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CAR T Cells: Cancer Cell Surface Receptors Are the Target for Cancer Therapy

Immunotherapy has become a prominent strategy for the treatment of cancer. A method that improves the immune system’s ability to attack a tumor (Enhances antigen binding). Targeted killing of malignant cells by adoptive transfer of chimeric antigen receptor (CAR) T cells is a promising immunotherapy...

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Detalles Bibliográficos
Autores principales: Shademan, Behrouz, Karamad, Vahidreza, Nourazarian, Alireza, Avcı, Cigir Biray
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9348524/
https://www.ncbi.nlm.nih.gov/pubmed/35935042
http://dx.doi.org/10.34172/apb.2022.051
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author Shademan, Behrouz
Karamad, Vahidreza
Nourazarian, Alireza
Avcı, Cigir Biray
author_facet Shademan, Behrouz
Karamad, Vahidreza
Nourazarian, Alireza
Avcı, Cigir Biray
author_sort Shademan, Behrouz
collection PubMed
description Immunotherapy has become a prominent strategy for the treatment of cancer. A method that improves the immune system’s ability to attack a tumor (Enhances antigen binding). Targeted killing of malignant cells by adoptive transfer of chimeric antigen receptor (CAR) T cells is a promising immunotherapy technique in the treatment of cancers. For this purpose, the patient’s immune cells, with genetic engineering aid, are loaded with chimeric receptors that have particular antigen binding and activate cytotoxic T lymphocytes. That increases the effectiveness of immune cells and destroying cancer cells. This review discusses the basic structure and function of CAR-T cells and how antigenic targets are identified to treat different cancers and address the disadvantages of this treatment for cancer.
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spelling pubmed-93485242022-08-06 CAR T Cells: Cancer Cell Surface Receptors Are the Target for Cancer Therapy Shademan, Behrouz Karamad, Vahidreza Nourazarian, Alireza Avcı, Cigir Biray Adv Pharm Bull Review Article Immunotherapy has become a prominent strategy for the treatment of cancer. A method that improves the immune system’s ability to attack a tumor (Enhances antigen binding). Targeted killing of malignant cells by adoptive transfer of chimeric antigen receptor (CAR) T cells is a promising immunotherapy technique in the treatment of cancers. For this purpose, the patient’s immune cells, with genetic engineering aid, are loaded with chimeric receptors that have particular antigen binding and activate cytotoxic T lymphocytes. That increases the effectiveness of immune cells and destroying cancer cells. This review discusses the basic structure and function of CAR-T cells and how antigenic targets are identified to treat different cancers and address the disadvantages of this treatment for cancer. Tabriz University of Medical Sciences 2022-05 2021-08-22 /pmc/articles/PMC9348524/ /pubmed/35935042 http://dx.doi.org/10.34172/apb.2022.051 Text en ©2022 The Authors. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, as long as the original authors and source are cited. No permission is required from the authors or the publishers.
spellingShingle Review Article
Shademan, Behrouz
Karamad, Vahidreza
Nourazarian, Alireza
Avcı, Cigir Biray
CAR T Cells: Cancer Cell Surface Receptors Are the Target for Cancer Therapy
title CAR T Cells: Cancer Cell Surface Receptors Are the Target for Cancer Therapy
title_full CAR T Cells: Cancer Cell Surface Receptors Are the Target for Cancer Therapy
title_fullStr CAR T Cells: Cancer Cell Surface Receptors Are the Target for Cancer Therapy
title_full_unstemmed CAR T Cells: Cancer Cell Surface Receptors Are the Target for Cancer Therapy
title_short CAR T Cells: Cancer Cell Surface Receptors Are the Target for Cancer Therapy
title_sort car t cells: cancer cell surface receptors are the target for cancer therapy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9348524/
https://www.ncbi.nlm.nih.gov/pubmed/35935042
http://dx.doi.org/10.34172/apb.2022.051
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