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慢性缺血性卒中的自体静脉内单核干细胞治疗

Autologous intravenous mononuclear stem cell therapy in chronic ischemic stroke.

作者信息

Bhasin A, Srivastava Mv, Bhatia R, Mohanty S, Kumaran Ss, Bose S

机构信息

All India Institute of Medical Sciences , New Delhi, India, 110029.

University of Texas , USA.

出版信息

J Stem Cells Regen Med. 2012 Nov 26;8(3):181-9. doi: 10.46582/jsrm.0803011. eCollection 2012.

Abstract

BACKGROUND

The regenerative potential of brain has led to emerging therapies that can cure clinico-motor deficits after neurological diseases. Bone marrow mononuclear cell therapy is a great hope to mankind as these cells are feasible, multipotent and aid in neurofunctional gains in Stroke patients.

AIMS

This study evaluates safety, feasibility and efficacy of autologous mononuclear (MNC) stem cell transplantation in patients with chronic ischemic stroke (CIS) using clinical scores and functional imaging (fMRI and DTI).

DESIGN

Non randomised controlled observational study Study: Twenty four (n=24) CIS patients were recruited with the inclusion criteria as: 3 months-2years of stroke onset, hand muscle power (MRC grade) at least 2; Brunnstrom stage of recovery: II-IV; NIHSS of 4-15, comprehendible. Fugl Meyer, modified Barthel Index (mBI) and functional imaging parameters were used for assessment at baseline, 8 weeks and at 24 weeks. Twelve patients were administered with mean 54.6 million cells intravenously followed by 8 weeks of physiotherapy. Twelve patients served as controls. All patients were followed up at 24 weeks.

OUTCOMES

The laboratory and radiological outcome measures were within normal limits in MNC group. Only mBI showed statistically significant improvement at 24 weeks (p<0.05) whereas the mean FM, MRC, Ashworth tone scores in the MNC group were high as compared to control group. There was an increased number of cluster activation of Brodmann areas BA 4, BA 6 post stem cell infusion compared to controls indicating neural plasticity. Cell therapy is safe and feasible which may facilitate restoration of function in CIS.

摘要

背景

大脑的再生潜力催生了一些新兴疗法,这些疗法能够治愈神经系统疾病后的临床运动功能障碍。骨髓单个核细胞疗法给人类带来了巨大希望,因为这些细胞具有可行性、多能性,并且有助于中风患者获得神经功能改善。

目的

本研究使用临床评分和功能成像(功能磁共振成像和弥散张量成像)评估自体单个核(MNC)干细胞移植治疗慢性缺血性中风(CIS)患者的安全性、可行性和疗效。

设计

非随机对照观察性研究

研究

招募了24例CIS患者,纳入标准为:中风发作3个月至2年,手部肌肉力量(医学研究委员会肌力分级)至少为2级;Brunnstrom恢复阶段:II-IV级;美国国立卫生研究院卒中量表(NIHSS)评分为4-15分且可理解。在基线、8周和24周时使用Fugl Meyer量表、改良巴氏指数(mBI)和功能成像参数进行评估。12例患者静脉注射平均5460万个细胞,随后进行8周的物理治疗。12例患者作为对照组。所有患者均随访24周。

结果

MNC组的实验室和影像学结果指标均在正常范围内。仅mBI在24周时显示出统计学上的显著改善(p<0.05),而MNC组的平均FM、MRC、Ashworth肌张力评分与对照组相比更高。与对照组相比,干细胞输注后Brodmann区域BA 4、BA 6的簇状激活数量增加,表明神经可塑性。细胞疗法是安全可行的,可能有助于CIS患者功能的恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d0/3908296/531c45e5c38b/jsrm-08-185-g010.jpg

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