Neuroimmunology Discovery Performance Unit, GlaxoSmithKline Research and Development Center, Shanghai, China.
Neurosci Bull. 2013 Apr;29(2):144-54. doi: 10.1007/s12264-013-1317-z. Epub 2013 Apr 5.
Multiple sclerosis (MS) is a chronic and devastating autoimmune demyelinating disease of the central nervous system. With the increased understanding of the pathophysiology of this disease in the past two decades, many disease-modifying therapies that primarily target adaptive immunity have been shown to prevent exacerbations and new lesions in patients with relapsing-remitting MS. However, these therapies only have limited efficacy on the progression of disability. Increasing evidence has pointed to innate immunity, axonal damage and neuronal loss as important contributors to disease progression. Remyelination of denuded axons is considered an effective way to protect neurons from damage and to restore neuronal function. The identification of several key molecules and pathways controlling the differentiation of oligodendrocyte progenitor cells and myelination has yielded clues for the development of drug candidates that directly target remyelination and neuroprotection. The long-term efficacy of this strategy remains to be evaluated in clinical trials. Here, we provide an overview of current and emerging therapeutic concepts, with a focus on the opportunities and challenges for the remyelination approach to the treatment of MS.
多发性硬化症(MS)是一种慢性且破坏性的中枢神经系统自身免疫性脱髓鞘疾病。在过去的二十年中,随着对这种疾病病理生理学的深入了解,许多主要针对适应性免疫的疾病修正治疗方法已被证明可预防复发缓解型 MS 患者的恶化和新病变。然而,这些治疗方法对残疾进展的疗效有限。越来越多的证据表明,固有免疫、轴突损伤和神经元丢失是疾病进展的重要因素。裸露轴突的髓鞘再生被认为是保护神经元免受损伤和恢复神经元功能的有效方法。鉴定出控制少突胶质前体细胞分化和髓鞘形成的几个关键分子和途径,为开发直接针对髓鞘再生和神经保护的药物候选物提供了线索。这一策略的长期疗效仍需在临床试验中进行评估。在这里,我们概述了当前和新兴的治疗概念,重点介绍了髓鞘再生方法治疗 MS 的机会和挑战。