GSK249320, A Monoclonal Antibody Against the Axon Outgrowth Inhibition Molecule Myelin-Associated Glycoprotein, Improves Outcome of Rodents with Experimental Stroke

D. Cash, A. Easton, M. Mesquita, J. Beech, S. Williams, Andrew Lloyd, E. Irving, S. Cramer
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引用次数: 12

Abstract

Myelin-associated glycoprotein (MAG) is an inhibitor of axon growth. MAG levels increase after stroke. GSK249320 is a monoclonal antibody that neutralizes MAG-mediated inhibition and so may promote axon outgrowth and improve post-stroke outcomes. The current study tested the hypothesis that GSK249320 initiated 24 hours or 7 days after experimental stroke improves behavioural outcomes. Rats with right middle cerebral artery occlusion for 90 minutes were randomized to receive 6 weeks of intravenous (a) GSK249320 starting 24 hours post-stroke, (b) GSK249320 starting 7 days post-stroke, or (c) vehicle. Behavioral testing was performed over 7 weeks. Serial MRI demonstrated no differences in infarct volume across groups. Animals treated with GSK249320 24 hours post-stroke showed larger increases in Neuroscore (time X group, p = 0.0008) and staircase test (main effect of group, p = 0.0214) as compared to controls, but animals treated 7 days post-stroke showed no significant behavioral benefit. No significant results were found for the sticky tape or cylinder tests. A separate set of animals with experimental stroke received a single intravenous dose of GSK249320 or vehicle at 1 hour, 24 hours, 48 hours or 1 week post-stroke, and immunohistochemistry methods were used to measure GSK249320 distribution; GSK249320 was found in the ipsilesional hemisphere only, the extent of which increased with later times of injection. These data suggest that intravenous GSK249320 penetrates the lesion site and is associated with a small effect on functional outcomes when initiated 24 hours post-stroke and so support the translational potential of this monoclonal antibody as a restorative therapy for patients with stroke.
抗轴突生长抑制分子髓鞘相关糖蛋白的单克隆抗体GSK249320改善实验性脑卒中啮齿动物的预后
髓鞘相关糖蛋白(MAG)是轴突生长的抑制剂。中风后MAG水平升高。GSK249320是一种单克隆抗体,可中和mag介导的抑制,因此可促进轴突生长并改善卒中后预后。目前的研究验证了这样一种假设,即在实验性中风后24小时或7天开始使用GSK249320可以改善行为结果。右大脑中动脉闭塞90分钟的大鼠随机接受6周静脉注射(a)卒中后24小时开始,(b)卒中后7天开始,或(c)载药。行为测试进行了7周。系列MRI显示各组梗死体积无差异。GSK249320在脑卒中后24小时与对照组相比,神经评分(时间X组,p = 0.0008)和阶梯试验(主效应组,p = 0.0214)均有较大的提高,但在脑卒中后7天治疗的动物没有明显的行为改善。没有发现胶带或气缸测试的显著结果。另一组实验性脑卒中动物在脑卒中后1小时、24小时、48小时或1周接受单次静脉注射剂量的GSK249320或载药,并采用免疫组织化学方法测量GSK249320的分布;GSK249320仅存在于同侧半球,且随注射时间的延长而增加。这些数据表明,静脉注射GSK249320可穿透病变部位,并在卒中后24小时内对功能结果产生小影响,因此支持该单克隆抗体作为卒中患者恢复性治疗的转化潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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