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Treatment of multiple sclerosis by transplantation of neural stem cells derived from induced pluripotent stem cells

机译:移植诱导性多能干细胞衍生的神经干细胞治疗多发性硬化症

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Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS), with focal T lymphocytic infiltration and damage of myelin and axons. The underlying mechanism of pathogenesis remains unclear and there are currently no effective treatments. The development of neural stem cell (NSC) transplantation provides a promising strategy to treat neurodegenerative disease. However, the limited availability of NSCs prevents their application in neural disease therapy. In this study, we generated NSCs from induced pluripotent stem cells (iPSCs) and transplanted these cells into mice with experimental autoimmune encephalomyelitis (EAE), a model of MS. The results showed that transplantation of iPSC-derived NSCs dramatically reduced T cell infiltration and ameliorated white matter damage in the treated EAE mice. Correspondingly, the disease symptom score was greatly decreased, and motor ability was dramatically rescued in the iPSC-NSC-treated EAE mice, indicating the effectiveness of using iPSC-NSCs to treat MS. Our study provides pre-clinical evidence to support the feasibility of treating MS by transplantation of iPSC-derived NSCs.
机译:多发性硬化症(MS)是中枢神经系统(CNS)的一种自身免疫性疾病,具有局灶性T淋巴细胞浸润以及髓磷脂和轴突损伤。发病机理的基本机制仍不清楚,目前尚无有效的治疗方法。神经干细胞(NSC)移植的发展为治疗神经退行性疾病提供了一种有希望的策略。然而,NSCs的有限可用性阻止了它们在神经疾病治疗中的应用。在这项研究中,我们从诱导多能干细胞(iPSC)生成了NSC,并将这些细胞移植到患有MS模型的实验性自身免疫性脑脊髓炎(EAE)的小鼠中。结果表明,在治疗后的EAE小鼠中,iPSC衍生的NSC的移植显着减少了T细胞浸润并改善了白质损伤。相应地,在iPSC-NSC治疗的EAE小鼠中,疾病症状评分大大降低,运动能力得到了显着恢复,表明使用iPSC-NSC治疗MS的有效性。我们的研究提供了临床前证据,以支持通过iPSC衍生的NSC移植治疗MS的可行性。

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