转导(生物物理学)
脊髓
腰脊髓
生物
神经科学
丘脑
中枢神经系统
基因传递
腰椎
纹状体
转基因
全身给药
遗传增强
医学
药理学
解剖
体内
生物技术
生物化学
基因
多巴胺
作者
Jayanth Chandran,Ekram Ahmed Chowdhury,Michael S. Perkinton,Tanguy Jamier,Daniel Sutton,Shengjia Wu,Claire Dobson,Dhaval K. Shah,Iain P. Chessell,Guy Meno‐Tetang
出处
期刊:Gene Therapy
[Springer Nature]
日期:2022-05-30
卷期号:30 (1-2): 132-141
被引量:7
标识
DOI:10.1038/s41434-022-00346-1
摘要
Challenges in obtaining efficient transduction of brain and spinal cord following systemic AAV delivery have led to alternative administration routes being used in clinical trials that directly infuse the virus into the CNS. However, data comparing different direct AAV injections into the brain remain limited making it difficult to choose optimal routes. Here we tested both AAV9-egfp and AAV9-fLuc delivery via intrastriatal (IST), intracisterna magna (ICM) and lumbar intrathecal (LIT) routes in adult rats and assessed vector distribution and transduction in brain, spinal cord and peripheral tissues. We find that IST infusion leads to robust transgene expression in the striatum, thalamus and cortex with lower peripheral tissue transduction and anti-AAV9 capsid titers compared to ICM or LIT. ICM delivery provided strong GFP and luciferase expression across more brain regions than the other routes and similar expression in the spinal cord to LIT injections, which itself largely failed to transduce the rat brain. Our data highlight the strengths and weaknesses of each direct CNS delivery route which will help with future clinical targeting.
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