Stys Peter K, Tsutsui Shigeki, Gafson Arie R, 't Hart Bert A, Belachew Shibeshih, Geurts Jeroen J G
Department of Clinical Neurosciences, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Biogen Digital Health, Biogen, Cambridge, MA, United States.
Front Cell Neurosci. 2024 Aug 5;18:1426231. doi: 10.3389/fncel.2024.1426231. eCollection 2024.
Multiple sclerosis (MS) is a frequently disabling neurological disorder characterized by symptoms, clinical signs and imaging abnormalities that typically fluctuate over time, affecting any level of the CNS. Prominent lymphocytic inflammation, many genetic susceptibility variants involving immune pathways, as well as potent responses of the neuroinflammatory component to immunomodulating drugs, have led to the natural conclusion that this disease is driven by a primary autoimmune process. In this Hypothesis and Theory article, we discuss emerging data that cast doubt on this assumption. After three decades of therapeutic experience, what has become clear is that potent immune modulators are highly effective at suppressing inflammatory relapses, yet exhibit very limited effects on the later progressive phase of MS. Moreover, neuropathological examination of MS tissue indicates that degeneration, CNS atrophy, and myelin loss are most prominent in the progressive stage, when lymphocytic inflammation paradoxically wanes. Finally, emerging clinical observations such as "progression independent of relapse activity" and "silent progression," now thought to take hold very early in the course, together argue that an underlying "cytodegenerative" process, likely targeting the myelinating unit, may in fact represent the most proximal step in a complex pathophysiological cascade exacerbated by an autoimmune inflammatory overlay. Parallels are drawn with more traditional neurodegenerative disorders, where a progressive proteopathy with prion-like propagation of toxic misfolded species is now known to play a key role. A potentially pivotal contribution of the Epstein-Barr virus and B cells in this process is also discussed.
多发性硬化症(MS)是一种常导致残疾的神经系统疾病,其特征为症状、临床体征和影像学异常,这些通常会随时间波动,影响中枢神经系统(CNS)的任何水平。显著的淋巴细胞炎症、许多涉及免疫途径的遗传易感性变异,以及神经炎症成分对免疫调节药物的强烈反应,自然而然地得出结论,即这种疾病是由原发性自身免疫过程驱动的。在这篇假说与理论文章中,我们讨论了对这一假设提出质疑的新数据。经过三十年的治疗经验,现在已经明确的是,强效免疫调节剂在抑制炎症复发方面非常有效,但对MS的后期进展阶段影响非常有限。此外,对MS组织的神经病理学检查表明,在进展期,当淋巴细胞炎症反而减弱时,变性、CNS萎缩和髓鞘丢失最为明显。最后,诸如“与复发活动无关的进展”和“无症状进展”等新出现的临床观察结果,现在认为在病程早期就已出现,共同表明一个潜在的“细胞变性”过程,可能以髓鞘形成单位为靶点,实际上可能是由自身免疫性炎症叠加加剧的复杂病理生理级联反应中最接近的一步。文中将其与更传统的神经退行性疾病进行了比较,在这些疾病中,一种具有毒性错误折叠物种的朊病毒样传播的进行性蛋白质病现在已知起着关键作用。还讨论了爱泼斯坦 - 巴尔病毒和B细胞在这一过程中可能的关键作用。