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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7226583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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