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Effector and regulatory B cells in Multiple Sclerosis

机译:多发性硬化症中的效应和调节B细胞

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摘要

Abstract The role of B cells in the pathogenesis of Multiple Sclerosis (MS), an autoimmune neurodegenerative disease, is becoming eminent in recent years, but the specific contribution of the distinct B cell subsets remains to be elucidated. Several B cell subsets have shown regulatory, anti-inflammatory capacities in response to stimuli in vitro , as well as in the animal model of MS: Experimental Autoimmune Encephalomyelitis (EAE). However, the functional role of the B regulatory cells (Bregs) in vivo and specifically in the human disease is yet to be clarified. In the present review, we have summarized the updated information on the roles of effector and regulatory B cells in MS and the immune-modulatory effects of MS therapeutic agents on their phenotype and function. Highlights ? Altered functions of effector and regulatory B cells are part of MS pathogenesis. ? Environmental stimuli seem to affect MS activity implicating B cell regulation. ? Current MS therapies appear to modulate B cell subset proportions and functions. ? Future immunotherapies for MS might rely on subset-specific B-cell-targeting.
机译:摘要B细胞在多发性硬化症(MS)发病机制中,自身免疫性神经退行性疾病的发病机制,近年来正在成为杰出的,但不同的B细胞子集的具体贡献仍然被阐明。几个B细胞亚群响应于体外刺激的调节,抗炎能力,以及MS的动物模型:实验性自身免疫脑脊髓炎(EAE)。然而,尚未澄清体内B调节细胞(BREG)和特异性在人类疾病中的功能作用。在本综述中,我们总结了关于效应和调节B细胞的作用和MS治疗剂对其表型和功能的免疫调节作用的更新信息。强调 ?效应和调节B细胞的改变功能是MS发病机制的一部分。还环境刺激似乎影响MS活动暗示B细胞调节。还当前的MS疗法似乎调制B小区子集比例和功能。还MS的未来免疫疗法可能依赖于特定的特定B细胞靶向。

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