Popescu Bogdan F Gh, Pirko Istvan, Lucchinetti Claudia F
Department of Neurology, Mayo Clinic College of Medicine, 200 First St Southwest, Rochester, MN 55905, USA.
Continuum (Minneap Minn). 2013 Aug;19(4 Multiple Sclerosis):901-21. doi: 10.1212/01.CON.0000433291.23091.65.
This article summarizes the pathologic features of multiple sclerosis (MS) and other inflammatory demyelinating diseases and discusses neuropathologic studies that have yielded novel insights into potential mechanisms of demyelination.
The pathologic hallmark of MS consists of focal demyelinated plaques within the CNS, with variable degrees of inflammation, gliosis, and neurodegeneration. Active MS lesions show a profound pathologic heterogeneity with four major patterns of immunopathology, suggesting that the targets of injury and mechanisms of demyelination in MS may be different in different disease subgroups. Recent pathologic studies have suggested that the subarachnoid space and cortex may be initial sites and targets of the MS disease process, that inflammatory cortical demyelination is present early in MS, and that meningeal inflammation may drive cortical and white matter injury in some MS patients.
MS is heterogeneous with respect to clinical, genetic, radiographic, and pathologic features; surrogate MRI, clinical, genetic, serologic, and/or CSF markers for each of the four immunopatterns need to be developed in order to recognize them in the general nonbiopsied MS population. Inflammatory cortical demyelination is an important early event in the pathogenesis of MS and may be driven by meningeal inflammation. These observations stress the importance of developing imaging techniques able to capture early inflammatory cortical demyelination in order to better understand the disease pathogenesis and to determine the impact of potential disease-modifying therapies on the cortex.
本文总结了多发性硬化(MS)及其他炎性脱髓鞘疾病的病理特征,并讨论了对脱髓鞘潜在机制有新见解的神经病理学研究。
MS的病理特征是中枢神经系统内出现局灶性脱髓鞘斑块,伴有不同程度的炎症、胶质增生和神经变性。活动性MS病变表现出明显的病理异质性,有四种主要的免疫病理学模式,这表明MS中损伤靶点和脱髓鞘机制在不同疾病亚组中可能不同。最近的病理研究表明,蛛网膜下腔和皮质可能是MS疾病进程的初始部位和靶点,炎性皮质脱髓鞘在MS早期就存在,并且脑膜炎症可能在一些MS患者中驱动皮质和白质损伤。
MS在临床、遗传、影像学和病理特征方面具有异质性;需要开发针对四种免疫模式中每种模式的替代MRI、临床、遗传、血清学和/或脑脊液标志物,以便在一般未进行活检的MS人群中识别它们。炎性皮质脱髓鞘是MS发病机制中的一个重要早期事件,可能由脑膜炎症驱动。这些观察结果强调了开发能够捕捉早期炎性皮质脱髓鞘的成像技术的重要性,以便更好地理解疾病发病机制,并确定潜在疾病修饰疗法对皮质的影响。