Neurosurgery, Emory University, 101 Woodruff Circle, Atlanta, GA 30322, USA.
Expert Opin Biol Ther. 2010 Mar;10(3):381-94. doi: 10.1517/14712590903514074.
Gene therapy is a promising strategy for the treatment of many neurological disorders that currently lack effective treatment. Recent improvements in vectorology and vector engineering have improved overall safety and delivery of viral vectors.
This review discusses the current state of viral vector development and clinical use, as well as routes of delivery, and clinical trials for neurological disorders.
Viral vectors may be delivered directly or remotely to the CNS, largely depending on the nature of the disease and the tropism of the vector. Nonetheless, delivery remains one of the major limitations of successful gene transfer to the CNS.
Although the majority of clinical trials have centered on gene replacement and neuroprotection approaches, the field is advancing in the direction of neuromodulation, gene silencing and other newer strategies.
基因治疗是一种很有前途的策略,用于治疗许多神经疾病,目前缺乏有效的治疗方法。最近在载体学和载体工程方面的改进提高了病毒载体的整体安全性和递送效率。
本综述讨论了病毒载体的开发和临床应用的现状,以及用于神经疾病的递送途径和临床试验。
病毒载体可以直接或远程递送到中枢神经系统,这在很大程度上取决于疾病的性质和载体的嗜性。尽管如此,递送到中枢神经系统的成功基因转移仍然是主要的限制因素之一。
虽然大多数临床试验都集中在基因替换和神经保护方法上,但该领域正在朝着神经调节、基因沉默和其他较新策略的方向发展。