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Utility and Drawbacks of Chimeric Antigen Receptor T Cell (CAR-T) Therapy in Lung Cancer
The present treatments for lung cancer include surgical resection, radiation, chemotherapy, targeted therapy, and immunotherapy. Despite advances in therapies, the prognosis of lung cancer has not been substantially improved in recent years. Chimeric antigen receptor (CAR)-T cell immunotherapy has a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201083/ https://www.ncbi.nlm.nih.gov/pubmed/35720364 http://dx.doi.org/10.3389/fimmu.2022.903562 |
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author | Kandra, Prameela Nandigama, Rajender Eul, Bastian Huber, Magdalena Kobold, Sebastian Seeger, Werner Grimminger, Friedrich Savai, Rajkumar |
author_facet | Kandra, Prameela Nandigama, Rajender Eul, Bastian Huber, Magdalena Kobold, Sebastian Seeger, Werner Grimminger, Friedrich Savai, Rajkumar |
author_sort | Kandra, Prameela |
collection | PubMed |
description | The present treatments for lung cancer include surgical resection, radiation, chemotherapy, targeted therapy, and immunotherapy. Despite advances in therapies, the prognosis of lung cancer has not been substantially improved in recent years. Chimeric antigen receptor (CAR)-T cell immunotherapy has attracted growing interest in the treatment of various malignancies. Despite CAR-T cell therapy emerging as a novel potential therapeutic option with promising results in refractory and relapsed leukemia, many challenges limit its therapeutic efficacy in solid tumors including lung cancer. In this landscape, studies have identified several obstacles to the effective use of CAR-T cell therapy including antigen heterogeneity, the immunosuppressive tumor microenvironment, and tumor penetration by CAR-T cells. Here, we review CAR-T cell design; present the results of CAR-T cell therapies in preclinical and clinical studies in lung cancer; describe existing challenges and toxicities; and discuss strategies to improve therapeutic efficacy of CAR-T cells. |
format | Online Article Text |
id | pubmed-9201083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92010832022-06-17 Utility and Drawbacks of Chimeric Antigen Receptor T Cell (CAR-T) Therapy in Lung Cancer Kandra, Prameela Nandigama, Rajender Eul, Bastian Huber, Magdalena Kobold, Sebastian Seeger, Werner Grimminger, Friedrich Savai, Rajkumar Front Immunol Immunology The present treatments for lung cancer include surgical resection, radiation, chemotherapy, targeted therapy, and immunotherapy. Despite advances in therapies, the prognosis of lung cancer has not been substantially improved in recent years. Chimeric antigen receptor (CAR)-T cell immunotherapy has attracted growing interest in the treatment of various malignancies. Despite CAR-T cell therapy emerging as a novel potential therapeutic option with promising results in refractory and relapsed leukemia, many challenges limit its therapeutic efficacy in solid tumors including lung cancer. In this landscape, studies have identified several obstacles to the effective use of CAR-T cell therapy including antigen heterogeneity, the immunosuppressive tumor microenvironment, and tumor penetration by CAR-T cells. Here, we review CAR-T cell design; present the results of CAR-T cell therapies in preclinical and clinical studies in lung cancer; describe existing challenges and toxicities; and discuss strategies to improve therapeutic efficacy of CAR-T cells. Frontiers Media S.A. 2022-06-02 /pmc/articles/PMC9201083/ /pubmed/35720364 http://dx.doi.org/10.3389/fimmu.2022.903562 Text en Copyright © 2022 Kandra, Nandigama, Eul, Huber, Kobold, Seeger, Grimminger and Savai https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Kandra, Prameela Nandigama, Rajender Eul, Bastian Huber, Magdalena Kobold, Sebastian Seeger, Werner Grimminger, Friedrich Savai, Rajkumar Utility and Drawbacks of Chimeric Antigen Receptor T Cell (CAR-T) Therapy in Lung Cancer |
title | Utility and Drawbacks of Chimeric Antigen Receptor T Cell (CAR-T) Therapy in Lung Cancer |
title_full | Utility and Drawbacks of Chimeric Antigen Receptor T Cell (CAR-T) Therapy in Lung Cancer |
title_fullStr | Utility and Drawbacks of Chimeric Antigen Receptor T Cell (CAR-T) Therapy in Lung Cancer |
title_full_unstemmed | Utility and Drawbacks of Chimeric Antigen Receptor T Cell (CAR-T) Therapy in Lung Cancer |
title_short | Utility and Drawbacks of Chimeric Antigen Receptor T Cell (CAR-T) Therapy in Lung Cancer |
title_sort | utility and drawbacks of chimeric antigen receptor t cell (car-t) therapy in lung cancer |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201083/ https://www.ncbi.nlm.nih.gov/pubmed/35720364 http://dx.doi.org/10.3389/fimmu.2022.903562 |
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