Department of Neurology, Medical University of Vienna, Vienna, Austria.
Department of Neurology, Barzilai University Medical Center, Ashkelon, Israel.
Front Immunol. 2019 Jul 11;10:1564. doi: 10.3389/fimmu.2019.01564. eCollection 2019.
Multiple sclerosis (MS) is the most common neurological immune-mediated disease leading to disability in young adults. The outcome of the disease is unpredictable, and over time, neurological disabilities accumulate. Interferon beta-1b was the first drug to be approved in the 1990s for relapsing-remitting MS to modulate the course of the disease. Over the past two decades, the treatment landscape has changed tremendously. Currently, more than a dozen drugs representing 1 substances with different mechanisms of action have been approved (interferon beta preparations, glatiramer acetate, fingolimod, siponimod, mitoxantrone, teriflunomide, dimethyl fumarate, cladribine, alemtuzumab, ocrelizumab, and natalizumab). Ocrelizumab was the first medication to be approved for primary progressive MS. The objective of this review is to present the modes of action of these drugs and their effects on the immunopathogenesis of MS. Each agent's clinical development and potential side effects are discussed.
多发性硬化症(MS)是最常见的导致年轻人残疾的神经免疫介导性疾病。该疾病的预后不可预测,而且随着时间的推移,神经功能障碍会逐渐累积。干扰素β-1b 是 20 世纪 90 年代批准的第一种用于治疗复发缓解型多发性硬化症的药物,可调节疾病进程。在过去的二十年中,治疗方法发生了巨大的变化。目前,已有十几种药物(包括干扰素β制剂、那他珠单抗、奥瑞珠单抗、替西罗莫司、西尼莫德、芬戈莫德、甲氨蝶呤、米托蒽醌、特立氟胺、阿仑单抗、奥瑞珠单抗和那他珠单抗)获得批准,代表了 1 种作用机制不同的物质。奥瑞珠单抗是第一种被批准用于原发性进展型多发性硬化症的药物。本文旨在介绍这些药物的作用模式及其对多发性硬化症免疫发病机制的影响。讨论了每种药物的临床开发和潜在的副作用。