Rodgers Jane M, Robinson Andrew P, Miller Stephen D
Department of Microbiology-Immunology and Interdepartmental Immunobiology Center, Northwestern University Feinberg School of Medicine, 303 E. Chicago Ave., Chicago, Illinois 60611, USA.
Discov Med. 2013 Aug;16(86):53-63.
Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) characterized by encephalitogenic leukocyte infiltration and multifocal plaques of demyelination. Patients present with debilitating clinical sequelae including motor, sensory, and cognitive deficits. For the past 30 years, immune modulating treatments have entered the marketplace and continue to improve in limiting the frequency and severity of relapses, but no cure has been found and no drug has successfully stopped chronic progressive disease. Recent work focusing on the oligodendrocyte, the myelin-producing cell, has provided needed insight into the process of demyelination, the spontaneous ability of the CNS to regenerate, and the inevitable failure of remyelination. From this a number of promising molecular targets have been identified to protect oligodendrocytes and promote remyelination. Combining immunomodulatory therapy with strategies to protect oligodendrocytes from further degeneration and enhance remyelination presents a very real means to improve clinical outcome for chronic progressive patients in the near future. Here we lay out a combination therapy approach to treating MS and survey the current literature on promising drug candidates potentially capable of mediating oligodendrocyte protection and enhancing remyelination.
多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性炎症性脱髓鞘疾病,其特征为致脑炎性白细胞浸润和多灶性脱髓鞘斑块。患者会出现使人衰弱的临床后遗症,包括运动、感觉和认知缺陷。在过去30年里,免疫调节治疗已进入市场,并且在限制复发频率和严重程度方面持续改善,但尚未找到治愈方法,也没有药物成功阻止慢性进行性疾病。最近针对少突胶质细胞(产生髓磷脂的细胞)的研究工作,为脱髓鞘过程、CNS的自发再生能力以及髓鞘再生的必然失败提供了必要的见解。由此确定了一些有前景的分子靶点,以保护少突胶质细胞并促进髓鞘再生。将免疫调节疗法与保护少突胶质细胞免于进一步退化并增强髓鞘再生的策略相结合,是在不久的将来改善慢性进行性患者临床结局的一种切实可行的方法。在此,我们阐述一种治疗MS的联合治疗方法,并综述当前有关可能能够介导少突胶质细胞保护和增强髓鞘再生的有前景候选药物的文献。