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Targeting the interleukin-17 immune axis for cancer immunotherapy
The role of IL-17 in cancer remains controversial. Emerging evidence suggests that during early oncogenesis IL-17 supports tumor growth, whereas in established tumors IL-17 production by γδ and Th17 cells potentiates antitumor immunity. Consequently, γδ and Th17 cells are attractive targets for immu...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037254/ https://www.ncbi.nlm.nih.gov/pubmed/31727783 http://dx.doi.org/10.1084/jem.20190456 |
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author | Vitiello, Gerardo A. Miller, George |
author_facet | Vitiello, Gerardo A. Miller, George |
author_sort | Vitiello, Gerardo A. |
collection | PubMed |
description | The role of IL-17 in cancer remains controversial. Emerging evidence suggests that during early oncogenesis IL-17 supports tumor growth, whereas in established tumors IL-17 production by γδ and Th17 cells potentiates antitumor immunity. Consequently, γδ and Th17 cells are attractive targets for immunotherapy in the IL-17 immune axis. To optimize IL-17–based immunotherapy, a deeper understanding of the cytokines dictating IL-17 production and the polarity of γδ and Th17 cells is critical. Here, we delve into the dichotomous roles of IL-17 in cancer and provide insight into the tumor microenvironment conducive for successful IL-17–based γδ and Th17 cell immunotherapy. |
format | Online Article Text |
id | pubmed-7037254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70372542020-11-13 Targeting the interleukin-17 immune axis for cancer immunotherapy Vitiello, Gerardo A. Miller, George J Exp Med Reviews The role of IL-17 in cancer remains controversial. Emerging evidence suggests that during early oncogenesis IL-17 supports tumor growth, whereas in established tumors IL-17 production by γδ and Th17 cells potentiates antitumor immunity. Consequently, γδ and Th17 cells are attractive targets for immunotherapy in the IL-17 immune axis. To optimize IL-17–based immunotherapy, a deeper understanding of the cytokines dictating IL-17 production and the polarity of γδ and Th17 cells is critical. Here, we delve into the dichotomous roles of IL-17 in cancer and provide insight into the tumor microenvironment conducive for successful IL-17–based γδ and Th17 cell immunotherapy. Rockefeller University Press 2020-11-14 /pmc/articles/PMC7037254/ /pubmed/31727783 http://dx.doi.org/10.1084/jem.20190456 Text en © 2019 Vitiello and Miller http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Reviews Vitiello, Gerardo A. Miller, George Targeting the interleukin-17 immune axis for cancer immunotherapy |
title | Targeting the interleukin-17 immune axis for cancer immunotherapy |
title_full | Targeting the interleukin-17 immune axis for cancer immunotherapy |
title_fullStr | Targeting the interleukin-17 immune axis for cancer immunotherapy |
title_full_unstemmed | Targeting the interleukin-17 immune axis for cancer immunotherapy |
title_short | Targeting the interleukin-17 immune axis for cancer immunotherapy |
title_sort | targeting the interleukin-17 immune axis for cancer immunotherapy |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037254/ https://www.ncbi.nlm.nih.gov/pubmed/31727783 http://dx.doi.org/10.1084/jem.20190456 |
work_keys_str_mv | AT vitiellogerardoa targetingtheinterleukin17immuneaxisforcancerimmunotherapy AT millergeorge targetingtheinterleukin17immuneaxisforcancerimmunotherapy |