Blömer U, Naldini L, Verma I M, Trono D, Gage F H
Salk Institute for Biological Studies, La Jolla, CA 92037-1099, USA.
Hum Mol Genet. 1996;5 Spec No:1397-404. doi: 10.1093/hmg/5.supplement_1.1397.
Gene therapy is a new method with potential for treating a broad range of acquired and inherited neurologic diseases, where the causative gene defect or deletion has been identified. In addition to gene replacement the application of gene products that reduce cellular dysfunction or death represent new therapeutic options. Gene transfer techniques to express novel proteins using different viral vectors in vitro and in vivo, as well as animal models and human trials will be reviewed in this article. We will focus on a new lentiviral vector as a recent gene transfer method and degenerative disorders of the CNS, and their related model systems.
基因治疗是一种有潜力治疗多种获得性和遗传性神经疾病的新方法,其中致病基因缺陷或缺失已被确定。除了基因替代,应用能减少细胞功能障碍或死亡的基因产物也代表了新的治疗选择。本文将综述在体外和体内使用不同病毒载体表达新蛋白质的基因转移技术,以及动物模型和人体试验。我们将重点关注一种新型慢病毒载体,作为一种最新的基因转移方法以及中枢神经系统的退行性疾病及其相关模型系统。