Mirshafiey Abbas, Asghari Babak, Ghalamfarsa Ghasem, Jadidi-Niaragh Farhad, Azizi Gholamreza
Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran;
Antimicrobial Resistance Research Center, Faculty of Medicine, Iran University of Medical Science, Tehran, Iran;
Sultan Qaboos Univ Med J. 2014 Feb;14(1):e13-25. doi: 10.12816/0003332. Epub 2014 Jan 27.
Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS). The major pathological outcomes of the disease are the loss of blood-brain barrier (BBB) integrity and the development of reactive astrogliosis and MS plaque. For the disease to occur, the non-resident cells must enter into the immune-privileged CNS through a breach in the relatively impermeable BBB. It has been demonstrated that matrix metalloproteinases (MMPs) play an important role in the immunopathogenesis of MS, in part through the disruption of the BBB and the recruitment of inflammatory cells into the CNS. Moreover, MMPs can also enhance the cleavage of myelin basic protein (MBP) and the demyelination process. Regarding the growing data on the roles of MMPs and their tissue inhibitors (TIMPs) in the pathogenesis of MS, this review discusses the role of different types of MMPs, including MMP-2, -3, -7, -9, -12 and -25, in the immunopathogenesis and treatment of MS.
多发性硬化症(MS)是一种中枢神经系统(CNS)的自身免疫性疾病。该疾病的主要病理结果是血脑屏障(BBB)完整性丧失以及反应性星形胶质细胞增生和MS斑块的形成。为了使疾病发生,非驻留细胞必须通过相对不可渗透的血脑屏障的破损进入免疫特权的中枢神经系统。已经证明,基质金属蛋白酶(MMPs)在MS的免疫发病机制中起重要作用,部分是通过破坏血脑屏障以及将炎症细胞募集到中枢神经系统中。此外,MMPs还可以增强髓鞘碱性蛋白(MBP)的裂解和脱髓鞘过程。鉴于关于MMPs及其组织抑制剂(TIMPs)在MS发病机制中的作用的越来越多的数据,本综述讨论了不同类型的MMPs,包括MMP-2、-3、-7、-9、-12和-25,在MS免疫发病机制和治疗中的作用。