进展性多发性硬化症皮质损伤的炎症机制

L. Zuroff, J. Benjamins, A. Bar-Or, R. Lisak
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引用次数: 6

摘要

多发性硬化症(MS)是一种终生炎症性中枢神经系统脱髓鞘疾病。虽然在开发复发性疾病的治疗策略方面取得了实质性进展,但该领域在对疾病进展阶段的理解和管理方面落后,分别包括继发性进行性和原发性进行性多发性硬化症。现在人们认为,不同但暂时重叠的机制是该疾病复发和进展方面的基础。复发性疾病的特征是外周免疫细胞激活和中枢神经系统浸润,导致白质的局灶性破坏,而进行性疾病被认为是由中枢神经系统内的慢性、低度多灶性炎症引起的。具体而言,外周B细胞、T细胞和髓系细胞驻留在发炎的中枢神经系统的小生境中,如软脑膜和Virchow-Robin间隙,其中外周细胞和中枢神经系统驻留细胞之间的复杂相互作用用于维持这些细胞聚集并进一步传播中枢神经系统损伤。特别是,脑膜内的免疫浸润与一种特殊形式的皮质损伤密切相关,称为脑膜下皮质脱髓鞘,这被认为是疾病进展的关键病理驱动因素。多发性硬化症大脑的皮层损伤可能是通过多种免疫介导和退行性过程的结合发生的,可能包括保留在脑膜内的外周免疫细胞产生可扩散的毒性介质。更好地理解外周免疫细胞和中枢神经系统驻留细胞之间的相互作用不仅与我们对疾病过程的概念有关,而且代表了一个更特异于进行性疾病生物学的治疗干预的新靶点。这篇综述将集中在第2页Zuroff等人的作用。Neuroimmunol Neuroinfinition 2020;7:[在线优先]我http://dx.doi.org/10.20517/2347-8659.2020.35多发性硬化症皮层损伤发展过程中的中枢神经系统区隔炎症,特别强调免疫中枢神经系统串扰在疾病进展中的重要性。
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Inflammatory mechanisms underlying cortical injury in progressive multiple sclerosis
Multiple sclerosis (MS) is a lifelong inflammatory demyelinating disease of the central nervous system (CNS). While there has been substantial progress in the development of therapeutic strategies for relapsing disease, the field has lagged behind in its understanding and management of progressive stages of the disease, including secondary progressive and primary progressive MS, respectively. It is now thought that distinct but temporally overlapping mechanisms underlie relapsing and progressive aspects of the disease. Relapsing disease is characterized by waves of peripheral immune cell activation and CNS infiltration leading to focal destruction of the white matter, while progressive disease is thought to be driven by chronic, low-grade multifocal inflammation contained within the CNS compartment. Specifically, peripheral B cells, T cells, and myeloid cells take up residence within niches of the inflamed CNS, such as the leptomeninges and the Virchow-Robin spaces, where complex interactions between peripheral and CNS resident cells serve to maintain these cellular aggregates and further propagate CNS injury. In particular, immune infiltrates within the meninges are tightly associated with a specific form of cortical injury, termed subpial cortical demyelination, which is thought to be a key pathologic driver of disease progression. Cortical injury in the MS brain likely occurs via a combination of multiple immune-mediated and degenerative processes, perhaps including the production of diffusible toxic mediators by peripheral immune cells retained within the meninges. A better understanding of the interplay between peripheral immune and CNS resident cells is not only relevant to our concept of the disease process, but also represents a novel target for therapeutic intervention that is more specific to progressive disease biology. This review will focus on the role of Page 2 Zuroff et al. Neuroimmunol Neuroinflammation 2020;7:[Online First] I http://dx.doi.org/10.20517/2347-8659.2020.35 CNS-compartmentalized inflammation in the development of cortical injury in MS, with a particular emphasis on the importance of immune-CNS crosstalk in disease progression.
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