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间充质干细胞和诱导多能干细胞作为治疗多发性硬化症的方法。

Mesenchymal stem cells and induced pluripotent stem cells as therapies for multiple sclerosis.

作者信息

Xiao Juan, Yang Rongbing, Biswas Sangita, Qin Xin, Zhang Min, Deng Wenbin

机构信息

Medical College, Hubei University of Arts and Science, Xiangyang 441053, China.

Department of Biological Treatment, Handan Central Hospital, Handan 056001, China.

出版信息

Int J Mol Sci. 2015 Apr 24;16(5):9283-302. doi: 10.3390/ijms16059283.

Abstract

Multiple sclerosis (MS) is a chronic, autoimmune, inflammatory demyelinating disorder of the central nervous system that leads to permanent neurological deficits. Current MS treatment regimens are insufficient to treat the irreversible neurological disabilities. Tremendous progress in the experimental and clinical applications of cell-based therapies has recognized stem cells as potential candidates for regenerative therapy for many neurodegenerative disorders including MS. Mesenchymal stem cells (MSC) and induced pluripotent stem cell (iPSCs) derived precursor cells can modulate the autoimmune response in the central nervous system (CNS) and promote endogenous remyelination and repair process in animal models. This review highlights studies involving the immunomodulatory and regenerative effects of mesenchymal stem cells and iPSCs derived cells in animal models, and their translation into immunomodulatory and neuroregenerative treatment strategies for MS.

摘要

多发性硬化症(MS)是一种慢性自身免疫性炎症性中枢神经系统脱髓鞘疾病,可导致永久性神经功能缺损。目前的MS治疗方案不足以治疗不可逆的神经残疾。基于细胞的疗法在实验和临床应用方面取得了巨大进展,干细胞已被公认为是包括MS在内的许多神经退行性疾病再生治疗的潜在候选者。间充质干细胞(MSC)和诱导多能干细胞(iPSC)衍生的前体细胞可调节中枢神经系统(CNS)中的自身免疫反应,并促进动物模型中的内源性髓鞘再生和修复过程。本综述重点介绍了涉及间充质干细胞和iPSC衍生细胞在动物模型中的免疫调节和再生作用的研究,以及它们转化为MS免疫调节和神经再生治疗策略的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fafa/4463588/19bd19a1ee74/ijms-16-09283-g001.jpg

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