MRI-Guided Focused Ultrasound for Targeted Delivery of rAAV to the Brain
Authors:
Open Access
- 20 February 2019
- book chapter
- Published by Springer Nature
- Vol. 1950, 177-197
Abstract
Recombinant adeno-associated viral (rAAV) vectors are a promising tool for therapeutic gene delivery to the brain. However, the delivery of rAAVs across the blood-brain barrier (BBB) and entry into the brain remains a major challenge for rAAV-based gene therapy. To circumvent this limitation, transcranial MRI-guided focused ultrasound (MRIgFUS) combined with intravenously injected microbubbles has been used to transiently and reversibly increase BBB permeability in targeted brain regions. Systemic administration of rAAVs at the time of sonication with focused ultrasound (FUS) facilitates the passage of rAAVs through the BBB and into the brain parenchyma. We and others have demonstrated that FUS-mediated rAAV delivery to the brain results in efficient transduction and transgene expression in vivo. Using this approach, the dose of intravenously injected rAAV variants that can cross the BBB can be reduced by 100 times, achieving significant transgene expression in the brain parenchyma with reduced peripheral transduction. Moreover, this strategy can be used to deliver rAAV variants that do not cross the BBB from the blood to selected brain regions. Here, we provide a detailed protocol for FUS-induced BBB permeability for targeted rAAV delivery to the brain of adult mice and rats.Keywords
This publication has 47 references indexed in Scilit:
- Gene therapy comes of ageScience, 2018
- Neurodegeneration: the first mechanistic therapy and other progress in 2017The Lancet Neurology, 2018
- 2017 Was the Year We Have Been Waiting ForHuman Gene Therapy Clinical Development, 2017
- Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systemsNature Neuroscience, 2017
- Clinical development of gene therapy: results and lessons from recent successesMolecular Therapy - Methods & Clinical Development, 2016
- AAV9: Over the Fence and Into the Woods …Molecular Therapy, 2011
- RETRACTED ARTICLE: Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMNNature Biotechnology, 2010
- Viral vectors for neurotrophic factor delivery: A gene therapy approach for neurodegenerative diseases of the CNSPharmacological Research, 2010
- AAV9: a potential blood-brain barrier busterMolecular Therapy, 2009
- Gene therapy in the CNSGene Therapy, 2000