Kimura Seigo, Harashima Hideyoshi
Laboratory for Molecular Design of Pharmaceutics, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
Laboratory of Innovative Nanomedicine, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
Pharmaceutics. 2020 Dec 15;12(12):1216. doi: 10.3390/pharmaceutics12121216.
The era of the aging society has arrived, and this is accompanied by an increase in the absolute numbers of patients with neurological disorders, such as Alzheimer's disease (AD) and Parkinson's disease (PD). Such neurological disorders are serious costly diseases that have a significant impact on society, both globally and socially. Gene therapy has great promise for the treatment of neurological disorders, but only a few gene therapy drugs are currently available. Delivery to the brain is the biggest hurdle in developing new drugs for the central nervous system (CNS) diseases and this is especially true in the case of gene delivery. Nanotechnologies such as viral and non-viral vectors allow efficient brain-targeted gene delivery systems to be created. The purpose of this review is to provide a comprehensive review of the current status of the development of successful drug delivery to the CNS for the treatment of CNS-related disorders especially by gene therapy. We mainly address three aspects of this situation: (1) blood-brain barrier (BBB) functions; (2) adeno-associated viral (AAV) vectors, currently the most advanced gene delivery vector; (3) non-viral brain targeting by non-invasive methods.
老龄化社会的时代已经到来,随之而来的是神经疾病患者的绝对数量增加,如阿尔茨海默病(AD)和帕金森病(PD)。此类神经疾病是严重的高成本疾病,在全球范围内对社会都有重大影响。基因治疗在神经疾病治疗方面前景广阔,但目前只有少数基因治疗药物可用。向大脑给药是开发中枢神经系统(CNS)疾病新药的最大障碍,在基因递送方面尤其如此。病毒和非病毒载体等纳米技术能够创建高效的脑靶向基因递送系统。本综述的目的是全面回顾目前成功向中枢神经系统给药以治疗中枢神经系统相关疾病,特别是通过基因治疗的发展现状。我们主要探讨这种情况的三个方面:(1)血脑屏障(BBB)功能;(2)腺相关病毒(AAV)载体,目前最先进的基因递送载体;(3)通过非侵入性方法实现非病毒脑靶向。