Généthon, 91000, Evry, France.
Université Paris-Saclay, Université Evry, INSERM, Généthon, Integrare research unit UMR_S951, 91000, Evry, France.
Gene Ther. 2023 Apr;30(3-4):245-254. doi: 10.1038/s41434-020-00218-6. Epub 2021 Jan 17.
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.
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。