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Large-scale production of lentiviral vector in a closed system hollow fiber bioreactor

Lentiviral vectors are widely used in the field of gene therapy as an effective method for permanent gene delivery. While current methods of producing small scale vector batches for research purposes depend largely on culture flasks, the emergence and popularity of lentiviral vectors in translationa...

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Autores principales: Sheu, Jonathan, Beltzer, Jim, Fury, Brian, Wilczek, Katarzyna, Tobin, Steve, Falconer, Danny, Nolta, Jan, Bauer, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470365/
https://www.ncbi.nlm.nih.gov/pubmed/26151065
http://dx.doi.org/10.1038/mtm.2015.20
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author Sheu, Jonathan
Beltzer, Jim
Fury, Brian
Wilczek, Katarzyna
Tobin, Steve
Falconer, Danny
Nolta, Jan
Bauer, Gerhard
author_facet Sheu, Jonathan
Beltzer, Jim
Fury, Brian
Wilczek, Katarzyna
Tobin, Steve
Falconer, Danny
Nolta, Jan
Bauer, Gerhard
author_sort Sheu, Jonathan
collection PubMed
description Lentiviral vectors are widely used in the field of gene therapy as an effective method for permanent gene delivery. While current methods of producing small scale vector batches for research purposes depend largely on culture flasks, the emergence and popularity of lentiviral vectors in translational, preclinical and clinical research has demanded their production on a much larger scale, a task that can be difficult to manage with the numbers of producer cell culture flasks required for large volumes of vector. To generate a large scale, partially closed system method for the manufacturing of clinical grade lentiviral vector suitable for the generation of induced pluripotent stem cells (iPSCs), we developed a method employing a hollow fiber bioreactor traditionally used for cell expansion. We have demonstrated the growth, transfection, and vector-producing capability of 293T producer cells in this system. Vector particle RNA titers after subsequent vector concentration yielded values comparable to lentiviral iPSC induction vector batches produced using traditional culture methods in 225 cm(2) flasks (T225s) and in 10-layer cell factories (CF10s), while yielding a volume nearly 145 times larger than the yield from a T225 flask and nearly three times larger than the yield from a CF10. Employing a closed system hollow fiber bioreactor for vector production offers the possibility of manufacturing large quantities of gene therapy vector while minimizing reagent usage, equipment footprint, and open system manipulation.
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spelling pubmed-44703652015-07-06 Large-scale production of lentiviral vector in a closed system hollow fiber bioreactor Sheu, Jonathan Beltzer, Jim Fury, Brian Wilczek, Katarzyna Tobin, Steve Falconer, Danny Nolta, Jan Bauer, Gerhard Mol Ther Methods Clin Dev Article Lentiviral vectors are widely used in the field of gene therapy as an effective method for permanent gene delivery. While current methods of producing small scale vector batches for research purposes depend largely on culture flasks, the emergence and popularity of lentiviral vectors in translational, preclinical and clinical research has demanded their production on a much larger scale, a task that can be difficult to manage with the numbers of producer cell culture flasks required for large volumes of vector. To generate a large scale, partially closed system method for the manufacturing of clinical grade lentiviral vector suitable for the generation of induced pluripotent stem cells (iPSCs), we developed a method employing a hollow fiber bioreactor traditionally used for cell expansion. We have demonstrated the growth, transfection, and vector-producing capability of 293T producer cells in this system. Vector particle RNA titers after subsequent vector concentration yielded values comparable to lentiviral iPSC induction vector batches produced using traditional culture methods in 225 cm(2) flasks (T225s) and in 10-layer cell factories (CF10s), while yielding a volume nearly 145 times larger than the yield from a T225 flask and nearly three times larger than the yield from a CF10. Employing a closed system hollow fiber bioreactor for vector production offers the possibility of manufacturing large quantities of gene therapy vector while minimizing reagent usage, equipment footprint, and open system manipulation. Nature Publishing Group 2015-06-17 /pmc/articles/PMC4470365/ /pubmed/26151065 http://dx.doi.org/10.1038/mtm.2015.20 Text en Copyright © 2015 American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Article
Sheu, Jonathan
Beltzer, Jim
Fury, Brian
Wilczek, Katarzyna
Tobin, Steve
Falconer, Danny
Nolta, Jan
Bauer, Gerhard
Large-scale production of lentiviral vector in a closed system hollow fiber bioreactor
title Large-scale production of lentiviral vector in a closed system hollow fiber bioreactor
title_full Large-scale production of lentiviral vector in a closed system hollow fiber bioreactor
title_fullStr Large-scale production of lentiviral vector in a closed system hollow fiber bioreactor
title_full_unstemmed Large-scale production of lentiviral vector in a closed system hollow fiber bioreactor
title_short Large-scale production of lentiviral vector in a closed system hollow fiber bioreactor
title_sort large-scale production of lentiviral vector in a closed system hollow fiber bioreactor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470365/
https://www.ncbi.nlm.nih.gov/pubmed/26151065
http://dx.doi.org/10.1038/mtm.2015.20
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