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开发一种双杂交 AAV 载体,用于内皮细胞靶向表达血管性血友病因子。

Development of a dual hybrid AAV vector for endothelial-targeted expression of von Willebrand factor.

机构信息

Généthon, 91000, Evry, France.

Université Paris-Saclay, Université Evry, INSERM, Généthon, Integrare research unit UMR_S951, 91000, Evry, France.

出版信息

Gene Ther. 2023 Apr;30(3-4):245-254. doi: 10.1038/s41434-020-00218-6. Epub 2021 Jan 17.

DOI:10.1038/s41434-020-00218-6
PMID:33456057
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10113149/
Abstract

Von Willebrand disease (VWD), the most common inherited bleeding disorder in humans, is caused by quantitative or qualitative defects in von Willebrand factor (VWF). VWD represents a potential target for gene therapy applications, as a single treatment could potentially result in a long-term correction of the disease. In recent years, several liver-directed gene therapy approaches have been exploited for VWD, but their efficacy was generally limited by the large size of the VWF transgene and the reduced hemostatic activity of the protein produced from hepatocytes. In this context, we aimed at developing a gene therapy strategy for gene delivery into endothelial cells, the natural site of biosynthesis of VWF. We optimized an endothelial-specific dual hybrid AAV vector, in which the large VWF cDNA was put under the control of an endothelial promoter and correctly reconstituted upon cell transduction by a combination of trans-splicing and homologous recombination mechanisms. In addition, we modified the AAV vector capsid by introducing an endothelial-targeting peptide to improve the efficiency for endothelial-directed gene transfer. This vector platform allowed the reconstitution of full-length VWF transgene both in vitro in human umbilical vein endothelial cells and in vivo in VWD mice, resulting in long-term expression of VWF.

摘要

血管性血友病(VWD)是人类最常见的遗传性出血性疾病,由血管性血友病因子(VWF)的数量或质量缺陷引起。VWD 是基因治疗应用的潜在目标,因为单次治疗可能会长期纠正该疾病。近年来,已经开发了几种针对 VWD 的肝定向基因治疗方法,但它们的疗效通常受到 VWF 转基因的巨大尺寸和肝细胞产生的蛋白质的止血活性降低的限制。在这种情况下,我们旨在开发一种将基因递送到内皮细胞的基因治疗策略,内皮细胞是 VWF 生物合成的天然部位。我们优化了一种内皮特异性双杂交 AAV 载体,其中大的 VWF cDNA 受内皮启动子控制,并通过转剪接和同源重组机制的组合在细胞转导后正确重建。此外,我们通过引入内皮靶向肽修饰了 AAV 载体衣壳,以提高内皮定向基因转移的效率。该载体平台允许全长 VWF 转基因在体外的人脐静脉内皮细胞和体内的 VWD 小鼠中重建,导致 VWF 的长期表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d985/10113149/c30275587260/41434_2020_218_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d985/10113149/e630e338088f/41434_2020_218_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d985/10113149/4b3ba2943a39/41434_2020_218_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d985/10113149/74442d799d23/41434_2020_218_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d985/10113149/c30275587260/41434_2020_218_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d985/10113149/e630e338088f/41434_2020_218_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d985/10113149/4b3ba2943a39/41434_2020_218_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d985/10113149/74442d799d23/41434_2020_218_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d985/10113149/c30275587260/41434_2020_218_Fig4_HTML.jpg

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2
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J Thromb Haemost. 2018 Mar;16(3):592-604. doi: 10.1111/jth.13938. Epub 2018 Jan 31.
3
Rescue of Pompe disease in mice by AAV-mediated liver delivery of secretable acid α-glucosidase.
Int J Nanomedicine. 2025 Jun 19;20:7851-7868. doi: 10.2147/IJN.S530884. eCollection 2025.
4
Exploring AAV-Mediated Gene Therapy for Inner Ear Diseases: from Preclinical Success to Clinical Potential.探索腺相关病毒介导的内耳疾病基因治疗:从临床前成功到临床潜力
Adv Sci (Weinh). 2025 Sep;12(33):e08397. doi: 10.1002/advs.202408397. Epub 2025 Jun 20.
5
Current clinical applications of AAV-mediated gene therapy.腺相关病毒介导的基因治疗的当前临床应用。
Mol Ther. 2025 Jun 4;33(6):2479-2516. doi: 10.1016/j.ymthe.2025.04.045. Epub 2025 May 5.
6
The future of siRNA-mediated approaches to treat von Willebrand disease.用于治疗血管性血友病的小干扰RNA介导方法的未来。
Expert Rev Hematol. 2025 Feb;18(2):109-122. doi: 10.1080/17474086.2025.2459259. Epub 2025 Jan 29.
7
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Neural Regen Res. 2026 Feb 1;21(2):542-552. doi: 10.4103/NRR.NRR-D-24-00797. Epub 2024 Dec 7.
8
Prospects for gene therapy in polycystic kidney disease.多囊肾病的基因治疗前景。
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9
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10
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10
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