Deng Wu-Sheng, Ma Ke, Liang Bing, Liu Xiao-Yin, Xu Hui-You, Zhang Jian, Shi Heng-Yuan, Sun Hong-Tao, Chen Xu-Yi, Zhang Sai
College of Integrated Traditional Chinese and Western Medicine, Gansu University of Chinese Medicine, Lanzhou, Gansu Province, China.
Tianjin Key Laboratory of Neurotrauma Repair, Pingjin Hospital Brain Center, characteristic medical center of Chinese people's armed police force, Tianjin, China.
Neural Regen Res. 2020 Sep;15(9):1686-1700. doi: 10.4103/1673-5374.276340.
Currently, there is no effective strategy to promote functional recovery after a spinal cord injury. Collagen scaffolds can not only provide support and guidance for axonal regeneration, but can also serve as a bridge for nerve regeneration at the injury site. They can additionally be used as carriers to retain mesenchymal stem cells at the injury site to enhance their effectiveness. Hence, we hypothesized that transplanting human umbilical cord-mesenchymal stem cells on collagen scaffolds would enhance healing following acute complete spinal cord injury. Here, we test this hypothesis through animal studies and a phase I clinical trial. (1) Animal experiments: Models of completely transected spinal cord injury were established in rats and canines by microsurgery. Mesenchymal stem cells derived from neonatal umbilical cord tissue were adsorbed onto collagen scaffolds and surgically implanted at the injury site in rats and canines; the animals were observed after 1 week-6 months. The transplantation resulted in increased motor scores, enhanced amplitude and shortened latency of the motor evoked potential, and reduced injury area as measured by magnetic resonance imaging. (2) Phase I clinical trial: Forty patients with acute complete cervical injuries were enrolled at the Characteristic Medical Center of Chinese People's Armed Police Force and divided into two groups. The treatment group (n = 20) received collagen scaffolds loaded with mesenchymal stem cells derived from neonatal umbilical cord tissues; the control group (n = 20) did not receive the stem-cell loaded collagen implant. All patients were followed for 12 months. In the treatment group, the American Spinal Injury Association scores and activities of daily life scores were increased, bowel and urinary functions were recovered, and residual urine volume was reduced compared with the pre-treatment baseline. Furthermore, magnetic resonance imaging showed that new nerve fiber connections were formed, and diffusion tensor imaging showed that electrophysiological activity was recovered after the treatment. No serious complication was observed during follow-up. In contrast, the neurological functions of the patients in the control group were not improved over the follow-up period. The above data preliminarily demonstrate that the transplantation of human umbilical cord-mesenchymal stem cells on a collagen scaffold can promote the recovery of neurological function after acute spinal cord injury. In the future, these results need to be confirmed in a multicenter, randomized controlled clinical trial with a larger sample size. The clinical trial was approved by the Ethics Committee of the Characteristic Medical Center of Chinese People's Armed Police Force on February 3, 2016 (approval No. PJHEC-2016-A8). All animal experiments were approved by the Ethics Committee of the Characteristic Medical Center of Chinese People's Armed Police Force on May 20, 2015 (approval No. PJHEC-2015-D5).
目前,尚无促进脊髓损伤后功能恢复的有效策略。胶原蛋白支架不仅可为轴突再生提供支持和引导,还能在损伤部位充当神经再生的桥梁。此外,它们可用作载体,将间充质干细胞保留在损伤部位以增强其效果。因此,我们推测在胶原蛋白支架上移植人脐带间充质干细胞可促进急性完全性脊髓损伤后的愈合。在此,我们通过动物研究和I期临床试验来验证这一假设。(1)动物实验:通过显微手术在大鼠和犬类中建立完全横断性脊髓损伤模型。将源自新生儿脐带组织的间充质干细胞吸附到胶原蛋白支架上,并通过手术植入大鼠和犬类的损伤部位;术后对动物进行1周 - 6个月的观察。移植后运动评分增加,运动诱发电位的波幅增强、潜伏期缩短,磁共振成像测量显示损伤面积减小。(2)I期临床试验:中国人民武装警察部队特色医学中心招募了40例急性完全性颈椎损伤患者,并分为两组。治疗组(n = 20)接受负载有源自新生儿脐带组织的间充质干细胞的胶原蛋白支架;对照组(n = 20)未接受负载干细胞的胶原蛋白植入物。所有患者均随访12个月。与治疗前基线相比,治疗组的美国脊髓损伤协会评分和日常生活活动评分增加,肠道和泌尿功能恢复,残余尿量减少。此外,磁共振成像显示形成了新的神经纤维连接,扩散张量成像显示治疗后电生理活动恢复。随访期间未观察到严重并发症。相比之下,对照组患者的神经功能在随访期间未得到改善。上述数据初步证明,在胶原蛋白支架上移植人脐带间充质干细胞可促进急性脊髓损伤后神经功能的恢复。未来,这些结果需要在更大样本量的多中心、随机对照临床试验中得到证实。该临床试验于2016年2月3日获得中国人民武装警察部队特色医学中心伦理委员会批准(批准号:PJHEC - 2016 - A8)。所有动物实验于2015年5月20日获得中国人民武装警察部队特色医学中心伦理委员会批准(批准号:PJHEC - 2015 - D5)。