MS Research Center, Neuroscience Institute, Tehran University of Medical Science, Department of Neurology, Sina Hospital, 1136746911 Tehran, Iran.
Institute of Neuropathology, University Medical Center, D-37075 Göttingen, Germany.
Rev Neurosci. 2018 Dec 19;30(1):67-83. doi: 10.1515/revneuro-2018-0002.
Traditionally, multiple sclerosis (MS) was considered to be a CD4 T cell-mediated CNS autoimmunity, compatible with experimental autoimmune encephalitis model, which can be characterized by focal lesions in the white matter. However, studies of recent decades revealed several missing pieces of MS puzzle and showed that MS pathogenesis is more complex than the traditional view and may include the following: a primary degenerative process (e.g. oligodendroglial pathology), generalized abnormality of normal-appearing brain tissue, pronounced gray matter pathology, involvement of innate immunity, and CD8 T cells and B cells. Here, we review these findings and discuss their implications in MS pathogenesis.
传统上,多发性硬化症(MS)被认为是一种 CD4 T 细胞介导的中枢神经系统自身免疫,与实验性自身免疫性脑炎模型相兼容,其特征是白质中的局灶性病变。然而,近几十年来的研究揭示了多发性硬化症之谜的几个缺失部分,并表明多发性硬化症的发病机制比传统观点更为复杂,可能包括以下几个方面:原发性退行性过程(例如少突胶质病理)、正常外观脑组织的普遍异常、明显的灰质病理、固有免疫、CD8 T 细胞和 B 细胞的参与。在这里,我们回顾这些发现,并讨论它们对多发性硬化症发病机制的影响。