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Neurodegeneration in multiple sclerosis involves multiple pathogenic mechanisms

机译:多发性硬化症中的神经变性涉及多种致病机制

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摘要

Multiple sclerosis (MS) is a complex autoimmune disease that impairs the central nervous system (CNS). The neurological disability and clinical course of the disease is highly variable and unpredictable from one patient to another. The cause of MS is still unknown, but it is thought to occur in genetically susceptible individuals who develop disease due to a nongenetic trigger, such as altered metabolism, a virus, or other environmental factors. MS patients develop progressive, irreversible, neurological disability associated with neuronal and axonal damage, collectively known as neurodegeneration. Neurodegeneration was traditionally considered as a secondary phenomenon to inflammation and demyelination. However, recent data indicate that neurodegeneration develops along with inflammation and demyelination. Thus, MS is increasingly recognized as a neurodegenerative disease triggered by an inflammatory attack of the CNS. While both inflammation and demyelination are well described and understood cellular processes, neurodegeneration might be defined by a diverse pool of any of the following: neuronal cell death, apoptosis, necrosis, and virtual hypoxia. In this review, we present multiple theories and supporting evidence that identify common biological processes that contribute to neurodegeneration in MS.
机译:多发性硬化症(MS)是一种复杂的自身免疫性疾病,会损害中枢神经系统(CNS)。该疾病的神经系统残疾和临床病程变化很大,一个病人到另一个病人无法预测。 MS的原因仍然未知,但是据认为它发生在由于非遗传触发因素(例如代谢改变,病毒或其他环境因素)而患病的遗传易感人群中。 MS患者发展为与神经元和轴突损伤相关的进行性,不可逆性神经失能,统称为神经变性。传统上,神经变性被认为是炎症和脱髓鞘的继发现象。然而,最近的数据表明神经变性与炎症和脱髓鞘一起发展。因此,越来越多地将MS识别为由CNS的炎性发作触发的神经退行性疾病。虽然炎症和脱髓鞘均已很好地描述和理解了细胞过程,但神经变性可能由以下任何一种的多样性集合定义:神经元细胞死亡,凋亡,坏死和虚拟缺氧。在这篇综述中,我们提出了多种理论和支持性证据,它们确定了导致MS神经变性的常见生物学过程。

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