Nakajo Masahide, Uezono Naohiro, Nakashima Hideyuki, Wake Hidenori, Komiya Setsuro, Nishibori Masahiro, Nakashima Kinichi
Department of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8581, Japan; Department of Orthopaedic Surgery, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima 890-8520, Japan.
Department of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8581, Japan.
Neurosci Res. 2019 Apr;141:63-70. doi: 10.1016/j.neures.2018.03.004. Epub 2018 Mar 28.
Spinal cord injury (SCI) is a devastating neurologic disorder that often leads to permanent disability, and there is no effective treatment for it. High mobility group box-1 (HMGB1) is a damage-associated molecular protein that triggers sterile inflammation upon injuries. We have previously shown that two administrations of neutralizing monoclonal antibody (mAb) against HMGB1 (immediately after (0 h) and 6 h after) SCI dramatically improves functional recovery after SCI in mice. However, when considering clinical application, 0 h after SCI is not practical. Therefore, in this study, we examined the therapeutic time window of the mAb administration. Injection at 3 h after SCI significantly improved the functional recovery comparably to injection immediately after SCI, while injection at 6 h was less effective, and injection at 9 or 12 h had no therapeutic effect. We also found beneficial effects of injection at 3 h after injury on blood-spinal cord barrier maintenance, inflammatory-related gene expression and preservation of the damaged spinal cord tissue. Taken together, our results suggest that a single administration of anti-HMGB1 mAb within a proper time window could be a novel and potential therapeutic strategy for SCI.
脊髓损伤(SCI)是一种毁灭性的神经系统疾病,常常导致永久性残疾,且尚无有效的治疗方法。高迁移率族蛋白B1(HMGB1)是一种损伤相关分子蛋白,在损伤时引发无菌性炎症。我们之前已经表明,在脊髓损伤后立即(0小时)和6小时给予两种针对HMGB1的中和单克隆抗体(mAb),可显著改善小鼠脊髓损伤后的功能恢复。然而,考虑到临床应用,脊髓损伤后0小时并不实际。因此,在本研究中,我们研究了单克隆抗体给药的治疗时间窗。脊髓损伤后3小时注射与脊髓损伤后立即注射相比,显著改善了功能恢复,而6小时注射效果较差,9或12小时注射则没有治疗效果。我们还发现损伤后3小时注射对血脊髓屏障维持、炎症相关基因表达以及受损脊髓组织的保存具有有益作用。综上所述,我们的结果表明,在适当的时间窗内单次给予抗HMGB1单克隆抗体可能是一种针对脊髓损伤的新型潜在治疗策略。