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Enhanced Anti-lymphoma Activity of CAR19-iNKT Cells Underpinned by Dual CD19 and CD1d Targeting
Chimeric antigen receptor anti-CD19 (CAR19)-T cell immunotherapy-induced clinical remissions in CD19(+) B cell lymphomas are often short lived. We tested whether CAR19-engineering of the CD1d-restricted invariant natural killer T (iNKT) cells would result in enhanced anti-lymphoma activity. CAR19-iN...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179961/ https://www.ncbi.nlm.nih.gov/pubmed/30300581 http://dx.doi.org/10.1016/j.ccell.2018.08.017 |
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author | Rotolo, Antonia Caputo, Valentina S. Holubova, Monika Baxan, Nicoleta Dubois, Olivier Chaudhry, Mohammed Suhail Xiao, Xiaolin Goudevenou, Katerina Pitcher, David S. Petevi, Kyriaki Kachramanoglou, Carolina Iles, Sandra Naresh, Kikkeri Maher, John Karadimitris, Anastasios |
author_facet | Rotolo, Antonia Caputo, Valentina S. Holubova, Monika Baxan, Nicoleta Dubois, Olivier Chaudhry, Mohammed Suhail Xiao, Xiaolin Goudevenou, Katerina Pitcher, David S. Petevi, Kyriaki Kachramanoglou, Carolina Iles, Sandra Naresh, Kikkeri Maher, John Karadimitris, Anastasios |
author_sort | Rotolo, Antonia |
collection | PubMed |
description | Chimeric antigen receptor anti-CD19 (CAR19)-T cell immunotherapy-induced clinical remissions in CD19(+) B cell lymphomas are often short lived. We tested whether CAR19-engineering of the CD1d-restricted invariant natural killer T (iNKT) cells would result in enhanced anti-lymphoma activity. CAR19-iNKT cells co-operatively activated by CD1d- and CAR19-CD19-dependent interactions are more effective than CAR19-T cells against CD1d-expressing lymphomas in vitro and in vivo. The swifter in vivo anti-lymphoma activity of CAR19-iNKT cells and their enhanced ability to eradicate brain lymphomas underpinned an improved tumor-free and overall survival. CD1D transcriptional de-repression by all-trans retinoic acid results in further enhanced cytotoxicity of CAR19-iNKT cells against CD19(+) chronic lymphocytic leukemia cells. Thus, iNKT cells are a highly efficient platform for CAR-based immunotherapy of lymphomas and possibly other CD1d-expressing cancers. |
format | Online Article Text |
id | pubmed-6179961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61799612018-10-12 Enhanced Anti-lymphoma Activity of CAR19-iNKT Cells Underpinned by Dual CD19 and CD1d Targeting Rotolo, Antonia Caputo, Valentina S. Holubova, Monika Baxan, Nicoleta Dubois, Olivier Chaudhry, Mohammed Suhail Xiao, Xiaolin Goudevenou, Katerina Pitcher, David S. Petevi, Kyriaki Kachramanoglou, Carolina Iles, Sandra Naresh, Kikkeri Maher, John Karadimitris, Anastasios Cancer Cell Article Chimeric antigen receptor anti-CD19 (CAR19)-T cell immunotherapy-induced clinical remissions in CD19(+) B cell lymphomas are often short lived. We tested whether CAR19-engineering of the CD1d-restricted invariant natural killer T (iNKT) cells would result in enhanced anti-lymphoma activity. CAR19-iNKT cells co-operatively activated by CD1d- and CAR19-CD19-dependent interactions are more effective than CAR19-T cells against CD1d-expressing lymphomas in vitro and in vivo. The swifter in vivo anti-lymphoma activity of CAR19-iNKT cells and their enhanced ability to eradicate brain lymphomas underpinned an improved tumor-free and overall survival. CD1D transcriptional de-repression by all-trans retinoic acid results in further enhanced cytotoxicity of CAR19-iNKT cells against CD19(+) chronic lymphocytic leukemia cells. Thus, iNKT cells are a highly efficient platform for CAR-based immunotherapy of lymphomas and possibly other CD1d-expressing cancers. Cell Press 2018-10-08 /pmc/articles/PMC6179961/ /pubmed/30300581 http://dx.doi.org/10.1016/j.ccell.2018.08.017 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Rotolo, Antonia Caputo, Valentina S. Holubova, Monika Baxan, Nicoleta Dubois, Olivier Chaudhry, Mohammed Suhail Xiao, Xiaolin Goudevenou, Katerina Pitcher, David S. Petevi, Kyriaki Kachramanoglou, Carolina Iles, Sandra Naresh, Kikkeri Maher, John Karadimitris, Anastasios Enhanced Anti-lymphoma Activity of CAR19-iNKT Cells Underpinned by Dual CD19 and CD1d Targeting |
title | Enhanced Anti-lymphoma Activity of CAR19-iNKT Cells Underpinned by Dual CD19 and CD1d Targeting |
title_full | Enhanced Anti-lymphoma Activity of CAR19-iNKT Cells Underpinned by Dual CD19 and CD1d Targeting |
title_fullStr | Enhanced Anti-lymphoma Activity of CAR19-iNKT Cells Underpinned by Dual CD19 and CD1d Targeting |
title_full_unstemmed | Enhanced Anti-lymphoma Activity of CAR19-iNKT Cells Underpinned by Dual CD19 and CD1d Targeting |
title_short | Enhanced Anti-lymphoma Activity of CAR19-iNKT Cells Underpinned by Dual CD19 and CD1d Targeting |
title_sort | enhanced anti-lymphoma activity of car19-inkt cells underpinned by dual cd19 and cd1d targeting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179961/ https://www.ncbi.nlm.nih.gov/pubmed/30300581 http://dx.doi.org/10.1016/j.ccell.2018.08.017 |
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