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单次增强型脑脊液内递送后,靶向递送至非人类灵长类动物小脑的 AAV5-GFP 的可行性。

Feasibility of Targeted Delivery of AAV5-GFP into the Cerebellum of Nonhuman Primates Following a Single Convection-Enhanced Delivery Infusion.

机构信息

Valley Biosystems, Inc., West Sacramento, California, USA.

出版信息

Hum Gene Ther. 2022 Jan;33(1-2):86-93. doi: 10.1089/hum.2021.163. Epub 2022 Jan 3.

DOI:10.1089/hum.2021.163
PMID:34779239
Abstract

In this study, we built upon our previous work to demonstrate the distribution and transport of AAV5-green fluorescent protein (GFP) following a single convection-enhanced delivery infusion into the nonhuman primate cerebellum, with no untoward side effects noted. Dosing under magnetic resonance imaging guidance revealed a sixfold larger volume of distribution compared with the volume of infusion, with no evidence of reflux underscoring the convective properties of the cerebellum and step design of the cannula. Postmortem tissue analysis, 4 weeks post-adeno-associated viral (AAV) delivery, revealed the robust presence of the transgene , with GFP detection in secondary regions not directly targeted by the infusion, denoting distal transport of the vector. Irrespective of tropism, a twofold larger area of transgene expression was found and was corroborated against the presence of contrast on T1-weighted images. Different levels of transduction were detected between animals, which were negatively correlated with the level of antibody titer against the GFP construct, whereby the higher the antibody titer, the lower the level of transgene expression. These findings support the use of the posterior fossa as a potential target site for direct delivery of gene-based therapeutics for cerebellar diseases.

摘要

在这项研究中,我们在前人的工作基础上,证明了在非人类灵长类动物小脑单次增强传递输注后,AAV5-绿色荧光蛋白(GFP)的分布和传递,未观察到不良副作用。磁共振成像引导下的给药显示,与输注体积相比,分布体积大了六倍,没有证据表明回流,这突出了小脑的对流特性和套管的台阶设计。腺相关病毒(AAV)给药后 4 周的尸检组织分析显示,转基因的存在非常活跃,在未直接接受输注的次级区域检测到 GFP,表明载体的远距离运输。无论亲嗜性如何,都发现转基因表达面积增加了两倍,并与 T1 加权图像上的对比存在相吻合。不同动物之间的转导水平存在差异,这与针对 GFP 构建体的抗体滴度呈负相关,抗体滴度越高,转基因表达水平越低。这些发现支持将后颅窝作为小脑疾病基因治疗的直接靶向传递的潜在靶位。

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ACS Nano. 2024 Jul 9;18(27):17869-17881. doi: 10.1021/acsnano.4c04159. Epub 2024 Jun 26.
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Pre-clinical delivery of gene therapy products to the cerebrospinal fluid: challenges and considerations for clinical translation.基因治疗产品向脑脊液的临床前递送:临床转化的挑战与考量
Front Mol Neurosci. 2023 Aug 17;16:1248271. doi: 10.3389/fnmol.2023.1248271. eCollection 2023.
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AAV-based in vivo gene therapy for neurological disorders.
基于腺相关病毒的神经疾病体内基因治疗。
Nat Rev Drug Discov. 2023 Oct;22(10):789-806. doi: 10.1038/s41573-023-00766-7. Epub 2023 Sep 1.