Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Wei, Jordan, Kimberly R, Schulte, Brian, Purev, Enkhtsetseg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
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
_version_ 1783362335286493184
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
work_keys_str_mv AT zhangwei characterizationofclinicalgradecd19chimericantigenreceptortcellsproducedusingautomatedclinimacsprodigysystem
AT jordankimberlyr characterizationofclinicalgradecd19chimericantigenreceptortcellsproducedusingautomatedclinimacsprodigysystem
AT schultebrian characterizationofclinicalgradecd19chimericantigenreceptortcellsproducedusingautomatedclinimacsprodigysystem
AT purevenkhtsetseg characterizationofclinicalgradecd19chimericantigenreceptortcellsproducedusingautomatedclinimacsprodigysystem