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间充质干细胞移植作为多发性硬化症治疗方法的治疗潜力:国际 MSCT 研究组共识报告。

The therapeutic potential of mesenchymal stem cell transplantation as a treatment for multiple sclerosis: consensus report of the International MSCT Study Group.

机构信息

University of Ottawa, Ottawa Hospital Research Institute, Ontario, Canada.

出版信息

Mult Scler. 2010 Apr;16(4):503-10. doi: 10.1177/1352458509359727. Epub 2010 Jan 19.

Abstract

Current therapies for multiple sclerosis effectively reduce inflammation, but do little in terms of repair to the damaged central nervous system. Cell-based therapies may provide a new strategy for bolstering regeneration and repair through neuro-axonal protection or remyelination. Mesenchymal stem cells modulate pathological responses in experimental autoimmune encephalitis, alleviating disease, but also stimulate repair of the central nervous system through the release of soluble factors. Autologous and allogeneic mesenchymal stem cells have been safely administered to individuals with hemato-oncological diseases and in a limited number of patients with multiple sclerosis. It is therefore reasonable to move mesenchymal stem cells transplantation into properly controlled human studies to explore their potential as a treatment for multiple sclerosis. Since it is likely that the first such studies will probably involve only small numbers of patients in a few centers, we formed an international panel comprising multiple sclerosis neurology and stem cell experts, as well as immunologists. The aims were to derive a consensus on the utilization of mesenchymal stem cells for the treatment of multiple sclerosis, along with protocols for the culture of the cells and the treatment of patients. This article reviews the consensus derived from our group on the rationale for mesenchymal stem cell transplantation, the methodology for generating mesenchymal stem cells and the first treatment protocol for multiple sclerosis patients.

摘要

目前多发性硬化症的治疗方法可以有效减轻炎症,但对于受损的中枢神经系统几乎没有修复作用。基于细胞的疗法可能通过神经-轴突保护或髓鞘再生提供一种新的增强再生和修复的策略。间充质干细胞可调节实验性自身免疫性脑脊髓炎中的病理反应,从而缓解疾病,但也可通过释放可溶性因子刺激中枢神经系统的修复。自体和同种异体间充质干细胞已安全地用于血液系统恶性肿瘤患者和少数多发性硬化症患者。因此,将间充质干细胞移植到适当控制的人体研究中以探索其作为多发性硬化症治疗方法的潜力是合理的。由于第一个此类研究可能仅涉及少数几个中心的少数患者,因此我们组成了一个由多发性硬化症神经病学和干细胞专家以及免疫学家组成的国际小组。目的是就间充质干细胞治疗多发性硬化症的应用达成共识,以及细胞培养和患者治疗的方案。本文综述了我们小组关于间充质干细胞移植的基本原理、间充质干细胞的生成方法以及多发性硬化症患者的第一个治疗方案的共识。

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