Phillips R G, Monje M L, Giuli L C, Meier T J, Yenari M A, Kunis D, Sapolsky R M
Department of Biological Sciences, Stanford University, Stanford, CA 94305-5020 USA.
Gene Ther. 2001 Apr;8(8):579-85. doi: 10.1038/sj.gt.3301397.
If neuronal gene therapy is to be clinically useful, it is necessary to demonstrate neuroprotection when the gene is introduced after insult. We now report equivalent neuronal protection if calbindin D(28K) gene transfer via herpes simplex virus amplicon vector occurs immediately, 30 min, or 1 h after an excitotoxic insult, but not after a 4 h delay. Behavioral performance was evaluated for immediate and 1 h delay groups using a hippocampal-dependent task. Despite equivalent magnitude and pattern of sparing of neurons with the immediate and 1 h delay approaches, the delay animals took a significantly longer time after insult to return to normal performance.
如果神经元基因疗法要在临床上发挥作用,那么在损伤后导入基因时必须证明其具有神经保护作用。我们现在报告,如果通过单纯疱疹病毒扩增载体进行钙结合蛋白D(28K)基因转移在兴奋性毒性损伤后立即、30分钟或1小时进行,而不是在延迟4小时后进行,则会产生同等的神经元保护作用。使用依赖海马体的任务对立即和延迟1小时组的行为表现进行了评估。尽管立即和延迟1小时方法在神经元保留的程度和模式上相同,但延迟组动物在损伤后恢复到正常表现所需的时间明显更长。