In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA)

The ex-vivo expansion of antigen-specific T-cells for adoptive T-cell immunotherapy requires active interaction between T-cells and antigen-presenting cells therefore culture density and environment become important variables to control. Maintenance of culture density in a static environment is trad...

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Main Authors: Chen, Sixun, Ahmad Amirul Bin Abdul Rahim, Wang, Who-Whong, Cheong, Rachael, Prabhu, Akshaya V., Tan, Jerome Zu Yao, Naing, May Win, Toh, Han Chong, Liu, Dan
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/163363
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spelling sg-ntu-dr.10356-1633632023-12-29T06:51:06Z In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA) Chen, Sixun Ahmad Amirul Bin Abdul Rahim Wang, Who-Whong Cheong, Rachael Prabhu, Akshaya V. Tan, Jerome Zu Yao Naing, May Win Toh, Han Chong Liu, Dan School of Chemical and Biomedical Engineering Bioprocessing Technology Institute, A*STAR Engineering::Bioengineering Bioreactor Epstein Barr Virus The ex-vivo expansion of antigen-specific T-cells for adoptive T-cell immunotherapy requires active interaction between T-cells and antigen-presenting cells therefore culture density and environment become important variables to control. Maintenance of culture density in a static environment is traditionally performed by the expansion of the culture area through splitting of culture from a single vessel into multiple vessels-a highly laborious process. This study aims to validate the use and efficacy of a novel bioreactor, bioreactor with an expandable culture area-dual chamber (BECA-D), that was designed and developed with a cell chamber with expandable culture area (12-108 cm2) and a separate media chamber to allow for in-situ scaling of culture with maintenance of optimum culture density and improved nutrient and gas exchange while minimizing disturbance to the culture. The performance of BECA-D in the culture of Epstein-Barr virus-specific T-cells (EBVSTs) was compared to the 24-well plate. BECA-D had 0.9-9.7 times the average culture yield of the 24-well plates across 5 donor sets. BECA-D was able to maintain the culture environment with relatively stable glucose and lactate levels as the culture expanded. This study concludes that BECA-D can support the culture of ex-vivo EBVSTs with lower manufacturing labour and time requirements compared to the use of the 24-well plate. BECA-D and its adaptation into a closed system with an automated platform (currently being developed) provides cell therapy manufacturers and developers with a closed scale-out solution to producing adoptive cell therapy for clinical use. Agency for Science, Technology and Research (A*STAR) Published version The authors thank Agency for Science Technology and Research (A*STAR), Singapore and National Cancer Centre Singapore for supporting this study and funding support given by A*STAR Industry Alignment Fund— Pre-Positioning Programme (Grant Number: H18/01/a0/022). 2022-12-05T02:44:27Z 2022-12-05T02:44:27Z 2022 Journal Article Chen, S., Ahmad Amirul Bin Abdul Rahim, Wang, W., Cheong, R., Prabhu, A. V., Tan, J. Z. Y., Naing, M. W., Toh, H. C. & Liu, D. (2022). In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA). Scientific Reports, 12(1), 7045-. https://dx.doi.org/10.1038/s41598-022-11015-z 2045-2322 https://hdl.handle.net/10356/163363 10.1038/s41598-022-11015-z 35487951 2-s2.0-85129053719 1 12 7045 en H18/01/a0/022 Scientific Reports © The Author(s) 2022. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Bioengineering
Bioreactor
Epstein Barr Virus
spellingShingle Engineering::Bioengineering
Bioreactor
Epstein Barr Virus
Chen, Sixun
Ahmad Amirul Bin Abdul Rahim
Wang, Who-Whong
Cheong, Rachael
Prabhu, Akshaya V.
Tan, Jerome Zu Yao
Naing, May Win
Toh, Han Chong
Liu, Dan
In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA)
description The ex-vivo expansion of antigen-specific T-cells for adoptive T-cell immunotherapy requires active interaction between T-cells and antigen-presenting cells therefore culture density and environment become important variables to control. Maintenance of culture density in a static environment is traditionally performed by the expansion of the culture area through splitting of culture from a single vessel into multiple vessels-a highly laborious process. This study aims to validate the use and efficacy of a novel bioreactor, bioreactor with an expandable culture area-dual chamber (BECA-D), that was designed and developed with a cell chamber with expandable culture area (12-108 cm2) and a separate media chamber to allow for in-situ scaling of culture with maintenance of optimum culture density and improved nutrient and gas exchange while minimizing disturbance to the culture. The performance of BECA-D in the culture of Epstein-Barr virus-specific T-cells (EBVSTs) was compared to the 24-well plate. BECA-D had 0.9-9.7 times the average culture yield of the 24-well plates across 5 donor sets. BECA-D was able to maintain the culture environment with relatively stable glucose and lactate levels as the culture expanded. This study concludes that BECA-D can support the culture of ex-vivo EBVSTs with lower manufacturing labour and time requirements compared to the use of the 24-well plate. BECA-D and its adaptation into a closed system with an automated platform (currently being developed) provides cell therapy manufacturers and developers with a closed scale-out solution to producing adoptive cell therapy for clinical use.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Chen, Sixun
Ahmad Amirul Bin Abdul Rahim
Wang, Who-Whong
Cheong, Rachael
Prabhu, Akshaya V.
Tan, Jerome Zu Yao
Naing, May Win
Toh, Han Chong
Liu, Dan
format Article
author Chen, Sixun
Ahmad Amirul Bin Abdul Rahim
Wang, Who-Whong
Cheong, Rachael
Prabhu, Akshaya V.
Tan, Jerome Zu Yao
Naing, May Win
Toh, Han Chong
Liu, Dan
author_sort Chen, Sixun
title In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA)
title_short In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA)
title_full In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA)
title_fullStr In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA)
title_full_unstemmed In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA)
title_sort in-situ scalable manufacturing of epstein-barr virus-specific t-cells using bioreactor with an expandable culture area (beca)
publishDate 2022
url https://hdl.handle.net/10356/163363
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