Pröbstel Anne-Katrin, Sanderson Nicholas S R, Derfuss Tobias
Department of Neurology, University Hospital Basel, Petersgraben 4 & Clinical Neuroimmunology, Hebelstrasse 20, 4031 Basel, Switzerland.
Department of Biomedicine, University of Basel, Hebelstrasse 20, 4031 Basel, Switzerland.
Int J Mol Sci. 2015 Jul 21;16(7):16576-92. doi: 10.3390/ijms160716576.
While over the past decades T cells have been considered key players in the pathogenesis of multiple sclerosis (MS), it has only recently become evident that B cells have a major contributing role. Our understanding of the role of B cells has evolved substantially following the clinical success of B cell-targeting therapies and increasing experimental evidence for significant B cell involvement. Rather than mere antibody-producing cells, it is becoming clear that they are team players with the capacity to prime and regulate T cells, and function both as pro- and anti-inflammatory mediators. However, despite tremendous efforts, the target antigen(s) of B cells in MS have yet to be identified. The first part of this review summarizes the clinical evidence and results from animal studies pointing to the relevance of B cells in the pathogenesis of MS. The second part gives an overview of the currently known potential autoantigen targets. The third part recapitulates and critically appraises the currently available B cell-directed therapies.
在过去几十年里,T细胞一直被认为是多发性硬化症(MS)发病机制中的关键因素,但直到最近才明显发现B细胞也起着主要作用。随着针对B细胞疗法在临床上取得成功以及越来越多实验证据表明B细胞大量参与其中,我们对B细胞作用的理解有了很大进展。B细胞已不再仅仅被视为产生抗体的细胞,它们显然是能够启动和调节T细胞的协同参与者,兼具促炎和抗炎介质的功能。然而,尽管付出了巨大努力,MS中B细胞的靶抗原仍未被确定。本综述的第一部分总结了临床证据以及动物研究结果,这些都表明B细胞在MS发病机制中的相关性。第二部分概述了目前已知的潜在自身抗原靶点。第三部分总结并批判性地评估了目前可用的针对B细胞的疗法。