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Chimeric Antigen Receptor Cell Therapy: Overcoming Obstacles to Battle Cancer

Chimeric antigen receptors (CAR) are fusion proteins engineered from antigen recognition, signaling, and costimulatory domains that can be used to reprogram T cells to specifically target tumor cells expressing specific antigens. Current CAR-T cell technology utilizes the patient’s own T cells to st...

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Detalles Bibliográficos
Autores principales: Petty, Amy J., Heyman, Benjamin, Yang, Yiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226583/
https://www.ncbi.nlm.nih.gov/pubmed/32244520
http://dx.doi.org/10.3390/cancers12040842
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author Petty, Amy J.
Heyman, Benjamin
Yang, Yiping
author_facet Petty, Amy J.
Heyman, Benjamin
Yang, Yiping
author_sort Petty, Amy J.
collection PubMed
description Chimeric antigen receptors (CAR) are fusion proteins engineered from antigen recognition, signaling, and costimulatory domains that can be used to reprogram T cells to specifically target tumor cells expressing specific antigens. Current CAR-T cell technology utilizes the patient’s own T cells to stably express CARs and has achieved exciting clinical success in the past few years. However, current CAR-T cell therapy still faces several challenges, including suboptimal persistence and potency, impaired trafficking to solid tumors, local immunosuppression within the tumor microenvironment and intrinsic toxicity associated with CAR-T cells. This review focuses on recent strategies to improve the clinical efficacy of CAR-T cell therapy and other exciting CAR approaches currently under investigation, including CAR natural killer (NK) and NKT cell therapies.
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spelling pubmed-72265832020-05-18 Chimeric Antigen Receptor Cell Therapy: Overcoming Obstacles to Battle Cancer Petty, Amy J. Heyman, Benjamin Yang, Yiping Cancers (Basel) Review Chimeric antigen receptors (CAR) are fusion proteins engineered from antigen recognition, signaling, and costimulatory domains that can be used to reprogram T cells to specifically target tumor cells expressing specific antigens. Current CAR-T cell technology utilizes the patient’s own T cells to stably express CARs and has achieved exciting clinical success in the past few years. However, current CAR-T cell therapy still faces several challenges, including suboptimal persistence and potency, impaired trafficking to solid tumors, local immunosuppression within the tumor microenvironment and intrinsic toxicity associated with CAR-T cells. This review focuses on recent strategies to improve the clinical efficacy of CAR-T cell therapy and other exciting CAR approaches currently under investigation, including CAR natural killer (NK) and NKT cell therapies. MDPI 2020-03-31 /pmc/articles/PMC7226583/ /pubmed/32244520 http://dx.doi.org/10.3390/cancers12040842 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Petty, Amy J.
Heyman, Benjamin
Yang, Yiping
Chimeric Antigen Receptor Cell Therapy: Overcoming Obstacles to Battle Cancer
title Chimeric Antigen Receptor Cell Therapy: Overcoming Obstacles to Battle Cancer
title_full Chimeric Antigen Receptor Cell Therapy: Overcoming Obstacles to Battle Cancer
title_fullStr Chimeric Antigen Receptor Cell Therapy: Overcoming Obstacles to Battle Cancer
title_full_unstemmed Chimeric Antigen Receptor Cell Therapy: Overcoming Obstacles to Battle Cancer
title_short Chimeric Antigen Receptor Cell Therapy: Overcoming Obstacles to Battle Cancer
title_sort chimeric antigen receptor cell therapy: overcoming obstacles to battle cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226583/
https://www.ncbi.nlm.nih.gov/pubmed/32244520
http://dx.doi.org/10.3390/cancers12040842
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