Department of Immunology and Microbiology, Shanghai JiaoTong University School of Medicine, Shanghai Institute of Immunology, Shanghai 200025, China.
Mediators Inflamm. 2014;2014:659206. doi: 10.1155/2014/659206. Epub 2014 Jan 2.
Multiple sclerosis is an autoimmune disease with classical traits of demyelination, axonal damage, and neurodegeneration. The migration of autoimmune T cells and macrophages from blood to central nervous system as well as the destruction of blood brain barrier are thought to be the major processes in the development of this disease. Chemokines, which are small peptide mediators, can attract pathogenic cells to the sites of inflammation. Each helper T cell subset expresses different chemokine receptors so as to exert their different functions in the pathogenesis of MS. Recently published results have shown that the levels of some chemokines and chemokine receptors are increased in blood and cerebrospinal fluid of MS patients. This review describes the advanced researches on the role of chemokines and chemokine receptors in the development of MS and discusses the potential therapy of this disease targeting the chemokine network.
多发性硬化症是一种自身免疫性疾病,具有脱髓鞘、轴突损伤和神经退行性病变的典型特征。自身免疫性 T 细胞和巨噬细胞从血液向中枢神经系统的迁移以及血脑屏障的破坏被认为是这种疾病发展的主要过程。趋化因子是小分子肽介质,可以吸引致病细胞到炎症部位。每种辅助性 T 细胞亚群表达不同的趋化因子受体,以便在 MS 的发病机制中发挥不同的功能。最近发表的结果表明,多发性硬化症患者的血液和脑脊液中某些趋化因子和趋化因子受体的水平升高。本文综述了趋化因子及其受体在多发性硬化症发病机制中的作用的研究进展,并讨论了针对趋化因子网络的这种疾病的潜在治疗方法。