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The biomarkers related to immune related adverse events caused by immune checkpoint inhibitors
The enthusiasm for immune checkpoint inhibitors (ICIs), an efficient tumor treatment model different from traditional treatment, is based on their unprecedented antitumor effect, but the occurrence of immune-related adverse events (irAEs) is an obstacle to the prospect of ICI treatment. IrAEs are a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734811/ https://www.ncbi.nlm.nih.gov/pubmed/33317597 http://dx.doi.org/10.1186/s13046-020-01749-x |
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author | Jia, Xiao-Hui Geng, Lu-Ying Jiang, Pan-Pan Xu, Hong Nan, Ke-Jun Yao, Yu Jiang, Li-Li Sun, Hong Qin, Tian-Jie Guo, Hui |
author_facet | Jia, Xiao-Hui Geng, Lu-Ying Jiang, Pan-Pan Xu, Hong Nan, Ke-Jun Yao, Yu Jiang, Li-Li Sun, Hong Qin, Tian-Jie Guo, Hui |
author_sort | Jia, Xiao-Hui |
collection | PubMed |
description | The enthusiasm for immune checkpoint inhibitors (ICIs), an efficient tumor treatment model different from traditional treatment, is based on their unprecedented antitumor effect, but the occurrence of immune-related adverse events (irAEs) is an obstacle to the prospect of ICI treatment. IrAEs are a discrete toxicity caused by the nonspecific activation of the immune system and can affect almost all tissues and organs. Currently, research on biomarkers mainly focuses on the gastrointestinal tract, endocrine system, skin and lung. Several potential hypotheses concentrate on the overactivation of the immune system, excessive release of inflammatory cytokines, elevated levels of pre-existing autoantibodies, and presence of common antigens between tumors and normal tissues. This review lists the current biomarkers that might predict irAEs and their possible mechanisms for both nonspecific and organ-specific biomarkers. However, the prediction of irAEs remains a major clinical challenge to screen and identify patients who are susceptible to irAEs and likely to benefit from ICIs. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at 10.1186/s13046-020-01749-x. |
format | Online Article Text |
id | pubmed-7734811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77348112020-12-15 The biomarkers related to immune related adverse events caused by immune checkpoint inhibitors Jia, Xiao-Hui Geng, Lu-Ying Jiang, Pan-Pan Xu, Hong Nan, Ke-Jun Yao, Yu Jiang, Li-Li Sun, Hong Qin, Tian-Jie Guo, Hui J Exp Clin Cancer Res Review The enthusiasm for immune checkpoint inhibitors (ICIs), an efficient tumor treatment model different from traditional treatment, is based on their unprecedented antitumor effect, but the occurrence of immune-related adverse events (irAEs) is an obstacle to the prospect of ICI treatment. IrAEs are a discrete toxicity caused by the nonspecific activation of the immune system and can affect almost all tissues and organs. Currently, research on biomarkers mainly focuses on the gastrointestinal tract, endocrine system, skin and lung. Several potential hypotheses concentrate on the overactivation of the immune system, excessive release of inflammatory cytokines, elevated levels of pre-existing autoantibodies, and presence of common antigens between tumors and normal tissues. This review lists the current biomarkers that might predict irAEs and their possible mechanisms for both nonspecific and organ-specific biomarkers. However, the prediction of irAEs remains a major clinical challenge to screen and identify patients who are susceptible to irAEs and likely to benefit from ICIs. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at 10.1186/s13046-020-01749-x. BioMed Central 2020-12-14 /pmc/articles/PMC7734811/ /pubmed/33317597 http://dx.doi.org/10.1186/s13046-020-01749-x Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Jia, Xiao-Hui Geng, Lu-Ying Jiang, Pan-Pan Xu, Hong Nan, Ke-Jun Yao, Yu Jiang, Li-Li Sun, Hong Qin, Tian-Jie Guo, Hui The biomarkers related to immune related adverse events caused by immune checkpoint inhibitors |
title | The biomarkers related to immune related adverse events caused by immune checkpoint inhibitors |
title_full | The biomarkers related to immune related adverse events caused by immune checkpoint inhibitors |
title_fullStr | The biomarkers related to immune related adverse events caused by immune checkpoint inhibitors |
title_full_unstemmed | The biomarkers related to immune related adverse events caused by immune checkpoint inhibitors |
title_short | The biomarkers related to immune related adverse events caused by immune checkpoint inhibitors |
title_sort | biomarkers related to immune related adverse events caused by immune checkpoint inhibitors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734811/ https://www.ncbi.nlm.nih.gov/pubmed/33317597 http://dx.doi.org/10.1186/s13046-020-01749-x |
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