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A First-in-Human, Phase I Study of Neural Stem Cell Transplantation for Chronic Spinal Cord Injury

机译:第一期,I阶段研究神经干细胞移植治疗慢性脊髓损伤

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We tested the feasibility and safety of human-spinal-cord-derived neural stem cell (NSI-566) transplantation for the treatment of chronic spinal cord injury (SCI). In this clinical trial, four subjects with T2–T12 SCI received treatment consisting of removal of spinal instrumentation, laminectomy, and durotomy, followed by six midline bilateral stereotactic injections of NSI-566 cells. All subjects tolerated the procedure well and there have been no serious adverse events to date (18–27?months post-grafting). In two subjects, one to two levels of neurological improvement were detected using ISNCSCI motor and sensory scores. Our results support the safety of NSI-566 transplantation into the SCI site and early?signs of potential efficacy in three of the subjects warrant further exploration of NSI-566 cells in dose escalation studies. Despite these encouraging secondary data, we emphasize that this safety trial lacks statistical power or a control group needed to evaluate functional changes resulting from cell grafting.
机译:我们测试了人脊髓源性神经干细胞(NSI-566)移植治疗慢性脊髓损伤(SCI)的可行性和安全性。在该临床试验中,具有T2-T12 SCI的四次受试者接受了由去除脊柱仪器,椎骨切除术和杜孔的治疗,其次是NSI-566细胞的六个中线双侧立体术注射。所有受试者均宽容,迄今为止没有严重的不良事件(嫁接后18-27个月)。在两个受试者中,使用ISNCSCI电动机和感官分数检测到一到两种水平的神经改善。我们的结果支持NSI-566移植到SCI网站的安全性,并提前存在?三个受试者的潜在疗效的迹象是在剂量升级研究中进一步探索NSI-566细胞。尽管有这些令人鼓舞的二级数据,我们强调,这种安全试验缺乏统计功率或对照组所需的控制组,以评估由细胞嫁接产生的功能变化。

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