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A Comprehensive Map of CNS Transduction by Eight Recombinant Adeno-associated Virus Serotypes Upon Cerebrospinal Fluid Administration in Pigs
Authors:Nicolina Cristina Sorrentino  Veronica Maffia  Sandra Strollo  Vincenzo Cacace  Noemi Romagnoli  Anna Manfredi  Domenico Ventrella  Francesco Dondi  Francesca Barone  Massimo Giunti  Anne-Renee Graham  Yan Huang  Susan L Kalled  Alberto Auricchio  Maria Laura Bacci  Enrico Maria Surace  Alessandro Fraldi
Affiliation:1.Telethon Institute of Genetics and Medicine (TIGEM), Naples, Italy;2.Department of Veterinary Medical Sciences (DIMEVET), University of Bologna, Bologna, Italy;3.Shire, Discovery Biology and Translational Research, Lexington, Massachusetts, USA;4.Medical Genetics, Department of Translational Medicine, “FEDERICO II” University, Naples, Italy
Abstract:
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been demonstrated to be effective in delivering therapeutic genes to the central nervous system (CNS) in different disease animal models. However, a quantitative and qualitative analysis of transduction patterns of the most promising rAAV serotypes for brain targeting in large animal models is missing. Here, we characterize distribution, transduction efficiency, and cellular targeting of rAAV serotypes 1, 2, 5, 7, 9, rh.10, rh.39, and rh.43 delivered into the cisterna magna of wild-type pigs. rAAV9 showed the highest transduction efficiency and the widest distribution capability among the vectors tested. Moreover, rAAV9 robustly transduced both glia and neurons, including the motor neurons of the spinal cord. Relevant cell transduction specificity of the glia was observed after rAAV1 and rAAV7 delivery. rAAV7 also displayed a specific tropism to Purkinje cells. Evaluation of biochemical and hematological markers suggested that all rAAV serotypes tested were well tolerated. This study provides a comprehensive CNS transduction map in a useful preclinical large animal model enabling the selection of potentially clinically transferable rAAV serotypes based on disease specificity. Therefore, our data are instrumental for the clinical evaluation of these rAAV vectors in human neurodegenerative diseases.
Keywords:
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