The potential of human umbilical cord-derived mesenchymal stem cells as a novel cellular therapy for multiple sclerosis.

IF 3.2 4区 医学 Q3 CELL & TISSUE ENGINEERING Cell Transplantation Pub Date : 2014-01-01 Epub Date: 2014-11-05 DOI:10.3727/096368914X685005
Jin-Feng Li, Da-Jin Zhang, Tongchao Geng, Lin Chen, Hongyun Huang, Hong-Lei Yin, Yu-zhen Zhang, Ji-Yu Lou, Bingzhen Cao, Yun-Liang Wang
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引用次数: 88

Abstract

Multiple sclerosis (MS) is a complex disease of neurological disability, affecting more than 300 out of every 1 million people in the world. The purpose of the study was to evaluate the therapeutic effects of human umbilical cord-derived mesenchymal stem cell (hUC-MSC) transplantation in MS patients. Twenty-three patients were enrolled in this study, and 13 of them were given hUC-MSC therapy at the same time as anti-inflammatory treatment, whereas the control patients received the anti-inflammatory treatment only. Treatment schedule included 1,000 mg/kg of methylprednisolone intravenously (IV) daily for 3 days and then 500 mg/kg for 2 days, followed by oral prednisone 1 mg/kg/day for 10 days. The dosage of prednisone was then reduced by 5 mg every 2 weeks until reaching a 5-mg/day maintenance dosage. Intravenous infusion of hUC-MSCs was applied three times in a 6-week period for each patient. The overall symptoms of the hUC-MSC-treated patients improved compared to patients in the control group. Both the EDSS scores and relapse occurrence were significantly lower than those of the control patients. Inflammatory cytokines were assessed, and the data demonstrated a shift from Th1 to Th2 immunity in hUC-MSC-treated patients. Our data demonstrated a high potential for hUC-MSC treatment of MS. This manuscript is published as part of the International Association of Neurorestoratology (IANR) special issue of Cell Transplantation.

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人脐带源性间充质干细胞作为多发性硬化症新细胞疗法的潜力。
多发性硬化症(MS)是一种复杂的神经功能障碍疾病,世界上每100万人中就有300多人受到影响。本研究的目的是评估人脐带源性间充质干细胞(hUC-MSC)移植对多发性硬化症患者的治疗效果。本研究共纳入23例患者,其中13例患者在抗炎治疗的同时给予hUC-MSC治疗,对照组患者仅给予抗炎治疗。治疗方案包括每日1000mg /kg甲基强的松静脉注射(IV) 3天,然后500mg /kg连续2天,随后口服强的松1mg /kg/天,连续10天。然后每2周减少5mg泼尼松的剂量,直到达到5mg /天的维持剂量。每位患者在6周内静脉输注hUC-MSCs 3次。与对照组患者相比,huc - msc治疗患者的总体症状得到改善。EDSS评分和复发率均显著低于对照组。对炎症细胞因子进行了评估,数据显示huc - msc治疗的患者从Th1免疫转变为Th2免疫。我们的数据表明hUC-MSC治疗多发性硬化症具有很高的潜力。这篇论文发表在国际神经修复学会(IANR)《细胞移植》特刊上。
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来源期刊
Cell Transplantation
Cell Transplantation 生物-细胞与组织工程
CiteScore
6.00
自引率
3.00%
发文量
97
审稿时长
6 months
期刊介绍: Cell Transplantation, The Regenerative Medicine Journal is an open access, peer reviewed journal that is published 12 times annually. Cell Transplantation is a multi-disciplinary forum for publication of articles on cell transplantation and its applications to human diseases. Articles focus on a myriad of topics including the physiological, medical, pre-clinical, tissue engineering, stem cell, and device-oriented aspects of the nervous, endocrine, cardiovascular, and endothelial systems, as well as genetically engineered cells. Cell Transplantation also reports on relevant technological advances, clinical studies, and regulatory considerations related to the implantation of cells into the body in order to provide complete coverage of the field.
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