Luessi Felix, Zipp Frauke, Witsch Esther
Department of Neurology, Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg-University of Mainz,Rhine Main Neuroscience Network (rmn2), Langenbeckstrasse 1, 55131, Mainz, Germany.
Cell Mol Life Sci. 2016 Jul;73(13):2425-50. doi: 10.1007/s00018-016-2170-9. Epub 2016 Mar 12.
Multiple sclerosis (MS) is the most common chronic inflammatory demyelinating disorder of the central nervous system characterized by infiltration of immune cells and progressive damage to myelin sheaths and neurons. There is still no cure for the disease, but drug regimens can reduce the frequency of relapses and slightly delay progression. Myeloid cells or antigen-presenting cells (APCs) such as dendritic cells (DC), macrophages, and resident microglia, are key players in both mediating immune responses and inducing immune tolerance. Mounting evidence indicates a contribution of these myeloid cells to the pathogenesis of multiple sclerosis and to the effects of treatment, the understanding of which might provide strategies for more potent novel therapeutic interventions. Here, we review recent insights into the role of APCs, with specific focus on DCs in the modulation of neuroinflammation in MS.
多发性硬化症(MS)是中枢神经系统最常见的慢性炎性脱髓鞘疾病,其特征为免疫细胞浸润以及髓鞘和神经元的进行性损伤。目前该疾病仍无法治愈,但药物疗法可降低复发频率并略微延缓疾病进展。髓样细胞或抗原呈递细胞(APC),如树突状细胞(DC)、巨噬细胞和常驻小胶质细胞,在介导免疫反应和诱导免疫耐受方面均发挥关键作用。越来越多的证据表明,这些髓样细胞在多发性硬化症的发病机制及治疗效果中发挥作用,对其的了解可能为更有效的新型治疗干预措施提供策略。在此,我们综述了关于抗原呈递细胞作用的最新见解,特别关注树突状细胞在多发性硬化症神经炎症调节中的作用。