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多发性硬化症中少突胶质细胞和髓鞘的病理生理学

Oligodendrocyte and Myelin Pathophysiology in Multiple Sclerosis.

作者信息

López-Muguruza Eneritz, Peiró-Moreno Carla, Ruiz Asier, Matute Carlos

机构信息

Department of Neurosciences, University of the Basque Country UPV/EHU, IIS-BioBizkaia and CIBERNED, Leioa, Spain.

Achucarro Basque Centre for Neuroscience, Leioa, Spain.

出版信息

Adv Neurobiol. 2025;43:317-361. doi: 10.1007/978-3-031-87919-7_12.

Abstract

Multiple sclerosis (MS) is a chronic autoimmune and progressive neurodegenerative disease of the central nervous system (CNS) that has a highly variable clinical manifestation and course. MS targets primarily myelin and oligodendroglia; however, all glial cells and neurons become involved early in the pathology. Thus, inflammation, which is widely thought to be initiated peripherally, expands through the CNS, with astrocytes and microglia entering an activated state not only around and within lesions but also widespread. This chapter will emphasize the pathophysiological changes in oligodendrocytes and myelin as a consequence of the inflammatory cascade driving the disease onset and progression. Learning about the mechanisms of oligodendrocyte and myelin damage beyond the immune attack will be instrumental in protecting these two CNS compartments from damage. In turn, knowledge about the axon-myelin unit will help in devising therapies to prevent axonal degeneration, a key clinical hallmark of MS, as it strongly correlates with the progression of CNS atrophy and symptoms. Finally, exploiting paradigms of oligodendrocyte repopulation and remyelination will definitively contribute to devising treatments for tissue repair and halting MS course. This chapter aims at summarizing the state of the art in all these experimental developments including the available clinical therapies and the current clinical trials.

摘要

多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性自身免疫性和进行性神经退行性疾病,其临床表现和病程具有高度变异性。MS主要靶向髓鞘和少突胶质细胞;然而,在病理过程早期,所有神经胶质细胞和神经元都会受累。因此,炎症虽普遍被认为始于外周,但会在中枢神经系统中扩散,星形胶质细胞和小胶质细胞不仅在病变周围和内部,而且在全身都会进入激活状态。本章将重点阐述炎症级联反应驱动疾病发生和发展过程中少突胶质细胞和髓鞘的病理生理变化。了解免疫攻击之外的少突胶质细胞和髓鞘损伤机制,将有助于保护这两个中枢神经系统组成部分免受损伤。反过来,关于轴突 - 髓鞘单元的知识将有助于设计预防轴突变性的疗法,轴突变性是MS的一个关键临床特征,因为它与中枢神经系统萎缩和症状的进展密切相关。最后,利用少突胶质细胞再填充和髓鞘再生的范例,将最终有助于设计组织修复和阻止MS病程的治疗方法。本章旨在总结所有这些实验进展的现状,包括现有的临床疗法和当前的临床试验。

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