多发性硬化
可药性
神经退行性变
神经科学
免疫系统
医学
实验性自身免疫性脑脊髓炎
再髓鞘化
疾病
中枢神经系统
神经炎症
生物信息学
炎症
生物
免疫学
髓鞘
病理
生物化学
基因
作者
Aakanksha Dixit,Hannah Savage,Judith M. Greer
标识
DOI:10.1080/14728222.2023.2236301
摘要
Multiple sclerosis (MS) is a chronic inflammatory, demyelinating, and neurodegenerative condition affecting the central nervous system (CNS). Although therapeutic approaches have become available over the last 20 years that markedly slow the progression of disease, there is no cure for MS. Furthermore, the capacity to repair existing CNS damage caused by MS remains very limited.Several animal models are widely used in MS research to identify potential druggable targets for new treatment of MS. In this review, we look at targets identified since 2019 in studies using these models, and their potential for effecting a cure for MS.Refinement of therapeutic strategies targeting key molecules involved in the activation of immune cells, cytokine, and chemokine signaling, and the polarization of the immune response have dominated recent publications. While some progress has been made in identifying effective targets to combat chronic demyelination and neurodegeneration, much more work is required. Progress is largely limited by the gaps in knowledge of how the immune system and the nervous system interact in MS and its animal models, and whether the numerous targets present in both systems respond in the same way in each system to the same therapeutic manipulation.
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