Multiple Sclerosis Center, S Camillo-Forlanini, Neurosciences , Circonvallazione Gianicolense 87, Rome 00152 , Italy
Expert Opin Investig Drugs. 2013 Oct;22(10):1243-53. doi: 10.1517/13543784.2013.820275. Epub 2013 Jul 16.
Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS), traditionally considered to be an autoimmune disease. Despite the standard of care for patients with MS is significantly improved in recent years, there is still room for improvement in terms of effectiveness and also compliance.
The continuous improvements of our understanding of the pathophysiological changes that occur in MS have translated into many novel therapeutic agents at different stages of development. A number of therapies for MS are in advanced development and likely to be available soon. Along with these, we have also seen the appearance of a group of drugs considered together as a consequence of their similar design: the monoclonal antibodies (mAbs). Here, the focus will be on reviewing results that have emerged from a better clarification of MS pathogenesis to clinical trials of different anti-CD20 mAbs.
The decision to switch established patients from well-known drugs to either new formulations or new agents will be made on balancing efficacy and tolerability of the existing treatments. Safety seems increasingly likely to become a key factor.
多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性炎症性疾病,传统上被认为是一种自身免疫性疾病。尽管近年来 MS 患者的标准治疗方法有了显著改善,但在疗效和依从性方面仍有改进的空间。
我们对 MS 发生的病理生理变化的理解不断提高,这转化为许多处于不同开发阶段的新型治疗药物。许多 MS 治疗方法正在深入开发,很快就会上市。除此之外,我们还看到了一组被认为是由于其相似设计而出现的药物:单克隆抗体(mAbs)。在这里,重点将放在从 MS 发病机制的更好阐明到不同抗 CD20 mAbs 的临床试验的结果综述上。
将已确立的患者从知名药物转换为新配方或新药物的决定将基于权衡现有治疗方法的疗效和耐受性。安全性似乎越来越有可能成为一个关键因素。