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Investigating chimeric antigen receptor T cell therapy and the potential for cancer immunotherapy (Review)

Immunotherapy has emerged as a crucial treatment option, particularly for types of cancer that display resistance to conventional therapies. A remarkable breakthrough in this field is the development of chimeric antigen receptor (CAR) T cell therapy. CAR T cells are generated by engineering the T ce...

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Autores principales: Poojary, Rayansh, Song, Andy Fang, Song, Benny Shone, Song, Carly Shaw, Wang, Liqing, Song, Jianxun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619195/
https://www.ncbi.nlm.nih.gov/pubmed/37920415
http://dx.doi.org/10.3892/mco.2023.2691
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author Poojary, Rayansh
Song, Andy Fang
Song, Benny Shone
Song, Carly Shaw
Wang, Liqing
Song, Jianxun
author_facet Poojary, Rayansh
Song, Andy Fang
Song, Benny Shone
Song, Carly Shaw
Wang, Liqing
Song, Jianxun
author_sort Poojary, Rayansh
collection PubMed
description Immunotherapy has emerged as a crucial treatment option, particularly for types of cancer that display resistance to conventional therapies. A remarkable breakthrough in this field is the development of chimeric antigen receptor (CAR) T cell therapy. CAR T cells are generated by engineering the T cells of a patient to express receptors that can recognize specific tumor antigens. This groundbreaking approach has demonstrated impressive outcomes in hematologic malignancies, including diffuse large B cell lymphoma, B cell acute lymphoblastic leukemia and multiple myeloma. Despite these significant successes, CAR T cell therapy has encountered challenges in its application against solid tumors, leading to limited success in these cases. Consequently, researchers are actively exploring novel strategies to enhance the efficacy of CAR T cells. The focus lies on augmenting CAR T cell trafficking to tumors while preventing the development of CAR T cell exhaustion and dysfunction. The present review aimed to provide a comprehensive analysis of the achievements and limitations of CAR T cell therapy in the context of cancer treatment. By understanding both the successes and hurdles, further advancements in this promising area of research can be developed. Overall, immunotherapy, particularly CAR T cell therapy, has opened up novel possibilities for cancer treatment, offering hope to patients with previously untreatable malignancies. However, to fully realize its potential, ongoing research and innovative strategies are essential in overcoming the challenges posed by solid tumors and maximizing CAR T cell efficacy in clinical settings.
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spelling pubmed-106191952023-11-02 Investigating chimeric antigen receptor T cell therapy and the potential for cancer immunotherapy (Review) Poojary, Rayansh Song, Andy Fang Song, Benny Shone Song, Carly Shaw Wang, Liqing Song, Jianxun Mol Clin Oncol Review Immunotherapy has emerged as a crucial treatment option, particularly for types of cancer that display resistance to conventional therapies. A remarkable breakthrough in this field is the development of chimeric antigen receptor (CAR) T cell therapy. CAR T cells are generated by engineering the T cells of a patient to express receptors that can recognize specific tumor antigens. This groundbreaking approach has demonstrated impressive outcomes in hematologic malignancies, including diffuse large B cell lymphoma, B cell acute lymphoblastic leukemia and multiple myeloma. Despite these significant successes, CAR T cell therapy has encountered challenges in its application against solid tumors, leading to limited success in these cases. Consequently, researchers are actively exploring novel strategies to enhance the efficacy of CAR T cells. The focus lies on augmenting CAR T cell trafficking to tumors while preventing the development of CAR T cell exhaustion and dysfunction. The present review aimed to provide a comprehensive analysis of the achievements and limitations of CAR T cell therapy in the context of cancer treatment. By understanding both the successes and hurdles, further advancements in this promising area of research can be developed. Overall, immunotherapy, particularly CAR T cell therapy, has opened up novel possibilities for cancer treatment, offering hope to patients with previously untreatable malignancies. However, to fully realize its potential, ongoing research and innovative strategies are essential in overcoming the challenges posed by solid tumors and maximizing CAR T cell efficacy in clinical settings. D.A. Spandidos 2023-10-12 /pmc/articles/PMC10619195/ /pubmed/37920415 http://dx.doi.org/10.3892/mco.2023.2691 Text en Copyright: © Poojary et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Poojary, Rayansh
Song, Andy Fang
Song, Benny Shone
Song, Carly Shaw
Wang, Liqing
Song, Jianxun
Investigating chimeric antigen receptor T cell therapy and the potential for cancer immunotherapy (Review)
title Investigating chimeric antigen receptor T cell therapy and the potential for cancer immunotherapy (Review)
title_full Investigating chimeric antigen receptor T cell therapy and the potential for cancer immunotherapy (Review)
title_fullStr Investigating chimeric antigen receptor T cell therapy and the potential for cancer immunotherapy (Review)
title_full_unstemmed Investigating chimeric antigen receptor T cell therapy and the potential for cancer immunotherapy (Review)
title_short Investigating chimeric antigen receptor T cell therapy and the potential for cancer immunotherapy (Review)
title_sort investigating chimeric antigen receptor t cell therapy and the potential for cancer immunotherapy (review)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619195/
https://www.ncbi.nlm.nih.gov/pubmed/37920415
http://dx.doi.org/10.3892/mco.2023.2691
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