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Predicting T‐cell quality during manufacturing through an artificial intelligence‐based integrative multiomics analytical platform

Large‐scale, reproducible manufacturing of therapeutic cells with consistently high quality is vital for translation to clinically effective and widely accessible cell therapies. However, the biological and logistical complexity of manufacturing a living product, including challenges associated with...

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Autores principales: Odeh‐Couvertier, Valerie Y., Dwarshuis, Nathan J., Colonna, Maxwell B., Levine, Bruce L., Edison, Arthur S., Kotanchek, Theresa, Roy, Krishnendu, Torres‐Garcia, Wandaliz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115702/
https://www.ncbi.nlm.nih.gov/pubmed/35600660
http://dx.doi.org/10.1002/btm2.10282
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author Odeh‐Couvertier, Valerie Y.
Dwarshuis, Nathan J.
Colonna, Maxwell B.
Levine, Bruce L.
Edison, Arthur S.
Kotanchek, Theresa
Roy, Krishnendu
Torres‐Garcia, Wandaliz
author_facet Odeh‐Couvertier, Valerie Y.
Dwarshuis, Nathan J.
Colonna, Maxwell B.
Levine, Bruce L.
Edison, Arthur S.
Kotanchek, Theresa
Roy, Krishnendu
Torres‐Garcia, Wandaliz
author_sort Odeh‐Couvertier, Valerie Y.
collection PubMed
description Large‐scale, reproducible manufacturing of therapeutic cells with consistently high quality is vital for translation to clinically effective and widely accessible cell therapies. However, the biological and logistical complexity of manufacturing a living product, including challenges associated with their inherent variability and uncertainties of process parameters, currently make it difficult to achieve predictable cell‐product quality. Using a degradable microscaffold‐based T‐cell process, we developed an artificial intelligence (AI)‐driven experimental‐computational platform to identify a set of critical process parameters and critical quality attributes from heterogeneous, high‐dimensional, time‐dependent multiomics data, measurable during early stages of manufacturing and predictive of end‐of‐manufacturing product quality. Sequential, design‐of‐experiment‐based studies, coupled with an agnostic machine‐learning framework, were used to extract feature combinations from early in‐culture media assessment that were highly predictive of the end‐product CD4/CD8 ratio and total live CD4(+) and CD8(+) naïve and central memory T cells (CD63L(+)CCR7(+)). Our results demonstrate a broadly applicable platform tool to predict end‐product quality and composition from early time point in‐process measurements during therapeutic cell manufacturing.
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spelling pubmed-91157022022-05-20 Predicting T‐cell quality during manufacturing through an artificial intelligence‐based integrative multiomics analytical platform Odeh‐Couvertier, Valerie Y. Dwarshuis, Nathan J. Colonna, Maxwell B. Levine, Bruce L. Edison, Arthur S. Kotanchek, Theresa Roy, Krishnendu Torres‐Garcia, Wandaliz Bioeng Transl Med Research Articles Large‐scale, reproducible manufacturing of therapeutic cells with consistently high quality is vital for translation to clinically effective and widely accessible cell therapies. However, the biological and logistical complexity of manufacturing a living product, including challenges associated with their inherent variability and uncertainties of process parameters, currently make it difficult to achieve predictable cell‐product quality. Using a degradable microscaffold‐based T‐cell process, we developed an artificial intelligence (AI)‐driven experimental‐computational platform to identify a set of critical process parameters and critical quality attributes from heterogeneous, high‐dimensional, time‐dependent multiomics data, measurable during early stages of manufacturing and predictive of end‐of‐manufacturing product quality. Sequential, design‐of‐experiment‐based studies, coupled with an agnostic machine‐learning framework, were used to extract feature combinations from early in‐culture media assessment that were highly predictive of the end‐product CD4/CD8 ratio and total live CD4(+) and CD8(+) naïve and central memory T cells (CD63L(+)CCR7(+)). Our results demonstrate a broadly applicable platform tool to predict end‐product quality and composition from early time point in‐process measurements during therapeutic cell manufacturing. John Wiley & Sons, Inc. 2022-01-04 /pmc/articles/PMC9115702/ /pubmed/35600660 http://dx.doi.org/10.1002/btm2.10282 Text en © 2021 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Odeh‐Couvertier, Valerie Y.
Dwarshuis, Nathan J.
Colonna, Maxwell B.
Levine, Bruce L.
Edison, Arthur S.
Kotanchek, Theresa
Roy, Krishnendu
Torres‐Garcia, Wandaliz
Predicting T‐cell quality during manufacturing through an artificial intelligence‐based integrative multiomics analytical platform
title Predicting T‐cell quality during manufacturing through an artificial intelligence‐based integrative multiomics analytical platform
title_full Predicting T‐cell quality during manufacturing through an artificial intelligence‐based integrative multiomics analytical platform
title_fullStr Predicting T‐cell quality during manufacturing through an artificial intelligence‐based integrative multiomics analytical platform
title_full_unstemmed Predicting T‐cell quality during manufacturing through an artificial intelligence‐based integrative multiomics analytical platform
title_short Predicting T‐cell quality during manufacturing through an artificial intelligence‐based integrative multiomics analytical platform
title_sort predicting t‐cell quality during manufacturing through an artificial intelligence‐based integrative multiomics analytical platform
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115702/
https://www.ncbi.nlm.nih.gov/pubmed/35600660
http://dx.doi.org/10.1002/btm2.10282
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