Yoshihisa Suzuki1, Namiko Ishikawa1, Kaoru Omae2, Tatsuya Hirai1, Katsunori Ohnishi3, Norihiko Nakano4, Hidetaka Nishida5, Toshio Nakatani6, Masanori Fukushima2, Chizuka Ide4. 1. Department of Plastic and Reconstructive Surgery, Kitano Hospital, Tazuke Kofukai Medical Research Institute, Osaka, Japan. 2. Translational Research Informatics Center, Kobe, Japan. 3. Ikesucho-clinic, Kyoto, Japan. 4. Institute of Regeneration and Rehabilitation, Faculty of Nursing and Rehabilitation, Aino University, Osaka, Japan. 5. Nakayama Veterinary Hospital, Nara, Japan. 6. Emergency and Critical Care Center, Kansai Medical University, Moriguchi, Osaka, Japan.
Abstract
PURPOSE: This study was conducted to assess the safety and feasibility of intrathecal transplantation of autologous bone marrow-derived mononuclear cells for the treatment of patients with spinal cord injury. METHODS: Ten patients were included in the study. Approximately 120 ml of bone marrow aspirate was obtained from bilateral iliac bone of patients with spinal cord injury. Isolation of mononuclear cells was performed using Ficoll density-gradient centrifugation. Bone marrow mononuclear cells were transplanted into cerebrospinal fluid by lumbar puncture. Functional tests were performed prior to the cell transplantation and six months after cell transplantation. The patients were carefully observed for up to six months. RESULTS: In 5 patients with AIS A prior to cell transplantation, 1 patient converted to AIS B six months after cell transplantation. In 5 patients with AIS B, 1 patient converted to AIS D and 2 patients to AIS C. MRI did not show any complication. Two patients showed slight anemia after aspiration of bone-marrow cells, which returned to normal level within a several weeks. CONCLUSION: The results of this study suggest that this method may be safe and feasible.
PURPOSE: This study was conducted to assess the safety and feasibility of intrathecal transplantation of autologous bone marrow-derived mononuclear cells for the treatment of patients with spinal cord injury. METHODS: Ten patients were included in the study. Approximately 120 ml of bone marrow aspirate was obtained from bilateral iliac bone of patients with spinal cord injury. Isolation of mononuclear cells was performed using Ficoll density-gradient centrifugation. Bone marrow mononuclear cells were transplanted into cerebrospinal fluid by lumbar puncture. Functional tests were performed prior to the cell transplantation and six months after cell transplantation. The patients were carefully observed for up to six months. RESULTS: In 5 patients with AIS A prior to cell transplantation, 1 patient converted to AIS B six months after cell transplantation. In 5 patients with AIS B, 1 patient converted to AIS D and 2 patients to AIS C. MRI did not show any complication. Two patients showed slight anemia after aspiration of bone-marrow cells, which returned to normal level within a several weeks. CONCLUSION: The results of this study suggest that this method may be safe and feasible.
Entities:
Keywords:
Central nervous system regeneration; bone marrow mononuclear cell; cell transplantation; clinical study; spinal cord injury treatment
Authors: M Hayashibe; T Homma; K Fujimoto; T Oi; N Yagi; M Kashihara; N Nishikawa; Y Ishizumi; S Abe; H Hashimoto; K Kanekiyo; H Imagita; C Ide; S Morioka Journal: Spinal Cord Date: 2015-10-20 Impact factor: 2.772