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Transduction patterns in the CNS following various routes of AAV-5-mediated gene delivery

Authors :
K. L. Pietersz
Gerard J.M. Martens
S. M. Pouw
Jacek Lubelski
M. S. Baatje
Raygene Martier
Pavlina Konstantinova
Harald Petry
Cynthia Brouwers
L. Fokkert
S. J. van Deventer
Jolanda M. Liefhebber
Bas Blits
Source :
Gene Therapy, 28, 435-446, Gene Therapy, 28, pp. 435-446, Gene Therapy, 28, 435-446. NATURE PUBLISHING GROUP
Publication Year :
2020
Publisher :
NATURE PUBLISHING GROUP, 2020.

Abstract

Various administration routes of adeno-associated virus (AAV)-based gene therapy have been examined to target the central nervous system to answer the question what the most optimal delivery route is for treatment of the brain with certain indications. In this study, we evaluated AAV5 vector system for its capability to target the central nervous system via intrastriatal, intrathalamic or intracerebroventricular delivery routes in rats. AAV5 is an ideal candidate for gene therapy because of its relatively low level of existing neutralizing antibodies compared to other serotypes, and its broad tissue and cell tropism. Intrastriatal administration of AAV5-GFP resulted in centralized localized vector distribution and expression in the frontal part of the brain. Intrathalamic injection showed transduction and gradient expression from the rostral brain into lumbar spinal cord, while intracerebroventricular administration led to a more evenly, albeit relatively superficially distributed, transduction and expression throughout the central nervous system. To visualize the differences between localized and intra-cerebral spinal fluid administration routes, we compared intrastriatal to intracerebroventricular and intrathecal administration of AAV5-GFP. Together, our results demonstrate that for efficient transgene expression, various administration routes can be applied.

Details

Language :
English
ISSN :
09697128
Database :
OpenAIRE
Journal :
Gene Therapy, 28, 435-446, Gene Therapy, 28, pp. 435-446, Gene Therapy, 28, 435-446. NATURE PUBLISHING GROUP
Accession number :
edsair.doi.dedup.....dcf0ba16db097f75341f07d80cc01142