Armored CAR T-Cells: The Next Chapter in T-Cell Cancer Immunotherapy

Elizabeth R Hawkins, Reena R D’Souza, Astero Klampatsa Division of Cancer Therapeutics, The Institute of Cancer Research, London, UKCorrespondence: Astero KlampatsaThoracic Oncology Immunotherapy Group, Division of Cancer Therapeutics, The Institute of Cancer Research, 15 Cotswold Road, Su...

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Autores principales: Hawkins ER, D'Souza RR, Klampatsa A
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Publicado: Dove Medical Press 2021
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spelling oai:doaj.org-article:ebb64adc425b40b8aba3cb8d1d89150f2021-12-02T14:39:09ZArmored CAR T-Cells: The Next Chapter in T-Cell Cancer Immunotherapy1177-5491https://doaj.org/article/ebb64adc425b40b8aba3cb8d1d89150f2021-04-01T00:00:00Zhttps://www.dovepress.com/armored-car-t-cells-the-next-chapter-in-t-cell-cancer-immunotherapy-peer-reviewed-article-BTThttps://doaj.org/toc/1177-5491Elizabeth R Hawkins, Reena R D’Souza, Astero Klampatsa Division of Cancer Therapeutics, The Institute of Cancer Research, London, UKCorrespondence: Astero KlampatsaThoracic Oncology Immunotherapy Group, Division of Cancer Therapeutics, The Institute of Cancer Research, 15 Cotswold Road, Sutton, London, SM2 5NG, UKTel +44 208 722 4090Email astero.klampatsa@icr.ac.ukAbstract: Chimeric antigen receptor (CAR) T-cell therapy engineers T-cells to express a synthetic receptor which redirects effector function to the tumor, to improve efficacy and reduce toxicities associated with conventional treatments, such as radiotherapy and chemotherapy. This approach has proved effective in treating hematological malignancies; however, the same effects have not been observed in solid tumors. The immunosuppressive tumor microenvironment (TME) creates a significant barrier to solid tumor efficacy and reduces the anti-cancer activity of endogenous tumor-resident immune cells, enabling cancer progression. In recent years, researchers have attempted to enhance CAR T-cell function in the TME by engineering the cells to express various proteins alongside the CAR. Examples of this engineering include inducing CAR T-cells to secrete cytokines or express cytokine receptors to modulate the cytokine milieu of the TME. Alternatively, the CAR T-cell may secrete antibody-like proteins to target a range of tumor antigens. Collectively, these methods are termed armored CAR T-cell therapy, and in this review, we will discuss the range of armored CAR T-cell approaches which have been investigated to date.Keywords: armored CAR T-cells, immunotherapy, tumor microenvironment, solid tumors, immunosuppression, cell therapyHawkins ERD'Souza RRKlampatsa ADove Medical Pressarticlearmored car t-cellsimmunotherapytumor microenvironmentsolid tumorsimmunosuppressioncell therapyMedicine (General)R5-920ENBiologics: Targets & Therapy, Vol Volume 15, Pp 95-105 (2021)
institution DOAJ
collection DOAJ
language EN
topic armored car t-cells
immunotherapy
tumor microenvironment
solid tumors
immunosuppression
cell therapy
Medicine (General)
R5-920
spellingShingle armored car t-cells
immunotherapy
tumor microenvironment
solid tumors
immunosuppression
cell therapy
Medicine (General)
R5-920
Hawkins ER
D'Souza RR
Klampatsa A
Armored CAR T-Cells: The Next Chapter in T-Cell Cancer Immunotherapy
description Elizabeth R Hawkins, Reena R D’Souza, Astero Klampatsa Division of Cancer Therapeutics, The Institute of Cancer Research, London, UKCorrespondence: Astero KlampatsaThoracic Oncology Immunotherapy Group, Division of Cancer Therapeutics, The Institute of Cancer Research, 15 Cotswold Road, Sutton, London, SM2 5NG, UKTel +44 208 722 4090Email astero.klampatsa@icr.ac.ukAbstract: Chimeric antigen receptor (CAR) T-cell therapy engineers T-cells to express a synthetic receptor which redirects effector function to the tumor, to improve efficacy and reduce toxicities associated with conventional treatments, such as radiotherapy and chemotherapy. This approach has proved effective in treating hematological malignancies; however, the same effects have not been observed in solid tumors. The immunosuppressive tumor microenvironment (TME) creates a significant barrier to solid tumor efficacy and reduces the anti-cancer activity of endogenous tumor-resident immune cells, enabling cancer progression. In recent years, researchers have attempted to enhance CAR T-cell function in the TME by engineering the cells to express various proteins alongside the CAR. Examples of this engineering include inducing CAR T-cells to secrete cytokines or express cytokine receptors to modulate the cytokine milieu of the TME. Alternatively, the CAR T-cell may secrete antibody-like proteins to target a range of tumor antigens. Collectively, these methods are termed armored CAR T-cell therapy, and in this review, we will discuss the range of armored CAR T-cell approaches which have been investigated to date.Keywords: armored CAR T-cells, immunotherapy, tumor microenvironment, solid tumors, immunosuppression, cell therapy
format article
author Hawkins ER
D'Souza RR
Klampatsa A
author_facet Hawkins ER
D'Souza RR
Klampatsa A
author_sort Hawkins ER
title Armored CAR T-Cells: The Next Chapter in T-Cell Cancer Immunotherapy
title_short Armored CAR T-Cells: The Next Chapter in T-Cell Cancer Immunotherapy
title_full Armored CAR T-Cells: The Next Chapter in T-Cell Cancer Immunotherapy
title_fullStr Armored CAR T-Cells: The Next Chapter in T-Cell Cancer Immunotherapy
title_full_unstemmed Armored CAR T-Cells: The Next Chapter in T-Cell Cancer Immunotherapy
title_sort armored car t-cells: the next chapter in t-cell cancer immunotherapy
publisher Dove Medical Press
publishDate 2021
url https://doaj.org/article/ebb64adc425b40b8aba3cb8d1d89150f
work_keys_str_mv AT hawkinser armoredcartcellsthenextchapterintcellcancerimmunotherapy
AT dsouzarr armoredcartcellsthenextchapterintcellcancerimmunotherapy
AT klampatsaa armoredcartcellsthenextchapterintcellcancerimmunotherapy
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