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Empty virions in AAV8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects
Empty virions are inadvertent by-products of recombinant adeno-associated virus (rAAV) packaging process, resulting in vector lots with mixtures of full and empty virions at variable ratios. Impact of empty virions on the efficiency and side effects of rAAV transduction has not been well characteriz...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255953/ https://www.ncbi.nlm.nih.gov/pubmed/25485285 http://dx.doi.org/10.1038/mtm.2013.9 |
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author | Gao, Kai Li, Mengxin Zhong, Li Su, Qin Li, Jia Li, Shaoyong He, Ran Zhang, Yu Hendricks, Gregory Wang, Junzhi Gao, Guangping |
author_facet | Gao, Kai Li, Mengxin Zhong, Li Su, Qin Li, Jia Li, Shaoyong He, Ran Zhang, Yu Hendricks, Gregory Wang, Junzhi Gao, Guangping |
author_sort | Gao, Kai |
collection | PubMed |
description | Empty virions are inadvertent by-products of recombinant adeno-associated virus (rAAV) packaging process, resulting in vector lots with mixtures of full and empty virions at variable ratios. Impact of empty virions on the efficiency and side effects of rAAV transduction has not been well characterized. Here, we generated partially and completely empty AAV8 virions, fully packaged rAAV8 lots, and mixtures of empty and fully packaged virions with variable ratios of empty virions. The aforementioned dosing formulations of rAAV8 expressing either cellular (EGFP (enhanced green fluorescent protein) or nuclear-targeted (n) LacZ) or secreted (human α1-antitrypsin (hA1AT)) reporter genes were intravenously injected into two different mouse strains, followed by analyses of transgene expressions and serum alanine aminotransferase (ALT) levels at different time points. We found that addition of empty particles to the fixed doses of rAAV8 preparations repressed liver transduction up to 64% (serum hA1AT) and 44% (nLacZ) in C57BL/6 mice, respectively. The similar trend in inhibiting EGFP expression together with concurrent elevations of serum ALT levels were observed in the BALB/c mice, indicating that empty particles may also exacerbate side effects of rAAV8 EGFP transduction. Our results suggest that removal of empty particles from rAAV preparations may improve efficacy and safety of AAV in clinical applications. |
format | Online Article Text |
id | pubmed-4255953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42559532014-12-04 Empty virions in AAV8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects Gao, Kai Li, Mengxin Zhong, Li Su, Qin Li, Jia Li, Shaoyong He, Ran Zhang, Yu Hendricks, Gregory Wang, Junzhi Gao, Guangping Mol Ther Methods Clin Dev Article Empty virions are inadvertent by-products of recombinant adeno-associated virus (rAAV) packaging process, resulting in vector lots with mixtures of full and empty virions at variable ratios. Impact of empty virions on the efficiency and side effects of rAAV transduction has not been well characterized. Here, we generated partially and completely empty AAV8 virions, fully packaged rAAV8 lots, and mixtures of empty and fully packaged virions with variable ratios of empty virions. The aforementioned dosing formulations of rAAV8 expressing either cellular (EGFP (enhanced green fluorescent protein) or nuclear-targeted (n) LacZ) or secreted (human α1-antitrypsin (hA1AT)) reporter genes were intravenously injected into two different mouse strains, followed by analyses of transgene expressions and serum alanine aminotransferase (ALT) levels at different time points. We found that addition of empty particles to the fixed doses of rAAV8 preparations repressed liver transduction up to 64% (serum hA1AT) and 44% (nLacZ) in C57BL/6 mice, respectively. The similar trend in inhibiting EGFP expression together with concurrent elevations of serum ALT levels were observed in the BALB/c mice, indicating that empty particles may also exacerbate side effects of rAAV8 EGFP transduction. Our results suggest that removal of empty particles from rAAV preparations may improve efficacy and safety of AAV in clinical applications. Nature Publishing Group 2014-01-29 /pmc/articles/PMC4255953/ /pubmed/25485285 http://dx.doi.org/10.1038/mtm.2013.9 Text en Copyright © 2014 American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution Upported 3.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/deed.en_US |
spellingShingle | Article Gao, Kai Li, Mengxin Zhong, Li Su, Qin Li, Jia Li, Shaoyong He, Ran Zhang, Yu Hendricks, Gregory Wang, Junzhi Gao, Guangping Empty virions in AAV8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects |
title | Empty virions in AAV8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects |
title_full | Empty virions in AAV8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects |
title_fullStr | Empty virions in AAV8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects |
title_full_unstemmed | Empty virions in AAV8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects |
title_short | Empty virions in AAV8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects |
title_sort | empty virions in aav8 vector preparations reduce transduction efficiency and may cause total viral particle dose-limiting side effects |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255953/ https://www.ncbi.nlm.nih.gov/pubmed/25485285 http://dx.doi.org/10.1038/mtm.2013.9 |
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