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Novel biomanufacturing platform for large-scale and high-quality human T cells production
The adoptive transfer of human T cells or genetically-engineered T cells with cancer-targeting receptors has shown tremendous promise for eradicating tumors in clinical trials. The objective of this study was to develop a novel T cell biomanufacturing platform using stirred-tank bioreactor for large...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480708/ https://www.ncbi.nlm.nih.gov/pubmed/31044002 http://dx.doi.org/10.1186/s13036-019-0167-2 |
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author | Ou, Jianfa Si, Yingnan Tang, Yawen Salzer, Grace E. Lu, Yun Kim, Seulhee Qin, Hongwei Zhou, Lufang Liu, Xiaoguang |
author_facet | Ou, Jianfa Si, Yingnan Tang, Yawen Salzer, Grace E. Lu, Yun Kim, Seulhee Qin, Hongwei Zhou, Lufang Liu, Xiaoguang |
author_sort | Ou, Jianfa |
collection | PubMed |
description | The adoptive transfer of human T cells or genetically-engineered T cells with cancer-targeting receptors has shown tremendous promise for eradicating tumors in clinical trials. The objective of this study was to develop a novel T cell biomanufacturing platform using stirred-tank bioreactor for large-scale and high-quality cellular production. First, various factors, such as bioreactor parameters, media, supplements, stimulation, seed age, and donors, were investigated. A serum-free fed-batch bioproduction process was developed to achieve 1000-fold expansion within 8 days after first stimulation and another 500-fold expansion with second stimulation. Second, this biomanufacturing process was successfully scaled up in bioreactor with dilution factor of 10, and the robustness and reproducibility of the process was confirmed by the inclusion of different donors’ T cells of various qualities. Finally, T cell quality was monitored using 12 surface markers and 3 intracellular cytokines as the critical quality assessment criteria in early, middle and late stages of cell production. In this study, a new biomanufacturing platform was created to produce reliable, reproducible, high-quality, and large-quantity (i.e. > 5 billion) human T cells in stirred-tank bioreactor. This platform is compatible with the production systems of monoclonal antibodies, vaccines, and other therapeutic cells, which provides not only the proof-of-concept but also the ready-to-use new approach of T cell expansion for clinical immune therapy. |
format | Online Article Text |
id | pubmed-6480708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64807082019-05-01 Novel biomanufacturing platform for large-scale and high-quality human T cells production Ou, Jianfa Si, Yingnan Tang, Yawen Salzer, Grace E. Lu, Yun Kim, Seulhee Qin, Hongwei Zhou, Lufang Liu, Xiaoguang J Biol Eng Research The adoptive transfer of human T cells or genetically-engineered T cells with cancer-targeting receptors has shown tremendous promise for eradicating tumors in clinical trials. The objective of this study was to develop a novel T cell biomanufacturing platform using stirred-tank bioreactor for large-scale and high-quality cellular production. First, various factors, such as bioreactor parameters, media, supplements, stimulation, seed age, and donors, were investigated. A serum-free fed-batch bioproduction process was developed to achieve 1000-fold expansion within 8 days after first stimulation and another 500-fold expansion with second stimulation. Second, this biomanufacturing process was successfully scaled up in bioreactor with dilution factor of 10, and the robustness and reproducibility of the process was confirmed by the inclusion of different donors’ T cells of various qualities. Finally, T cell quality was monitored using 12 surface markers and 3 intracellular cytokines as the critical quality assessment criteria in early, middle and late stages of cell production. In this study, a new biomanufacturing platform was created to produce reliable, reproducible, high-quality, and large-quantity (i.e. > 5 billion) human T cells in stirred-tank bioreactor. This platform is compatible with the production systems of monoclonal antibodies, vaccines, and other therapeutic cells, which provides not only the proof-of-concept but also the ready-to-use new approach of T cell expansion for clinical immune therapy. BioMed Central 2019-04-23 /pmc/articles/PMC6480708/ /pubmed/31044002 http://dx.doi.org/10.1186/s13036-019-0167-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ou, Jianfa Si, Yingnan Tang, Yawen Salzer, Grace E. Lu, Yun Kim, Seulhee Qin, Hongwei Zhou, Lufang Liu, Xiaoguang Novel biomanufacturing platform for large-scale and high-quality human T cells production |
title | Novel biomanufacturing platform for large-scale and high-quality human T cells production |
title_full | Novel biomanufacturing platform for large-scale and high-quality human T cells production |
title_fullStr | Novel biomanufacturing platform for large-scale and high-quality human T cells production |
title_full_unstemmed | Novel biomanufacturing platform for large-scale and high-quality human T cells production |
title_short | Novel biomanufacturing platform for large-scale and high-quality human T cells production |
title_sort | novel biomanufacturing platform for large-scale and high-quality human t cells production |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480708/ https://www.ncbi.nlm.nih.gov/pubmed/31044002 http://dx.doi.org/10.1186/s13036-019-0167-2 |
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