Chandran Jayanth, Chowdhury Ekram Ahmed, Perkinton Michael, Jamier Tanguy, Sutton Daniel, Wu Shengjia, Dobson Claire, Shah Dhaval K, Chessell Iain, Meno-Tetang Guy M L
Discovery Sciences, Biopharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Department of Pharmaceutical Sciences, The State University of New York at Buffalo, Buffalo, NY, USA.
Gene Ther. 2023 Feb;30(1-2):132-141. doi: 10.1038/s41434-022-00346-1. Epub 2022 May 30.
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.
在全身递送腺相关病毒(AAV)后,要实现对脑和脊髓的高效转导存在挑战,这促使在临床试验中采用将病毒直接注入中枢神经系统(CNS)的替代给药途径。然而,比较不同的直接脑内AAV注射的数据仍然有限,这使得难以选择最佳途径。在此,我们在成年大鼠中通过纹状体内(IST)、小脑延髓池(ICM)和腰段鞘内(LIT)途径测试了AAV9-增强绿色荧光蛋白(egfp)和AAV9-荧光素酶(fLuc)的递送,并评估了载体在脑、脊髓和外周组织中的分布及转导情况。我们发现,与ICM或LIT相比,IST输注可导致纹状体、丘脑和皮质中强大的转基因表达,外周组织转导及抗AAV9衣壳滴度较低。与其他途径相比,ICM递送在更多脑区提供了强烈的绿色荧光蛋白(GFP)和荧光素酶表达,并且在脊髓中的表达与LIT注射相似,而LIT本身在很大程度上未能转导大鼠脑。我们的数据突出了每种直接CNS递送途径的优缺点,这将有助于未来的临床靶向治疗。