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Needle to needle robot‐assisted manufacture of cell therapy products

Advanced therapeutic medicinal products (ATMPs) have emerged as novel therapies for untreatable diseases, generating the need for large volumes of high‐quality, clinically‐compliant GMP cells to replace costly, high‐risk and limited scale manual expansion processes. We present the design of a fully...

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Autores principales: Ochs, Jelena, Hanga, Mariana P., Shaw, Georgina, Duffy, Niamh, Kulik, Michael, Tissin, Nokilaj, Reibert, Daniel, Biermann, Ferdinand, Moutsatsou, Panagiota, Ratnayake, Shibani, Nienow, Alvin, Koenig, Niels, Schmitt, Robert, Rafiq, Qasim, Hewitt, Christopher J., Barry, Frank, Murphy, J. Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472012/
https://www.ncbi.nlm.nih.gov/pubmed/36176619
http://dx.doi.org/10.1002/btm2.10387
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author Ochs, Jelena
Hanga, Mariana P.
Shaw, Georgina
Duffy, Niamh
Kulik, Michael
Tissin, Nokilaj
Reibert, Daniel
Biermann, Ferdinand
Moutsatsou, Panagiota
Ratnayake, Shibani
Nienow, Alvin
Koenig, Niels
Schmitt, Robert
Rafiq, Qasim
Hewitt, Christopher J.
Barry, Frank
Murphy, J. Mary
author_facet Ochs, Jelena
Hanga, Mariana P.
Shaw, Georgina
Duffy, Niamh
Kulik, Michael
Tissin, Nokilaj
Reibert, Daniel
Biermann, Ferdinand
Moutsatsou, Panagiota
Ratnayake, Shibani
Nienow, Alvin
Koenig, Niels
Schmitt, Robert
Rafiq, Qasim
Hewitt, Christopher J.
Barry, Frank
Murphy, J. Mary
author_sort Ochs, Jelena
collection PubMed
description Advanced therapeutic medicinal products (ATMPs) have emerged as novel therapies for untreatable diseases, generating the need for large volumes of high‐quality, clinically‐compliant GMP cells to replace costly, high‐risk and limited scale manual expansion processes. We present the design of a fully automated, robot‐assisted platform incorporating the use of multiliter stirred tank bioreactors for scalable production of adherent human stem cells. The design addresses a needle‐to‐needle closed process incorporating automated bone marrow collection, cell isolation, expansion, and collection into cryovials for patient delivery. AUTOSTEM, a modular, adaptable, fully closed system ensures no direct operator interaction with biological material; all commands are performed through a graphic interface. Seeding of source material, process monitoring, feeding, sampling, harvesting and cryopreservation are automated within the closed platform, comprising two clean room levels enabling both open and closed processes. A bioprocess based on human MSCs expanded on microcarriers was used for proof of concept. Utilizing equivalent culture parameters, the AUTOSTEM robot‐assisted platform successfully performed cell expansion at the liter scale, generating results comparable to manual production, while maintaining cell quality postprocessing.
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spelling pubmed-94720122022-09-28 Needle to needle robot‐assisted manufacture of cell therapy products Ochs, Jelena Hanga, Mariana P. Shaw, Georgina Duffy, Niamh Kulik, Michael Tissin, Nokilaj Reibert, Daniel Biermann, Ferdinand Moutsatsou, Panagiota Ratnayake, Shibani Nienow, Alvin Koenig, Niels Schmitt, Robert Rafiq, Qasim Hewitt, Christopher J. Barry, Frank Murphy, J. Mary Bioeng Transl Med Research Articles Advanced therapeutic medicinal products (ATMPs) have emerged as novel therapies for untreatable diseases, generating the need for large volumes of high‐quality, clinically‐compliant GMP cells to replace costly, high‐risk and limited scale manual expansion processes. We present the design of a fully automated, robot‐assisted platform incorporating the use of multiliter stirred tank bioreactors for scalable production of adherent human stem cells. The design addresses a needle‐to‐needle closed process incorporating automated bone marrow collection, cell isolation, expansion, and collection into cryovials for patient delivery. AUTOSTEM, a modular, adaptable, fully closed system ensures no direct operator interaction with biological material; all commands are performed through a graphic interface. Seeding of source material, process monitoring, feeding, sampling, harvesting and cryopreservation are automated within the closed platform, comprising two clean room levels enabling both open and closed processes. A bioprocess based on human MSCs expanded on microcarriers was used for proof of concept. Utilizing equivalent culture parameters, the AUTOSTEM robot‐assisted platform successfully performed cell expansion at the liter scale, generating results comparable to manual production, while maintaining cell quality postprocessing. John Wiley & Sons, Inc. 2022-08-06 /pmc/articles/PMC9472012/ /pubmed/36176619 http://dx.doi.org/10.1002/btm2.10387 Text en © 2022 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
Ochs, Jelena
Hanga, Mariana P.
Shaw, Georgina
Duffy, Niamh
Kulik, Michael
Tissin, Nokilaj
Reibert, Daniel
Biermann, Ferdinand
Moutsatsou, Panagiota
Ratnayake, Shibani
Nienow, Alvin
Koenig, Niels
Schmitt, Robert
Rafiq, Qasim
Hewitt, Christopher J.
Barry, Frank
Murphy, J. Mary
Needle to needle robot‐assisted manufacture of cell therapy products
title Needle to needle robot‐assisted manufacture of cell therapy products
title_full Needle to needle robot‐assisted manufacture of cell therapy products
title_fullStr Needle to needle robot‐assisted manufacture of cell therapy products
title_full_unstemmed Needle to needle robot‐assisted manufacture of cell therapy products
title_short Needle to needle robot‐assisted manufacture of cell therapy products
title_sort needle to needle robot‐assisted manufacture of cell therapy products
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472012/
https://www.ncbi.nlm.nih.gov/pubmed/36176619
http://dx.doi.org/10.1002/btm2.10387
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