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Interplay between myeloid-derived suppressor cells (MDSCs) and Th17 cells: foe or friend?
Myeloid-derived suppressor cells (MDSCs) and Th17 cells were first discovered in the fields of cancer and autoimmunity, respectively. In recent years, their activities have been explored in other biological and pathological conditions, such as infective diseases and solid organ transplantation. Howe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5085246/ https://www.ncbi.nlm.nih.gov/pubmed/27007054 http://dx.doi.org/10.18632/oncotarget.8204 |
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author | Wen, Liang Gong, Ping Liang, Chao Shou, Dawei Liu, Baoqing Chen, Yiwen Bao, Changqian Chen, Li Liu, Xiaowei Liang, Tingbo Gong, Weihua |
author_facet | Wen, Liang Gong, Ping Liang, Chao Shou, Dawei Liu, Baoqing Chen, Yiwen Bao, Changqian Chen, Li Liu, Xiaowei Liang, Tingbo Gong, Weihua |
author_sort | Wen, Liang |
collection | PubMed |
description | Myeloid-derived suppressor cells (MDSCs) and Th17 cells were first discovered in the fields of cancer and autoimmunity, respectively. In recent years, their activities have been explored in other biological and pathological conditions, such as infective diseases and solid organ transplantation. However, the interplay between MDSCs and Th17 cells and the mechanism of their interaction remain obscure. This review summarized and analyzed the relationship between MDSCs and Th17 cells, both of which participate in tumor, autoimmune disease, infection and other conditions. In tumors, the increase in MDSCs at the tumor site is usually accompanied by the accumulation of Th17 cells. However, their relationship is inconsistent in different tumors. In arthritic mice or rheumatoid arthritis (RA) patients, an increase in MDSCs, which could ameliorate disease symptoms, causes decreased IL-17A gene expression and Th17 cells accumulation. Furthermore, we concluded that the interaction between MDSCs and Th17 cells is mainly mediated by cytokines. However, the mechanisms require further investigation. Determining the details of their interplay will provide a better understanding of immune networks and could lead to the development of immunotherapeutic strategies in the future. |
format | Online Article Text |
id | pubmed-5085246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50852462016-10-31 Interplay between myeloid-derived suppressor cells (MDSCs) and Th17 cells: foe or friend? Wen, Liang Gong, Ping Liang, Chao Shou, Dawei Liu, Baoqing Chen, Yiwen Bao, Changqian Chen, Li Liu, Xiaowei Liang, Tingbo Gong, Weihua Oncotarget Review Myeloid-derived suppressor cells (MDSCs) and Th17 cells were first discovered in the fields of cancer and autoimmunity, respectively. In recent years, their activities have been explored in other biological and pathological conditions, such as infective diseases and solid organ transplantation. However, the interplay between MDSCs and Th17 cells and the mechanism of their interaction remain obscure. This review summarized and analyzed the relationship between MDSCs and Th17 cells, both of which participate in tumor, autoimmune disease, infection and other conditions. In tumors, the increase in MDSCs at the tumor site is usually accompanied by the accumulation of Th17 cells. However, their relationship is inconsistent in different tumors. In arthritic mice or rheumatoid arthritis (RA) patients, an increase in MDSCs, which could ameliorate disease symptoms, causes decreased IL-17A gene expression and Th17 cells accumulation. Furthermore, we concluded that the interaction between MDSCs and Th17 cells is mainly mediated by cytokines. However, the mechanisms require further investigation. Determining the details of their interplay will provide a better understanding of immune networks and could lead to the development of immunotherapeutic strategies in the future. Impact Journals LLC 2016-03-19 /pmc/articles/PMC5085246/ /pubmed/27007054 http://dx.doi.org/10.18632/oncotarget.8204 Text en Copyright: © 2016 Wen et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Wen, Liang Gong, Ping Liang, Chao Shou, Dawei Liu, Baoqing Chen, Yiwen Bao, Changqian Chen, Li Liu, Xiaowei Liang, Tingbo Gong, Weihua Interplay between myeloid-derived suppressor cells (MDSCs) and Th17 cells: foe or friend? |
title | Interplay between myeloid-derived suppressor cells (MDSCs) and Th17 cells: foe or friend? |
title_full | Interplay between myeloid-derived suppressor cells (MDSCs) and Th17 cells: foe or friend? |
title_fullStr | Interplay between myeloid-derived suppressor cells (MDSCs) and Th17 cells: foe or friend? |
title_full_unstemmed | Interplay between myeloid-derived suppressor cells (MDSCs) and Th17 cells: foe or friend? |
title_short | Interplay between myeloid-derived suppressor cells (MDSCs) and Th17 cells: foe or friend? |
title_sort | interplay between myeloid-derived suppressor cells (mdscs) and th17 cells: foe or friend? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5085246/ https://www.ncbi.nlm.nih.gov/pubmed/27007054 http://dx.doi.org/10.18632/oncotarget.8204 |
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