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自体间充质干细胞移植治疗印度慢性中风患者的安全性和可行性。四年随访。

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

作者信息

Bhasin Ashu, Kumaran Senthil S, Bhatia Rohit, Mohanty Sujata, Srivastava M V Padma

机构信息

Department of Neurology.

出版信息

J Stem Cells Regen Med. 2017 May 30;13(1):14-19. doi: 10.46582/jsrm.1301003. eCollection 2017.

Abstract

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. We performed an open-label, pilot trial on 12 patients with chronic stroke. Patients were allocated to two groups, those who received intravenous autologous cultured mesenchymal stem cells (MSC group) or those who did not (control group), all followed for four years from the day of cell transplantation. 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. 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.

摘要

干细胞(SC)疗法一直被视为一种促进难治性神经系统疾病康复的治疗手段。鉴于了解中风后恢复过程中的相关情况和模式,临床医生率先开展了移植治疗。本研究展示了我们之前于2010年发表的一项试验的四年随访结果,该试验将无动物培养扩增的骨髓来源静脉间充质干细胞(MSCs)移植到慢性中风患者体内。我们对12例慢性中风患者进行了一项开放标签的试点试验。患者被分为两组,一组接受静脉自体培养的间充质干细胞(MSC组),另一组不接受(对照组),从细胞移植当天起均随访四年。关于安全性的报告较为乐观,因为直到第208周我们都未发现任何与细胞相关的副作用/死亡率。我们观察到,与对照组相比,MSC组在移植后第156周和第208周时改良巴氏指数显示出统计学上的显著改善(95%置信区间:-10.27至0.07;p = 0.041)。MSC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。在第208周时,功能障碍量表,即Fugl Meyer量表、Ashworth肌张力量表、手部肌肉力量(MRC)量表均未显示出任何显著改善,这与我们之前发表的报告相似。这项随访研究主要表明自体间充质干细胞在中风治疗中的安全性、耐受性和适用性。间充质干细胞可能充当“伴侣分子”或通过旁分泌机制发挥作用,从而导致中风后功能恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/968b/5494434/5ba37e856f18/jsrm-13-14-g001.jpg

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