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重新利用靶向小胶质细胞的免疫调节药物治疗肌萎缩侧索硬化症。

Repurposing immunomodulatory drugs targeting microglia for amyotrophic lateral sclerosis.

作者信息

Hendricus Maes Kirsten Johanna, Briedé Jacco Jan

机构信息

Department of Translational Genomics, Maastricht University, Maastricht, the Netherlands.

Mental Health and Neuroscience Research Institute, Maastricht University, Maastricht, the Netherlands.

出版信息

Brain Res. 2026 Jan 1;1870:150032. doi: 10.1016/j.brainres.2025.150032. Epub 2025 Nov 7.

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder that progressively affects upper and lower motor neurons, leading to symptoms including dysarthria, muscle weakness, and paralysis. The disease is multifactorial, with a variety of contributing pathways, including excitotoxicity, oxidative stress, and neuroinflammation. Current treatments target only two of these pathways with limited efficacy, highlighting the need for alternative approaches. Increasing evidence highlights the involvement of immune dysregulation, particularly microglial-mediated neuroinflammation, in ALS pathology. Fortunately, many immunomodulatory drugs acting on microglia are already available for other diseases, indicating promising opportunities for drug repurposing. This literature review provides an overview of existing drugs under investigation for ALS, including those that have failed, and highlights microglia-targeting compounds with emerging repurposing potential. Compounds such as ibudilast, fingolimod, and modafinil have shown encouraging initial clinical results, whereas others were well-tolerated but underpowered or failed to demonstrate efficacy. New candidates, such as azithromycin, montelukast, doxycycline, tofacitinib, quercetin, belinostat, propranolol, and several kinase inhibitors, have demonstrated positive preclinical results, supporting their advancement toward clinical evaluation. Overall, these findings emphasize the potential of microglia-targeting therapies for ALS. To realize this potential, future studies must include larger cohorts, assess effects across different disease stages and patient subgroups, and examine sex differences. This is essential to address patient heterogeneity and improve personalized treatments for ALS patients.

摘要

肌萎缩侧索硬化症(ALS)是一种致命的神经退行性疾病,会逐渐影响上下运动神经元,导致构音障碍、肌肉无力和瘫痪等症状。该疾病是多因素的,有多种致病途径,包括兴奋性毒性、氧化应激和神经炎症。目前的治疗仅针对其中两条途径,疗效有限,这凸显了需要采用替代方法。越来越多的证据表明免疫失调,特别是小胶质细胞介导的神经炎症,参与了ALS的病理过程。幸运的是,许多作用于小胶质细胞的免疫调节药物已可用于治疗其他疾病,这表明药物重新利用有很大的潜力。这篇文献综述概述了正在研究用于ALS的现有药物,包括那些已失败的药物,并强调了具有新兴重新利用潜力的靶向小胶质细胞的化合物。异丁司特、芬戈莫德和莫达非尼等化合物已显示出令人鼓舞的初步临床结果,而其他一些药物耐受性良好,但效果不佳或未能证明其疗效。新的候选药物,如阿奇霉素、孟鲁司特、多西环素、托法替布、槲皮素、贝利司他、普萘洛尔和几种激酶抑制剂,已在临床前研究中显示出积极结果,支持它们进入临床评估阶段。总体而言,这些发现强调了靶向小胶质细胞疗法对ALS的潜力。为了实现这一潜力,未来的研究必须纳入更大的队列,评估不同疾病阶段和患者亚组的效果,并研究性别差异差异。这对于解决患者异质性和改善ALS患者的个性化治疗至关重要。

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