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Enhanced Chimeric Antigen Receptor T Cell Therapy through Co-Application of Synergistic Combination Partners
Chimeric antigen receptor (CAR) T cell therapy has achieved remarkable response rates and revolutionized the treatment of patients suffering from defined hematological malignancies. However, many patients still do not respond to this therapy or relapse after an initial remission, underscoring the ne...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869718/ https://www.ncbi.nlm.nih.gov/pubmed/35203517 http://dx.doi.org/10.3390/biomedicines10020307 |
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author | Stock, Sophia Kluever, Anna-Kristina Endres, Stefan Kobold, Sebastian |
author_facet | Stock, Sophia Kluever, Anna-Kristina Endres, Stefan Kobold, Sebastian |
author_sort | Stock, Sophia |
collection | PubMed |
description | Chimeric antigen receptor (CAR) T cell therapy has achieved remarkable response rates and revolutionized the treatment of patients suffering from defined hematological malignancies. However, many patients still do not respond to this therapy or relapse after an initial remission, underscoring the need for improved efficacy. Insufficient in vivo activity, persistence, trafficking, and tumor infiltration of CAR T cells, as well as antigen escape and treatment-associated adverse events, limit the therapeutic success. Multiple strategies and approaches have been investigated to further improve CAR T cell therapy. Besides genetic modification of the CAR itself, the combination with other treatment modalities has the potential to improve this approach. In particular, combining CAR T cells with clinically approved compounds such as monoclonal antibodies and small molecule inhibitors might be a promising strategy. Combination partners could already be applied during the production process to influence the cellular composition and immunophenotype of the final CAR T cell product. Alternatively, simultaneous administration of clinically approved compounds with CAR T cells would be another feasible avenue. In this review, we will discuss current strategies to combine CAR T cells with compounds to overcome recent limitations and further enhance this promising cancer therapy, potentially broadening its application beyond hematology. |
format | Online Article Text |
id | pubmed-8869718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88697182022-02-25 Enhanced Chimeric Antigen Receptor T Cell Therapy through Co-Application of Synergistic Combination Partners Stock, Sophia Kluever, Anna-Kristina Endres, Stefan Kobold, Sebastian Biomedicines Review Chimeric antigen receptor (CAR) T cell therapy has achieved remarkable response rates and revolutionized the treatment of patients suffering from defined hematological malignancies. However, many patients still do not respond to this therapy or relapse after an initial remission, underscoring the need for improved efficacy. Insufficient in vivo activity, persistence, trafficking, and tumor infiltration of CAR T cells, as well as antigen escape and treatment-associated adverse events, limit the therapeutic success. Multiple strategies and approaches have been investigated to further improve CAR T cell therapy. Besides genetic modification of the CAR itself, the combination with other treatment modalities has the potential to improve this approach. In particular, combining CAR T cells with clinically approved compounds such as monoclonal antibodies and small molecule inhibitors might be a promising strategy. Combination partners could already be applied during the production process to influence the cellular composition and immunophenotype of the final CAR T cell product. Alternatively, simultaneous administration of clinically approved compounds with CAR T cells would be another feasible avenue. In this review, we will discuss current strategies to combine CAR T cells with compounds to overcome recent limitations and further enhance this promising cancer therapy, potentially broadening its application beyond hematology. MDPI 2022-01-28 /pmc/articles/PMC8869718/ /pubmed/35203517 http://dx.doi.org/10.3390/biomedicines10020307 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Stock, Sophia Kluever, Anna-Kristina Endres, Stefan Kobold, Sebastian Enhanced Chimeric Antigen Receptor T Cell Therapy through Co-Application of Synergistic Combination Partners |
title | Enhanced Chimeric Antigen Receptor T Cell Therapy through Co-Application of Synergistic Combination Partners |
title_full | Enhanced Chimeric Antigen Receptor T Cell Therapy through Co-Application of Synergistic Combination Partners |
title_fullStr | Enhanced Chimeric Antigen Receptor T Cell Therapy through Co-Application of Synergistic Combination Partners |
title_full_unstemmed | Enhanced Chimeric Antigen Receptor T Cell Therapy through Co-Application of Synergistic Combination Partners |
title_short | Enhanced Chimeric Antigen Receptor T Cell Therapy through Co-Application of Synergistic Combination Partners |
title_sort | enhanced chimeric antigen receptor t cell therapy through co-application of synergistic combination partners |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869718/ https://www.ncbi.nlm.nih.gov/pubmed/35203517 http://dx.doi.org/10.3390/biomedicines10020307 |
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