向性
转导(生物物理学)
中枢神经系统
转基因
遗传增强
基因传递
脊髓
全身给药
神经科学
腺相关病毒
生物
病毒载体
组织向性
载体(分子生物学)
免疫学
医学
基因
病毒
遗传学
体内
生物化学
重组DNA
作者
Kimberly L. Pietersz,Raygene Martier,M. S. Baatje,Jolanda M.P. Liefhebber,Cynthia Brouwers,Stephan M. Pouw,L. Fokkert,Jacek Lubelski,Harald Petry,Gerard J.M. Martens,S J van Deventer,Pavlina Konstantinova,Bas Blits
出处
期刊:Gene Therapy
[Springer Nature]
日期:2020-08-15
卷期号:28 (7-8): 435-446
被引量:22
标识
DOI:10.1038/s41434-020-0178-0
摘要
Various administration routes of adeno-associated virus (AAV)-based gene therapy have been examined to target the central nervous system to answer the question what the most optimal delivery route is for treatment of the brain with certain indications. In this study, we evaluated AAV5 vector system for its capability to target the central nervous system via intrastriatal, intrathalamic or intracerebroventricular delivery routes in rats. AAV5 is an ideal candidate for gene therapy because of its relatively low level of existing neutralizing antibodies compared to other serotypes, and its broad tissue and cell tropism. Intrastriatal administration of AAV5-GFP resulted in centralized localized vector distribution and expression in the frontal part of the brain. Intrathalamic injection showed transduction and gradient expression from the rostral brain into lumbar spinal cord, while intracerebroventricular administration led to a more evenly, albeit relatively superficially distributed, transduction and expression throughout the central nervous system. To visualize the differences between localized and intra-cerebral spinal fluid administration routes, we compared intrastriatal to intracerebroventricular and intrathecal administration of AAV5-GFP. Together, our results demonstrate that for efficient transgene expression, various administration routes can be applied.
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