Yong V Wee
Department of Oncology and Clinical Neurosciences, University of Calgary, Alberta, Canada.
Neurology. 2002 Sep 24;59(6):802-8. doi: 10.1212/wnl.59.6.802.
Interferon-beta and glatiramer acetate (GA) are the two main groups of drugs used in the treatment of MS. Notably, while both ultimately decrease CNS inflammation, they do so by very different mechanisms. Interferon-beta has potent activity at the blood-brain barrier and impairs the trafficking of inflammatory cells into the CNS. In contrast, GA has negligible effect at the blood-brain barrier, allowing GA-specific T helper 2 lymphocytes to enter the CNS to decrease inflammation through bystander suppression. Other differences are also emphasized. The presence of GA-reactive lymphocytes within the CNS parenchyma may have the additional benefit of conferring neuroprotection through protective autoimmunity.
β-干扰素和醋酸格拉替雷(GA)是用于治疗多发性硬化症(MS)的两大类主要药物。值得注意的是,虽然两者最终都能减轻中枢神经系统炎症,但它们的作用机制截然不同。β-干扰素在血脑屏障处具有强大活性,会损害炎性细胞进入中枢神经系统的运输过程。相比之下,GA在血脑屏障处的作用可忽略不计,使得GA特异性辅助性T细胞2淋巴细胞能够进入中枢神经系统,通过旁观者抑制作用减轻炎症。其他差异也得到了强调。中枢神经实质内存在GA反应性淋巴细胞可能还具有通过保护性自身免疫提供神经保护的额外益处。