Safety and Feasibility of Autologous Mesenchymal Stem Cell Transplantation in Chronic Stroke in Indian patients. A four-year follow up.

IF 1.1 Q4 CELL & TISSUE ENGINEERING Journal of Stem Cells & Regenerative Medicine Pub Date : 2017-05-30 eCollection Date: 2017-01-01
Ashu Bhasin, Senthil S Kumaran, Rohit Bhatia, Sujata Mohanty, M V Padma Srivastava
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Abstract

Introduction: Stem cell (SC) therapy has been envisioned as a therapeutic vehicle to promote recovery in resistant neurological diseases. Knowing the logistics and paradigms in recovery processes after Stroke, clinicians have pioneered the transplantation therapy. This study presents four-year follow up of our previous trial transplanting bone-marrow-derived animal-free culture expanded intravenous mesenchymal stem cells (MSCs) in chronic stroke which was published in 2010. Methods: We performed an open-label, pilot trial on 12 patients with chronic stroke. Patients were allocated to two groups, those who received intravenous autologous ex vivo cultured mesenchymal stem cells (MSC group) or those who did not (control group), all followed for four years from the day of cell transplantation. Results: The reports have been optimistic regarding safety as we did not find any cell related side effects / mortality till 208th week. We observed that modified Barthel Index showed statistical significant improvement at 156 and 208 weeks of transplantation (95 % CI : -10.27 to 0.07; p =0.041) follow up in the MSC group as compared to controls. The 2nd and 3rd quartile for mBI in MSC group was 89 & 90 respectively suggesting good performance of patients in the stem cell group. The impairment scales i.e., Fugl Meyer, Ashworth tone scale, strength of hand muscles (MRC) did not show any significant improvement at 208th week which is similar to our previous published report. Conclusion: This follow up study primarily indicates safety, tolerance and applicability of autologous mesenchymal stem cells in Stroke. MSCs may act as "chaperones" or work through paracrine mechanisms leading to functional recovery post stroke.

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自体间充质干细胞移植治疗印度慢性脑卒中患者的安全性和可行性。四年的随访。
导读:干细胞(SC)治疗已被设想为一种治疗载体,以促进恢复的抵抗神经系统疾病。了解脑卒中后恢复过程的后勤和范例,临床医生开创了移植治疗。本研究对我们之前于2010年发表的移植骨髓来源的无动物培养扩大静脉注射间充质干细胞(MSCs)治疗慢性中风的试验进行了四年的随访。方法:我们对12例慢性脑卒中患者进行了一项开放标签的先导试验。患者被分为两组,静脉注射自体离体培养间充质干细胞组(MSC组)和未注射间充质干细胞组(对照组),从细胞移植之日起随访4年。结果:报告对安全性持乐观态度,因为直到第208周,我们没有发现任何细胞相关的副作用/死亡。我们观察到改良后的Barthel指数在移植156周和208周有统计学意义的改善(95% CI: -10.27 ~ 0.07;p =0.041),与对照组相比。干细胞组mBI的第二和第三四分位数分别为89和90,表明干细胞组患者表现良好。Fugl Meyer、Ashworth张力量表、手部肌肉力量(MRC)等损伤量表在第208周没有显示出任何显著的改善,这与我们之前发表的报告相似。结论:本随访研究初步提示自体间充质干细胞治疗脑卒中的安全性、耐受性和适用性。骨髓间充质干细胞可能作为“伴侣”或通过旁分泌机制导致中风后功能恢复。
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来源期刊
CiteScore
3.40
自引率
0.00%
发文量
5
审稿时长
14 weeks
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