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Characterization of clinical grade CD19 chimeric antigen receptor T cells produced using automated CliniMACS Prodigy system
BACKGROUND: Chimeric antigen receptor (CAR) T-cell therapy is highly effective for treating acute lymphoblastic leukemia and non-Hodgkin’s lymphoma with high rate complete responses. However, the broad clinical application of CAR T-cell therapy has been challenging, largely due to the lack of widesp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181073/ https://www.ncbi.nlm.nih.gov/pubmed/30323566 http://dx.doi.org/10.2147/DDDT.S175113 |
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author | Zhang, Wei Jordan, Kimberly R Schulte, Brian Purev, Enkhtsetseg |
author_facet | Zhang, Wei Jordan, Kimberly R Schulte, Brian Purev, Enkhtsetseg |
author_sort | Zhang, Wei |
collection | PubMed |
description | BACKGROUND: Chimeric antigen receptor (CAR) T-cell therapy is highly effective for treating acute lymphoblastic leukemia and non-Hodgkin’s lymphoma with high rate complete responses. However, the broad clinical application of CAR T-cell therapy has been challenging, largely due to the lack of widespread ability to produce and high cost of CAR T-cell products using traditional methods of production. Automated cell processing in a closed system has emerged as a potential method to increase the feasibility of producing CAR T cells locally at academic centers due to its minimal reliance on experienced labor, thereby making the process less expensive and more consistent than traditional methods of production. METHOD: In this study, we describe the successful production of clinical grade CD19 CAR T cells using the Miltenyi CliniMACS Prodigy Automated Cell Processor at University of Colorado Anschutz Medical Campus in a rapid manner with a high frequent CD19 CAR expression. RESULTS: The final CAR T-cell product is highly active, low in immune suppression, and absent in exhaustion. Full panel cytokine assays also showed elevated production of Th1 cytokines upon IL-2 stimulation when specifically killing CD19+ target cells. CONCLUSION: These results demonstrate the feasibility of producing CAR T cells locally in a university hospital setting using automated cell processor for future clinical applications. |
format | Online Article Text |
id | pubmed-6181073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61810732018-10-15 Characterization of clinical grade CD19 chimeric antigen receptor T cells produced using automated CliniMACS Prodigy system Zhang, Wei Jordan, Kimberly R Schulte, Brian Purev, Enkhtsetseg Drug Des Devel Ther Original Research BACKGROUND: Chimeric antigen receptor (CAR) T-cell therapy is highly effective for treating acute lymphoblastic leukemia and non-Hodgkin’s lymphoma with high rate complete responses. However, the broad clinical application of CAR T-cell therapy has been challenging, largely due to the lack of widespread ability to produce and high cost of CAR T-cell products using traditional methods of production. Automated cell processing in a closed system has emerged as a potential method to increase the feasibility of producing CAR T cells locally at academic centers due to its minimal reliance on experienced labor, thereby making the process less expensive and more consistent than traditional methods of production. METHOD: In this study, we describe the successful production of clinical grade CD19 CAR T cells using the Miltenyi CliniMACS Prodigy Automated Cell Processor at University of Colorado Anschutz Medical Campus in a rapid manner with a high frequent CD19 CAR expression. RESULTS: The final CAR T-cell product is highly active, low in immune suppression, and absent in exhaustion. Full panel cytokine assays also showed elevated production of Th1 cytokines upon IL-2 stimulation when specifically killing CD19+ target cells. CONCLUSION: These results demonstrate the feasibility of producing CAR T cells locally in a university hospital setting using automated cell processor for future clinical applications. Dove Medical Press 2018-10-05 /pmc/articles/PMC6181073/ /pubmed/30323566 http://dx.doi.org/10.2147/DDDT.S175113 Text en © 2018 Zhang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Zhang, Wei Jordan, Kimberly R Schulte, Brian Purev, Enkhtsetseg Characterization of clinical grade CD19 chimeric antigen receptor T cells produced using automated CliniMACS Prodigy system |
title | Characterization of clinical grade CD19 chimeric antigen receptor T cells produced using automated CliniMACS Prodigy system |
title_full | Characterization of clinical grade CD19 chimeric antigen receptor T cells produced using automated CliniMACS Prodigy system |
title_fullStr | Characterization of clinical grade CD19 chimeric antigen receptor T cells produced using automated CliniMACS Prodigy system |
title_full_unstemmed | Characterization of clinical grade CD19 chimeric antigen receptor T cells produced using automated CliniMACS Prodigy system |
title_short | Characterization of clinical grade CD19 chimeric antigen receptor T cells produced using automated CliniMACS Prodigy system |
title_sort | characterization of clinical grade cd19 chimeric antigen receptor t cells produced using automated clinimacs prodigy system |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181073/ https://www.ncbi.nlm.nih.gov/pubmed/30323566 http://dx.doi.org/10.2147/DDDT.S175113 |
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