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Roles of tumor-associated macrophages in anti-PD-1/PD-L1 immunotherapy for solid cancers
In recent years, tumor immunotherapy has made significant progress. However, tumor immunotherapy, particularly immune checkpoint inhibitors (e.g., PD-1/PD-L1 inhibitors), benefits only a tiny proportion of patients in solid cancers. The tumor microenvironment (TME) acts a significant role in tumor i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029244/ https://www.ncbi.nlm.nih.gov/pubmed/36941614 http://dx.doi.org/10.1186/s12943-023-01725-x |
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author | Zhang, Hao Liu, Lin Liu, Jinbo Dang, Pengyuan Hu, Shengyun Yuan, Weitang Sun, Zhenqiang Liu, Yang Wang, Chengzeng |
author_facet | Zhang, Hao Liu, Lin Liu, Jinbo Dang, Pengyuan Hu, Shengyun Yuan, Weitang Sun, Zhenqiang Liu, Yang Wang, Chengzeng |
author_sort | Zhang, Hao |
collection | PubMed |
description | In recent years, tumor immunotherapy has made significant progress. However, tumor immunotherapy, particularly immune checkpoint inhibitors (e.g., PD-1/PD-L1 inhibitors), benefits only a tiny proportion of patients in solid cancers. The tumor microenvironment (TME) acts a significant role in tumor immunotherapy. Studies reported that tumor-associated macrophages (TAMs), as one of the main components of TME, seriously affected the therapeutic effect of PD-1/PD-L1 inhibitors. In this review, we analyzed TAMs from epigenetic and single-cell perspectives and introduced the role and mechanisms of TAMs in anti-programmed death protein 1(anti-PD-1) therapy. In addition, we summarized combination regimens that enhance the efficacy of tumor PD-1/PD-L1 inhibitors and elaborated on the role of the TAMs in different solid cancers. Eventually, the clinical value of TAMs by influencing the therapeutic effect of tumor PD-1/PD-L1 inhibitors was discussed. These above are beneficial to elucidate poor therapeutic effect of PD-1/PD-L1 inhibitors in solid tumors from the point of view of TAMs and explore the strategies to improve its objective remission rate of solid cancers. |
format | Online Article Text |
id | pubmed-10029244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100292442023-03-22 Roles of tumor-associated macrophages in anti-PD-1/PD-L1 immunotherapy for solid cancers Zhang, Hao Liu, Lin Liu, Jinbo Dang, Pengyuan Hu, Shengyun Yuan, Weitang Sun, Zhenqiang Liu, Yang Wang, Chengzeng Mol Cancer Review In recent years, tumor immunotherapy has made significant progress. However, tumor immunotherapy, particularly immune checkpoint inhibitors (e.g., PD-1/PD-L1 inhibitors), benefits only a tiny proportion of patients in solid cancers. The tumor microenvironment (TME) acts a significant role in tumor immunotherapy. Studies reported that tumor-associated macrophages (TAMs), as one of the main components of TME, seriously affected the therapeutic effect of PD-1/PD-L1 inhibitors. In this review, we analyzed TAMs from epigenetic and single-cell perspectives and introduced the role and mechanisms of TAMs in anti-programmed death protein 1(anti-PD-1) therapy. In addition, we summarized combination regimens that enhance the efficacy of tumor PD-1/PD-L1 inhibitors and elaborated on the role of the TAMs in different solid cancers. Eventually, the clinical value of TAMs by influencing the therapeutic effect of tumor PD-1/PD-L1 inhibitors was discussed. These above are beneficial to elucidate poor therapeutic effect of PD-1/PD-L1 inhibitors in solid tumors from the point of view of TAMs and explore the strategies to improve its objective remission rate of solid cancers. BioMed Central 2023-03-21 /pmc/articles/PMC10029244/ /pubmed/36941614 http://dx.doi.org/10.1186/s12943-023-01725-x 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 Zhang, Hao Liu, Lin Liu, Jinbo Dang, Pengyuan Hu, Shengyun Yuan, Weitang Sun, Zhenqiang Liu, Yang Wang, Chengzeng Roles of tumor-associated macrophages in anti-PD-1/PD-L1 immunotherapy for solid cancers |
title | Roles of tumor-associated macrophages in anti-PD-1/PD-L1 immunotherapy for solid cancers |
title_full | Roles of tumor-associated macrophages in anti-PD-1/PD-L1 immunotherapy for solid cancers |
title_fullStr | Roles of tumor-associated macrophages in anti-PD-1/PD-L1 immunotherapy for solid cancers |
title_full_unstemmed | Roles of tumor-associated macrophages in anti-PD-1/PD-L1 immunotherapy for solid cancers |
title_short | Roles of tumor-associated macrophages in anti-PD-1/PD-L1 immunotherapy for solid cancers |
title_sort | roles of tumor-associated macrophages in anti-pd-1/pd-l1 immunotherapy for solid cancers |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029244/ https://www.ncbi.nlm.nih.gov/pubmed/36941614 http://dx.doi.org/10.1186/s12943-023-01725-x |
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