Aharoni Rina
a Department of Immunology , The Weizmann Institute of Science , Rehovot , Israel.
Expert Rev Neurother. 2015;15(12):1369-72. doi: 10.1586/14737175.2015.1112740. Epub 2015 Nov 11.
Multiple sclerosis (MS) is a multifaceted disease, in which an inflammatory autoimmune attack on the myelin in the central nervous system (CNS) leads to extensive demyelination and subsequent axonal pathology. The challenge for MS therapy is to combine effective immunomodulatory therapies with novel neuroprotective approaches that promote repair, in particular remyelination, beyond its limited spontaneous extent. Cumulative findings indicate that immunomodulatory treatments can induce neuroprotective outcomes and provide a supportive milieu for repair processes. Growing understanding of MS pathology together with biotechnological advances has resulted in promising strategies such as inhibitory molecules, monoclonal antibodies and cell therapies. Several candidates that have shown significant effects on the oligodendrocyte population and/or myelin synthesis in animal models are currently or soon to be tested in clinical trials.
多发性硬化症(MS)是一种多方面的疾病,其中针对中枢神经系统(CNS)髓鞘的炎症性自身免疫攻击会导致广泛的脱髓鞘以及随后的轴突病变。MS治疗面临的挑战是将有效的免疫调节疗法与促进修复(特别是髓鞘再生,超越其有限的自发程度)的新型神经保护方法相结合。累积的研究结果表明,免疫调节治疗可以诱导神经保护作用,并为修复过程提供支持性环境。对MS病理学的深入了解以及生物技术的进步催生了一些有前景的策略,如抑制性分子、单克隆抗体和细胞疗法。目前或即将在临床试验中测试几种在动物模型中对少突胶质细胞群体和/或髓鞘合成显示出显著效果的候选药物。