再髓鞘化
多发性硬化
医学
神经退行性变
免疫抑制
中枢神经系统
再生(生物学)
实验性自身免疫性脑脊髓炎
胶质增生
脱髓鞘病
神经保护
疾病
免疫学
病理
内科学
生物
髓鞘
细胞生物学
作者
Sayyed Ourmazd Mohseni,Kin Man Au,Wadih Issa,Lifu Ruan,Olaf Stüve,Andrew Z. Wang
出处
期刊:Biomaterials
[Elsevier]
日期:2024-09-03
卷期号:313: 122807-122807
标识
DOI:10.1016/j.biomaterials.2024.122807
摘要
Multiple Sclerosis (MS) is an autoimmune condition targeting the central nervous system (CNS) characterized by focal demyelination with inflammation, causing neurodegeneration and gliosis. This is accompanied by a refractory period in relapsing MS or chronic progression in primary progressive MS. Current MS treatments target disease relapses and aim to reduce further demyelination and disability. These include the treatment of acute exacerbations through global immunomodulation upon corticosteroid administration, which are accompanied by adverse reactions. Disease modifying therapies (DMTs) which provide targeted immunosuppression of T and B cells, and sequestration of leukocytes out of CNS, have led to further improvements in demyelination prevention and disease burden reduction. Despite their efficacy, DMTs are ineffective in remyelination, pathology reversal and have minimal effects in progressive MS. The advent of modern biomedical engineering approaches in combination with a better understanding of MS pathology, has led to the development of novel, regenerative approaches to treatment. Such treatments utilize neural stem cells (NSCs) and can reduce disease relapses and reverse damage caused by the disease through localized tissue regeneration. While at initial stages, pre-clinical and clinical studies utilizing NSCs and immune modulation have shown promising outcomes in tissue regeneration, creating a potential new era in MS therapy.
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