造血和间充质干细胞移植作为多发性硬化症的有效治疗方法的发展。

IF 1.5 Q4 CELL BIOLOGY
American journal of stem cells Pub Date : 2013-06-30 Print Date: 2013-01-01
Jameson P Holloman, Calvin C Ho, Arushi Hukki, Jennifer L Huntley, G Ian Gallicano
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引用次数: 0

摘要

本文探讨了干细胞治疗多发性硬化症(MS)的现状和未来意义。多发性硬化症是年轻人中最常见的神经系统疾病,全世界约有200万人受到影响。目前还没有治愈多发性硬化症的方法,多发性硬化症的标准治疗包括疾病改善药物,这些药物可以减轻多发性硬化症的症状,但这些药物具有不良副作用,并且在许多多发性硬化症患者中对预防疾病进展无效。造血干细胞移植(HSCT)于1995年首次用于治疗严重快速进展的多发性硬化症患者,HSCT治疗方案已演变为一种强度较低的调节方案,目前在治疗不同疾病严重程度的患者中显示出疗效,在早期伴有活动性中枢神经系统炎症的快速进展多发性硬化症患者中效果最佳。间充质干细胞疗法(Mesenchymal stem cell therapy, MSCT)是一种实验性干细胞疗法,目前正处于临床试验阶段。动物模型和早期临床试验表明,MSCT可能是一种促进多发性硬化症患者神经再生和免疫调节的低风险治疗方法。具体来说,神经祖细胞和胎盘来源的间充质干细胞为MS的实际治疗提供了最好的希望。干细胞治疗,也许是一种组合治疗方法,为MS的更好治疗提供了希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The development of hematopoietic and mesenchymal stem cell transplantation as an effective treatment for multiple sclerosis.

This article examines the current use and future implications of stem cell therapy in treating Multiple Sclerosis (MS). MS is the most common neurological disease in young adults, affecting approximately two million people worldwide. Currently there is no cure for MS. The standard treatment of MS involves disease-modifying drugs, which work to alleviate the symptoms of MS. However, these drugs carry adverse side effects and are ineffective in preventing disease progression in many MS patients. Hematopoietic stem cell transplantation (HSCT) was first used in 1995 to treat patients with severe rapidly progressing MS. The HSCT treatment protocol has evolved into a less intense conditioning regimen that is currently demonstrating efficacy in treating patients with variable disease severity-with best results in early-stage rapidly progressing MS patients with active CNS inflammation. Mesenchymal stem cell therapy (MSCT) is an experimental stem cell therapy currently undergoing clinical trials. Animal models and early clinical trials have shown promise that MSCT might be a low risk treatment to precipitate neuroregeneration and immunomodulation in MS patients. Specifically, neuroprogenitor and placental-derived mesenchymal stem cells offer the best hope for a practical treatment for MS. Stem cell therapy, and perhaps a combinatorial therapeutic approach, holds promise for a better treatment for MS.

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