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Chimeric Antigen Receptor T Cell Therapy: A Novel Modality for Immune Modulation

Cancer remains a leading cause of death, despite multimodal treatment approaches. Even in patients with a healthy immune response, cancer cells can escape the immune system during tumorigenesis. Cancer cells incapacitate the normal cell-mediated immune system by expressing immune modulation ligands...

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Detalles Bibliográficos
Autores principales: Yoon, Somy, Eom, Gwang Hyeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chonnam National University Medical School 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976774/
https://www.ncbi.nlm.nih.gov/pubmed/32021836
http://dx.doi.org/10.4068/cmj.2020.56.1.6
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author Yoon, Somy
Eom, Gwang Hyeon
author_facet Yoon, Somy
Eom, Gwang Hyeon
author_sort Yoon, Somy
collection PubMed
description Cancer remains a leading cause of death, despite multimodal treatment approaches. Even in patients with a healthy immune response, cancer cells can escape the immune system during tumorigenesis. Cancer cells incapacitate the normal cell-mediated immune system by expressing immune modulation ligands such as programmed death (PD) ligand 1, the B7 molecule, or secreting activators of immune modulators. Chimeric antigen receptor (CAR) T cells were originally designed to target cancer cells. Engineered approaches allow CAR T cells, which possess a simplified yet specific receptor, to be easily activated in limited situations. CAR T cell treatment is a derivative of the antigen-antibody reaction and can be applied to various diseases. In this review, the current successes of CAR T cells in cancer treatment and the therapeutic potential of CAR T cells are discussed.
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spelling pubmed-69767742020-02-04 Chimeric Antigen Receptor T Cell Therapy: A Novel Modality for Immune Modulation Yoon, Somy Eom, Gwang Hyeon Chonnam Med J Review Article Cancer remains a leading cause of death, despite multimodal treatment approaches. Even in patients with a healthy immune response, cancer cells can escape the immune system during tumorigenesis. Cancer cells incapacitate the normal cell-mediated immune system by expressing immune modulation ligands such as programmed death (PD) ligand 1, the B7 molecule, or secreting activators of immune modulators. Chimeric antigen receptor (CAR) T cells were originally designed to target cancer cells. Engineered approaches allow CAR T cells, which possess a simplified yet specific receptor, to be easily activated in limited situations. CAR T cell treatment is a derivative of the antigen-antibody reaction and can be applied to various diseases. In this review, the current successes of CAR T cells in cancer treatment and the therapeutic potential of CAR T cells are discussed. Chonnam National University Medical School 2020-01 2020-01-22 /pmc/articles/PMC6976774/ /pubmed/32021836 http://dx.doi.org/10.4068/cmj.2020.56.1.6 Text en © Chonnam Medical Journal, 2020 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Yoon, Somy
Eom, Gwang Hyeon
Chimeric Antigen Receptor T Cell Therapy: A Novel Modality for Immune Modulation
title Chimeric Antigen Receptor T Cell Therapy: A Novel Modality for Immune Modulation
title_full Chimeric Antigen Receptor T Cell Therapy: A Novel Modality for Immune Modulation
title_fullStr Chimeric Antigen Receptor T Cell Therapy: A Novel Modality for Immune Modulation
title_full_unstemmed Chimeric Antigen Receptor T Cell Therapy: A Novel Modality for Immune Modulation
title_short Chimeric Antigen Receptor T Cell Therapy: A Novel Modality for Immune Modulation
title_sort chimeric antigen receptor t cell therapy: a novel modality for immune modulation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976774/
https://www.ncbi.nlm.nih.gov/pubmed/32021836
http://dx.doi.org/10.4068/cmj.2020.56.1.6
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