Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Stock, Sophia, Kluever, Anna-Kristina, Endres, Stefan, Kobold, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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
_version_ 1784656563356565504
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
work_keys_str_mv AT stocksophia enhancedchimericantigenreceptortcelltherapythroughcoapplicationofsynergisticcombinationpartners
AT klueverannakristina enhancedchimericantigenreceptortcelltherapythroughcoapplicationofsynergisticcombinationpartners
AT endresstefan enhancedchimericantigenreceptortcelltherapythroughcoapplicationofsynergisticcombinationpartners
AT koboldsebastian enhancedchimericantigenreceptortcelltherapythroughcoapplicationofsynergisticcombinationpartners