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Targeting 4-1BB for tumor immunotherapy from bench to bedside
Immune dysfunction has been proposed as a factor that may contribute to disease progression. Emerging evidence suggests that immunotherapy aims to abolish cancer progression by modulating the balance of the tumor microenvironment. 4-1BB (also known as CD137 and TNFRS9), a member of tumor necrosis fa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523430/ https://www.ncbi.nlm.nih.gov/pubmed/36189243 http://dx.doi.org/10.3389/fimmu.2022.975926 |
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author | Wang, Ya-Tao Ji, Wei-Dong Jiao, Hong-Mei Lu, Ang Chen, Kun-Feng Liu, Qi-Bing |
author_facet | Wang, Ya-Tao Ji, Wei-Dong Jiao, Hong-Mei Lu, Ang Chen, Kun-Feng Liu, Qi-Bing |
author_sort | Wang, Ya-Tao |
collection | PubMed |
description | Immune dysfunction has been proposed as a factor that may contribute to disease progression. Emerging evidence suggests that immunotherapy aims to abolish cancer progression by modulating the balance of the tumor microenvironment. 4-1BB (also known as CD137 and TNFRS9), a member of tumor necrosis factor receptor superfamily, has been validated as an extremely attractive and promising target for immunotherapy due to the upregulated expression in the tumor environment and its involvement in tumor progression. More importantly, 4-1BB-based immunotherapy approaches have manifested powerful antitumor effects in clinical trials targeting 4-1BB alone or in combination with other immune checkpoints. In this review, we will summarize the structure and expression of 4-1BB and its ligand, discuss the role of 4-1BB in the microenvironment and tumor progression, and update the development of drugs targeting 4-1BB. The purpose of the review is to furnish a comprehensive overview of the potential of 4-1BB as an immunotherapeutic target and to discuss recent advances and prospects for 4-1BB in cancer therapy. |
format | Online Article Text |
id | pubmed-9523430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95234302022-10-01 Targeting 4-1BB for tumor immunotherapy from bench to bedside Wang, Ya-Tao Ji, Wei-Dong Jiao, Hong-Mei Lu, Ang Chen, Kun-Feng Liu, Qi-Bing Front Immunol Immunology Immune dysfunction has been proposed as a factor that may contribute to disease progression. Emerging evidence suggests that immunotherapy aims to abolish cancer progression by modulating the balance of the tumor microenvironment. 4-1BB (also known as CD137 and TNFRS9), a member of tumor necrosis factor receptor superfamily, has been validated as an extremely attractive and promising target for immunotherapy due to the upregulated expression in the tumor environment and its involvement in tumor progression. More importantly, 4-1BB-based immunotherapy approaches have manifested powerful antitumor effects in clinical trials targeting 4-1BB alone or in combination with other immune checkpoints. In this review, we will summarize the structure and expression of 4-1BB and its ligand, discuss the role of 4-1BB in the microenvironment and tumor progression, and update the development of drugs targeting 4-1BB. The purpose of the review is to furnish a comprehensive overview of the potential of 4-1BB as an immunotherapeutic target and to discuss recent advances and prospects for 4-1BB in cancer therapy. Frontiers Media S.A. 2022-09-16 /pmc/articles/PMC9523430/ /pubmed/36189243 http://dx.doi.org/10.3389/fimmu.2022.975926 Text en Copyright © 2022 Wang, Ji, Jiao, Lu, Chen and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Wang, Ya-Tao Ji, Wei-Dong Jiao, Hong-Mei Lu, Ang Chen, Kun-Feng Liu, Qi-Bing Targeting 4-1BB for tumor immunotherapy from bench to bedside |
title | Targeting 4-1BB for tumor immunotherapy from bench to bedside |
title_full | Targeting 4-1BB for tumor immunotherapy from bench to bedside |
title_fullStr | Targeting 4-1BB for tumor immunotherapy from bench to bedside |
title_full_unstemmed | Targeting 4-1BB for tumor immunotherapy from bench to bedside |
title_short | Targeting 4-1BB for tumor immunotherapy from bench to bedside |
title_sort | targeting 4-1bb for tumor immunotherapy from bench to bedside |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523430/ https://www.ncbi.nlm.nih.gov/pubmed/36189243 http://dx.doi.org/10.3389/fimmu.2022.975926 |
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