Development of a dual hybrid AAV vector for endothelial-targeted expression of von Willebrand factor.
Elena BarbonCharlotte KaweckiSolenne MarmierAboud SakkalFanny CollaudSeverine CharlesGiuseppe RonzittiCaterina CasariOlivier D ChristopheCecile V DenisPeter J LentingFederico MingozziPublished in: Gene therapy (2021)
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.
Keyphrases
- gene therapy
- endothelial cells
- high glucose
- dna damage
- poor prognosis
- vascular endothelial growth factor
- dna methylation
- gene expression
- type diabetes
- dna repair
- high throughput
- cell therapy
- high resolution
- systematic review
- single cell
- climate change
- metabolic syndrome
- atrial fibrillation
- drug delivery
- mesenchymal stem cells
- skeletal muscle
- replacement therapy
- genome wide identification