breg subsets exhibiting a powerful therapeutic tool for severe immune disorders. Now, human regulatory B cells are becoming an active area of research. Clear criteria to identify these cell subsets and the key molecular mechanisms underlying their physiological features are required for understanding the complete picture of regulatory B cells. This review highlights the current knowledge on regulatory B cells, mainly IL-10-producing regulatory B cells.
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