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Gamma delta T-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment

As a nontraditional T-cell subgroup, γδT cells have gained popularity in the field of immunotherapy in recent years. They have extraordinary antitumor potential and prospects for clinical application. Immune checkpoint inhibitors (ICIs), which are efficacious in tumor patients, have become pioneer d...

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Autores principales: Gao, Zhifei, Bai, Yifeng, Lin, Anqi, Jiang, Aimin, Zhou, Chaozheng, Cheng, Quan, Liu, Zaoqu, Chen, Xin, Zhang, Jian, Luo, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930367/
https://www.ncbi.nlm.nih.gov/pubmed/36793048
http://dx.doi.org/10.1186/s12943-023-01722-0
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author Gao, Zhifei
Bai, Yifeng
Lin, Anqi
Jiang, Aimin
Zhou, Chaozheng
Cheng, Quan
Liu, Zaoqu
Chen, Xin
Zhang, Jian
Luo, Peng
author_facet Gao, Zhifei
Bai, Yifeng
Lin, Anqi
Jiang, Aimin
Zhou, Chaozheng
Cheng, Quan
Liu, Zaoqu
Chen, Xin
Zhang, Jian
Luo, Peng
author_sort Gao, Zhifei
collection PubMed
description As a nontraditional T-cell subgroup, γδT cells have gained popularity in the field of immunotherapy in recent years. They have extraordinary antitumor potential and prospects for clinical application. Immune checkpoint inhibitors (ICIs), which are efficacious in tumor patients, have become pioneer drugs in the field of tumor immunotherapy since they were incorporated into clinical practice. In addition, γδT cells that have infiltrated into tumor tissues are found to be in a state of exhaustion or anergy, and there is upregulation of many immune checkpoints (ICs) on their surface, suggesting that γδT cells have a similar ability to respond to ICIs as traditional effector T cells. Studies have shown that targeting ICs can reverse the dysfunctional state of γδT cells in the tumor microenvironment (TME) and exert antitumor effects by improving γδT-cell proliferation and activation and enhancing cytotoxicity. Clarification of the functional state of γδT cells in the TME and the mechanisms underlying their interaction with ICs will solidify ICIs combined with γδT cells as a good treatment option. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12943-023-01722-0.
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spelling pubmed-99303672023-02-16 Gamma delta T-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment Gao, Zhifei Bai, Yifeng Lin, Anqi Jiang, Aimin Zhou, Chaozheng Cheng, Quan Liu, Zaoqu Chen, Xin Zhang, Jian Luo, Peng Mol Cancer Review As a nontraditional T-cell subgroup, γδT cells have gained popularity in the field of immunotherapy in recent years. They have extraordinary antitumor potential and prospects for clinical application. Immune checkpoint inhibitors (ICIs), which are efficacious in tumor patients, have become pioneer drugs in the field of tumor immunotherapy since they were incorporated into clinical practice. In addition, γδT cells that have infiltrated into tumor tissues are found to be in a state of exhaustion or anergy, and there is upregulation of many immune checkpoints (ICs) on their surface, suggesting that γδT cells have a similar ability to respond to ICIs as traditional effector T cells. Studies have shown that targeting ICs can reverse the dysfunctional state of γδT cells in the tumor microenvironment (TME) and exert antitumor effects by improving γδT-cell proliferation and activation and enhancing cytotoxicity. Clarification of the functional state of γδT cells in the TME and the mechanisms underlying their interaction with ICs will solidify ICIs combined with γδT cells as a good treatment option. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12943-023-01722-0. BioMed Central 2023-02-15 /pmc/articles/PMC9930367/ /pubmed/36793048 http://dx.doi.org/10.1186/s12943-023-01722-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Gao, Zhifei
Bai, Yifeng
Lin, Anqi
Jiang, Aimin
Zhou, Chaozheng
Cheng, Quan
Liu, Zaoqu
Chen, Xin
Zhang, Jian
Luo, Peng
Gamma delta T-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment
title Gamma delta T-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment
title_full Gamma delta T-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment
title_fullStr Gamma delta T-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment
title_full_unstemmed Gamma delta T-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment
title_short Gamma delta T-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment
title_sort gamma delta t-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930367/
https://www.ncbi.nlm.nih.gov/pubmed/36793048
http://dx.doi.org/10.1186/s12943-023-01722-0
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