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A comprehensive study of a 29-capsid AAV library in a non-human primate central nervous system.

Authors :
Kondratov O
Kondratova L
Mandel RJ
Coleman K
Savage MA
Gray-Edwards HL
Ness TJ
Rodriguez-Lebron E
Bell RD
Rabinowitz J
Gamlin PD
Zolotukhin S
Source :
Molecular therapy : the journal of the American Society of Gene Therapy [Mol Ther] 2021 Sep 01; Vol. 29 (9), pp. 2806-2820. Date of Electronic Publication: 2021 Jul 21.
Publication Year :
2021

Abstract

Non-human primates (NHPs) are a preferred animal model for optimizing adeno-associated virus (AAV)-mediated CNS gene delivery protocols before clinical trials. In spite of its inherent appeal, it is challenging to compare different serotypes, delivery routes, and disease indications in a well-powered, comprehensive, multigroup NHP experiment. Here, a multiplex barcode recombinant AAV (rAAV) vector-tracing strategy has been applied to a systemic analysis of 29 distinct, wild-type (WT), AAV natural isolates and engineered capsids in the CNS of eight macaques. The report describes distribution of each capsid in 15 areas of the macaques' CNS after intraparenchymal (putamen) injection, or cerebrospinal fluid (CSF)-mediated administration routes (intracisternal, intrathecal, or intracerebroventricular). To trace the vector biodistribution (viral DNA) and targeted tissues transduction (viral mRNA) of each capsid in each of the analyzed CNS areas, quantitative next-generation sequencing analysis, assisted by the digital-droplet PCR technology, was used. The report describes the most efficient AAV capsid variants targeting specific CNS areas after each route of administration using the direct side-by-side comparison of WT AAV isolates and a new generation of rationally designed capsids. The newly developed bioinformatics and visualization algorithms, applicable to the comparative analysis of several mammalian brain models, have been developed and made available in the public domain.<br />Competing Interests: Declaration of interests At the time of project design and implementation, R.D.B and J.R. were employees of Pfizer, whereas E.R.-L. is currently an employee of Lacerta Therapeutics Inc. Aspects of this work were funded by Pfizer and Lacerta Therapeutics Inc. R.J.M., S.Z., and E.R.-L. are co-founders and shareholders of Lacerta Therapeutics Inc.<br /> (Copyright © 2021 The American Society of Gene and Cell Therapy. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1525-0024
Volume :
29
Issue :
9
Database :
MEDLINE
Journal :
Molecular therapy : the journal of the American Society of Gene Therapy
Publication Type :
Academic Journal
Accession number :
34298128
Full Text :
https://doi.org/10.1016/j.ymthe.2021.07.010