Center for Brain Research, Medical University of Vienna, A-1090 Wien, Austria.
Cold Spring Harb Perspect Med. 2018 Mar 1;8(3):a028936. doi: 10.1101/cshperspect.a028936.
Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS), which gives rise to focal lesions in the gray and white matter and to diffuse neurodegeneration in the entire brain. In this review, the spectrum of MS lesions and their relation to the inflammatory process is described. Pathology suggests that inflammation drives tissue injury at all stages of the disease. Focal inflammatory infiltrates in the meninges and the perivascular spaces appear to produce soluble factors, which induce demyelination or neurodegeneration either directly or indirectly through microglia activation. The nature of these soluble factors, which are responsible for demyelinating activity in sera and cerebrospinal fluid of the patients, is currently undefined. Demyelination and neurodegeneration is finally accomplished by oxidative injury and mitochondrial damage leading to a state of "virtual hypoxia."
多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性炎症性脱髓鞘疾病,导致灰质和白质中的局灶性病变以及整个大脑中的弥漫性神经退行性变。在这篇综述中,描述了 MS 病变的范围及其与炎症过程的关系。病理学表明,炎症在疾病的所有阶段都驱动组织损伤。脑膜和血管周围空间中的局灶性炎症浸润似乎产生可溶性因子,这些因子通过小胶质细胞激活直接或间接地诱导脱髓鞘或神经退行性变。这些可溶性因子的性质目前尚不清楚,它们负责患者血清和脑脊液中的脱髓鞘活性。脱髓鞘和神经退行性变最终通过氧化损伤和线粒体损伤导致“虚拟缺氧”状态。