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抗高迁移率族蛋白B1抗体在脊髓损伤小鼠模型中的治疗时间窗

Therapeutic time window of anti-high mobility group box-1 antibody administration in mouse model of spinal cord injury.

作者信息

Nakajo Masahide, Uezono Naohiro, Nakashima Hideyuki, Wake Hidenori, Komiya Setsuro, Nishibori Masahiro, Nakashima Kinichi

机构信息

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.

出版信息

Neurosci Res. 2019 Apr;141:63-70. doi: 10.1016/j.neures.2018.03.004. Epub 2018 Mar 28.

Abstract

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.

摘要

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。

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