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磁共振成像引导的聚焦超声用于将重组腺相关病毒靶向递送至大脑。

MRI-Guided Focused Ultrasound for Targeted Delivery of rAAV to the Brain.

作者信息

Noroozian Zeinab, Xhima Kristiana, Huang Yuexi, Kaspar Brian K, Kügler Sebastian, Hynynen Kullervo, Aubert Isabelle

机构信息

Brain Sciences, Biological Sciences, Sunnybrook Research Institute, Toronto, ON, Canada.

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.

出版信息

Methods Mol Biol. 2019;1950:177-197. doi: 10.1007/978-1-4939-9139-6_10.

Abstract

Recombinant adeno-associated viral (rAAV) vectors are a promising tool for therapeutic gene delivery to the brain. However, the delivery of rAAVs across the blood-brain barrier (BBB) and entry into the brain remains a major challenge for rAAV-based gene therapy. To circumvent this limitation, transcranial MRI-guided focused ultrasound (MRIgFUS) combined with intravenously injected microbubbles has been used to transiently and reversibly increase BBB permeability in targeted brain regions. Systemic administration of rAAVs at the time of sonication with focused ultrasound (FUS) facilitates the passage of rAAVs through the BBB and into the brain parenchyma. We and others have demonstrated that FUS-mediated rAAV delivery to the brain results in efficient transduction and transgene expression in vivo. Using this approach, the dose of intravenously injected rAAV variants that can cross the BBB can be reduced by 100 times, achieving significant transgene expression in the brain parenchyma with reduced peripheral transduction. Moreover, this strategy can be used to deliver rAAV variants that do not cross the BBB from the blood to selected brain regions. Here, we provide a detailed protocol for FUS-induced BBB permeability for targeted rAAV delivery to the brain of adult mice and rats.

摘要

重组腺相关病毒(rAAV)载体是一种将治疗性基因递送至大脑的有前景的工具。然而,rAAV穿越血脑屏障(BBB)并进入大脑仍然是基于rAAV的基因治疗的一项重大挑战。为了克服这一限制,经颅MRI引导的聚焦超声(MRIgFUS)联合静脉注射微泡已被用于短暂且可逆地增加靶向脑区的BBB通透性。在聚焦超声(FUS)超声处理时全身给予rAAV有助于rAAV穿过BBB并进入脑实质。我们和其他人已经证明,FUS介导的rAAV递送至大脑可在体内实现有效的转导和转基因表达。使用这种方法,能够穿越BBB的静脉注射rAAV变体的剂量可降低100倍,在脑实质中实现显著的转基因表达,同时减少外周转导。此外,该策略可用于将不能从血液穿越BBB的rAAV变体递送至选定的脑区。在此,我们提供了一份详细的方案,用于FUS诱导BBB通透性以将rAAV靶向递送至成年小鼠和大鼠的大脑。

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