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AAV ablates neurogenesis in the adult murine hippocampus.AAV 可消融成年鼠海马体中的神经发生。
Elife. 2021 Jul 14;10:e59291. doi: 10.7554/eLife.59291.
3
Comparative Effectiveness of Intracerebroventricular, Intrathecal, and Intranasal Routes of AAV9 Vector Administration for Genetic Therapy of Neurologic Disease in Murine Mucopolysaccharidosis Type I.AAV9载体经脑室内、鞘内和鼻内给药途径对小鼠I型粘多糖贮积症神经疾病进行基因治疗的比较有效性
Front Mol Neurosci. 2021 May 10;14:618360. doi: 10.3389/fnmol.2021.618360. eCollection 2021.
4
Systemic AAV6-synapsin-GFP administration results in lower liver biodistribution, compared to AAV1&2 and AAV9, with neuronal expression following ultrasound-mediated brain delivery.全身性 AAV6-synapsin-GFP 给药与 AAV1&2 和 AAV9 相比,肝脏生物分布较低,经超声介导的脑内给药后具有神经元表达。
Sci Rep. 2021 Jan 21;11(1):1934. doi: 10.1038/s41598-021-81046-5.
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Pelizaeus-Merzbacher Disease: Molecular and Cellular Pathologies and Associated Phenotypes.佩利兹-梅茨巴赫病:分子和细胞病理学及相关表型。
Adv Exp Med Biol. 2019;1190:201-216. doi: 10.1007/978-981-32-9636-7_13.
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Gene suppressing therapy for Pelizaeus-Merzbacher disease using artificial microRNA.利用人工 microRNA 进行 Pelizaeus-Merzbacher 病的基因抑制治疗。
JCI Insight. 2019 May 16;4(10). doi: 10.1172/jci.insight.125052.
7
Ultrasound-responsive nanobubble-mediated gene transfection in the cerebroventricular region by intracerebroventricular administration in mice.通过脑室内给药,在小鼠脑室区域实现超声响应纳米泡介导的基因转染。
Eur J Pharm Biopharm. 2019 Apr;137:1-8. doi: 10.1016/j.ejpb.2019.02.003. Epub 2019 Feb 7.
8
Developmental disabilities among children younger than 5 years in 195 countries and territories, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016.1990-2016 年全球 195 个国家和地区 5 岁以下儿童发育障碍发生率:2016 年全球疾病负担研究的系统分析。
Lancet Glob Health. 2018 Oct;6(10):e1100-e1121. doi: 10.1016/S2214-109X(18)30309-7. Epub 2018 Aug 29.
9
Efficient CNS targeting in adult mice by intrathecal infusion of single-stranded AAV9-GFP for gene therapy of neurological disorders.通过鞘内注射单链AAV9-GFP实现成年小鼠中枢神经系统的高效靶向,用于神经疾病的基因治疗。
Gene Ther. 2017 May;24(5):325-332. doi: 10.1038/gt.2017.18. Epub 2017 Apr 20.
10
Ultrasound-mediated drug delivery to the brain: principles, progress and prospects.超声介导的脑部药物递送:原理、进展与展望
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聚焦超声作为腺相关病毒基因治疗的助力工具:通过脑室内给药用于幼年小鼠

Focused Ultrasounds as an Adeno-Associated Virus Gene Therapy-Empowering Tool in Juvenile Mice via Intracerebroventricular Administration.

作者信息

Zappala Alessandro, Li Heng, Inoue Ken

机构信息

Department Mental Retardation & Birth Defect Research, National Center of Neurology & Psychiatry, National Institute of Neuroscience, Tokyo, Japan.

出版信息

Hum Gene Ther. 2024 Dec;35(23-24):989-999. doi: 10.1089/hum.2024.108. Epub 2024 Nov 25.

DOI:10.1089/hum.2024.108
PMID:39585211
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11659451/
Abstract

Systemic delivery of adeno-associated virus (AAV) vectors targeting the central nervous system has the potential to solve many neurodevelopmental disorders, yet it is made difficult by the filtering effect of the blood-brain barrier and systemic complications. To overcome this limitation, we attempted to inject a Venus-expressing, oligodendrocyte-selective AAV9 viral vector in the ventricles together with lipid microbubbles and subjected them to focused ultrasound (FUS); the resulting mechanical stimulation on the brain ventricles is able to open small, temporary gaps from which vector particles can leak and spread. Our findings indicate that FUS can increase viral vector diffusion across both the anteroposterior and left-right axes without influencing cell tropism; significant effects were found with 60 and 90 s exposure time, but no effects were observed with longer intervals. Taken together, these results highlight a new strategy for the safe and effective delivery of viral vectors and offer new perspectives for the development and application of gene therapies for central nervous system diseases.

摘要

系统性递送靶向中枢神经系统的腺相关病毒(AAV)载体有潜力解决许多神经发育障碍问题,但血脑屏障的过滤作用和全身并发症使其面临困难。为克服这一限制,我们尝试将表达金星蛋白的少突胶质细胞选择性AAV9病毒载体与脂质微泡一起注入脑室,并对其施加聚焦超声(FUS);由此产生的对脑室的机械刺激能够打开小的临时间隙,载体颗粒可从中泄漏和扩散。我们的研究结果表明,FUS可增加病毒载体在前后轴和左右轴上的扩散,而不影响细胞嗜性;在60秒和90秒的暴露时间下发现了显著效果,但更长时间间隔未观察到效果。综上所述,这些结果突出了一种安全有效递送病毒载体的新策略,并为中枢神经系统疾病基因治疗的开发和应用提供了新的视角。