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Production of adeno-associated virus (AAV) serotypes by transient transfection of HEK293 cell suspension cultures for gene delivery

Adeno-associated virus (AAV) is being used successfully in gene therapy. Different serotypes of AAV target specific organs and tissues with high efficiency. There exists an increasing demand to manufacture various AAV serotypes in large quantities for pre-clinical and clinical trials. A generic and...

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Autores principales: Chahal, Parminder Singh, Schulze, Erica, Tran, Rosa, Montes, Johnny, Kamen, Amine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113661/
https://www.ncbi.nlm.nih.gov/pubmed/24239634
http://dx.doi.org/10.1016/j.jviromet.2013.10.038
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author Chahal, Parminder Singh
Schulze, Erica
Tran, Rosa
Montes, Johnny
Kamen, Amine A.
author_facet Chahal, Parminder Singh
Schulze, Erica
Tran, Rosa
Montes, Johnny
Kamen, Amine A.
author_sort Chahal, Parminder Singh
collection PubMed
description Adeno-associated virus (AAV) is being used successfully in gene therapy. Different serotypes of AAV target specific organs and tissues with high efficiency. There exists an increasing demand to manufacture various AAV serotypes in large quantities for pre-clinical and clinical trials. A generic and scalable method has been described in this study to efficiently produce AAV serotypes (AAV1-9) by transfection of a fully characterized cGMP HEK293SF cell line grown in suspension and serum-free medium. First, the production parameters were evaluated using AAV2 as a model serotype. Second, all nine AAV serotypes were produced successfully with yields of 10(13) Vg/L cell culture. Subsequently, AAV2 and AAV6 serotypes were produced in 3-L controlled bioreactors where productions yielded up to 10(13) Vg/L similar to the yields obtained in shake-flasks. For example, for AAV2 10(13) Vg/L cell culture (6.8 × 10(11) IVP/L) were measured between 48 and 64 h post transfection (hpt). During this period, the average cell specific AAV2 yields of 6800 Vg per cell and 460 IVP per cell were obtained with a Vg to IVP ratio of less than 20. Successful operations in bioreactors demonstrated the potential for scale-up and industrialization of this generic process for manufacturing AAV serotypes efficiently.
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spelling pubmed-71136612020-04-02 Production of adeno-associated virus (AAV) serotypes by transient transfection of HEK293 cell suspension cultures for gene delivery Chahal, Parminder Singh Schulze, Erica Tran, Rosa Montes, Johnny Kamen, Amine A. J Virol Methods Article Adeno-associated virus (AAV) is being used successfully in gene therapy. Different serotypes of AAV target specific organs and tissues with high efficiency. There exists an increasing demand to manufacture various AAV serotypes in large quantities for pre-clinical and clinical trials. A generic and scalable method has been described in this study to efficiently produce AAV serotypes (AAV1-9) by transfection of a fully characterized cGMP HEK293SF cell line grown in suspension and serum-free medium. First, the production parameters were evaluated using AAV2 as a model serotype. Second, all nine AAV serotypes were produced successfully with yields of 10(13) Vg/L cell culture. Subsequently, AAV2 and AAV6 serotypes were produced in 3-L controlled bioreactors where productions yielded up to 10(13) Vg/L similar to the yields obtained in shake-flasks. For example, for AAV2 10(13) Vg/L cell culture (6.8 × 10(11) IVP/L) were measured between 48 and 64 h post transfection (hpt). During this period, the average cell specific AAV2 yields of 6800 Vg per cell and 460 IVP per cell were obtained with a Vg to IVP ratio of less than 20. Successful operations in bioreactors demonstrated the potential for scale-up and industrialization of this generic process for manufacturing AAV serotypes efficiently. Published by Elsevier B.V. 2014-02 2013-11-13 /pmc/articles/PMC7113661/ /pubmed/24239634 http://dx.doi.org/10.1016/j.jviromet.2013.10.038 Text en Crown copyright © 2013 Published by Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Chahal, Parminder Singh
Schulze, Erica
Tran, Rosa
Montes, Johnny
Kamen, Amine A.
Production of adeno-associated virus (AAV) serotypes by transient transfection of HEK293 cell suspension cultures for gene delivery
title Production of adeno-associated virus (AAV) serotypes by transient transfection of HEK293 cell suspension cultures for gene delivery
title_full Production of adeno-associated virus (AAV) serotypes by transient transfection of HEK293 cell suspension cultures for gene delivery
title_fullStr Production of adeno-associated virus (AAV) serotypes by transient transfection of HEK293 cell suspension cultures for gene delivery
title_full_unstemmed Production of adeno-associated virus (AAV) serotypes by transient transfection of HEK293 cell suspension cultures for gene delivery
title_short Production of adeno-associated virus (AAV) serotypes by transient transfection of HEK293 cell suspension cultures for gene delivery
title_sort production of adeno-associated virus (aav) serotypes by transient transfection of hek293 cell suspension cultures for gene delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113661/
https://www.ncbi.nlm.nih.gov/pubmed/24239634
http://dx.doi.org/10.1016/j.jviromet.2013.10.038
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