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Cancer Immunotherapies Targeting Tumor-Associated Regulatory T Cells

Tumor-associated regulatory T cells (Tregs) are important effectors in the tumor microenvironment (TME), acting as accomplices in the promotion of tumor progression. Currently, the importance of removing the immunosuppressive activity in the TME has received its due attention, and Tregs have been fo...

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Detalles Bibliográficos
Autores principales: Ge, Xiaoxu, Zhao, Yamei, Chen, Chao, Wang, Jian, Sun, Lifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917600/
https://www.ncbi.nlm.nih.gov/pubmed/31997881
http://dx.doi.org/10.2147/OTT.S231052
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author Ge, Xiaoxu
Zhao, Yamei
Chen, Chao
Wang, Jian
Sun, Lifeng
author_facet Ge, Xiaoxu
Zhao, Yamei
Chen, Chao
Wang, Jian
Sun, Lifeng
author_sort Ge, Xiaoxu
collection PubMed
description Tumor-associated regulatory T cells (Tregs) are important effectors in the tumor microenvironment (TME), acting as accomplices in the promotion of tumor progression. Currently, the importance of removing the immunosuppressive activity in the TME has received its due attention, and Tregs have been focused on. The cytokine-receptor axes are among the essential signaling pathways in immunocytes, and tumor-associated Tregs are no exception. Therefore, manipulating cytokine-receptor pathways may be a promising effective strategy for treating various malignancies. Here, we summarize the classification, immunosuppressive mechanisms, existing immunotherapies, and potential biomarkers related to tumor-infiltrating Tregs to guide the development of effective cancer immunotherapies.
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spelling pubmed-69176002020-01-29 Cancer Immunotherapies Targeting Tumor-Associated Regulatory T Cells Ge, Xiaoxu Zhao, Yamei Chen, Chao Wang, Jian Sun, Lifeng Onco Targets Ther Review Tumor-associated regulatory T cells (Tregs) are important effectors in the tumor microenvironment (TME), acting as accomplices in the promotion of tumor progression. Currently, the importance of removing the immunosuppressive activity in the TME has received its due attention, and Tregs have been focused on. The cytokine-receptor axes are among the essential signaling pathways in immunocytes, and tumor-associated Tregs are no exception. Therefore, manipulating cytokine-receptor pathways may be a promising effective strategy for treating various malignancies. Here, we summarize the classification, immunosuppressive mechanisms, existing immunotherapies, and potential biomarkers related to tumor-infiltrating Tregs to guide the development of effective cancer immunotherapies. Dove 2019-12-13 /pmc/articles/PMC6917600/ /pubmed/31997881 http://dx.doi.org/10.2147/OTT.S231052 Text en © 2019 Ge et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Ge, Xiaoxu
Zhao, Yamei
Chen, Chao
Wang, Jian
Sun, Lifeng
Cancer Immunotherapies Targeting Tumor-Associated Regulatory T Cells
title Cancer Immunotherapies Targeting Tumor-Associated Regulatory T Cells
title_full Cancer Immunotherapies Targeting Tumor-Associated Regulatory T Cells
title_fullStr Cancer Immunotherapies Targeting Tumor-Associated Regulatory T Cells
title_full_unstemmed Cancer Immunotherapies Targeting Tumor-Associated Regulatory T Cells
title_short Cancer Immunotherapies Targeting Tumor-Associated Regulatory T Cells
title_sort cancer immunotherapies targeting tumor-associated regulatory t cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917600/
https://www.ncbi.nlm.nih.gov/pubmed/31997881
http://dx.doi.org/10.2147/OTT.S231052
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