多发性硬化
免疫系统
背景(考古学)
实验性自身免疫性脑脊髓炎
医学
神经退行性变
免疫学
疾病
中枢神经系统
血脑屏障
神经科学
细胞疗法
调节性T细胞
T细胞
干细胞
生物
病理
白细胞介素2受体
古生物学
遗传学
作者
Janne Verreycken,Paulien Baeten,Bieke Broux
标识
DOI:10.1080/21645515.2022.2153534
摘要
Multiple sclerosis (MS) is an autoimmune disorder causing demyelination and neurodegeneration in the central nervous system. MS is characterized by disturbed motor performance and cognitive impairment. Current MS treatments delay disease progression and reduce relapse rates with general immunomodulation, yet curative therapies are still lacking. Regulatory T cells (Tregs) are able to suppress autoreactive immune cells, which drive MS pathology. However, Tregs are functionally impaired in people with MS. Interestingly, Tregs were recently reported to also have regenerative capacity. Therefore, experts agree that Treg cell therapy has the potential to ameliorate the disease. However, to perform their local anti-inflammatory and regenerative functions in the brain, they must first migrate across the blood-brain barrier (BBB). This review summarizes the reported results concerning the migration of Tregs across the BBB and the influence of Tregs on migration of other immune subsets. Finally, their therapeutic potential is discussed in the context of MS.
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