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Type I Interferons and Natural Killer Cell Regulation in Cancer
Type I interferons (IFNs) are known to mediate antitumor effects against several tumor types and have therefore been commonly used in clinical anticancer treatment. However, how IFN signaling exerts its beneficial effects is only partially understood. The clinically relevant activity of type I IFNs...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374157/ https://www.ncbi.nlm.nih.gov/pubmed/28408907 http://dx.doi.org/10.3389/fimmu.2017.00304 |
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author | Müller, Lena Aigner, Petra Stoiber, Dagmar |
author_facet | Müller, Lena Aigner, Petra Stoiber, Dagmar |
author_sort | Müller, Lena |
collection | PubMed |
description | Type I interferons (IFNs) are known to mediate antitumor effects against several tumor types and have therefore been commonly used in clinical anticancer treatment. However, how IFN signaling exerts its beneficial effects is only partially understood. The clinically relevant activity of type I IFNs has been mainly attributed to their role in tumor immune surveillance. Different mechanisms have been postulated to explain how type I IFNs stimulate the immune system. On the one hand, they modulate innate immune cell subsets such as natural killer (NK) cells. On the other hand, type I IFNs also influence adaptive immune responses. Here, we review evidence for the impact of type I IFNs on immune surveillance against cancer and highlight the role of NK cells therein. |
format | Online Article Text |
id | pubmed-5374157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53741572017-04-13 Type I Interferons and Natural Killer Cell Regulation in Cancer Müller, Lena Aigner, Petra Stoiber, Dagmar Front Immunol Immunology Type I interferons (IFNs) are known to mediate antitumor effects against several tumor types and have therefore been commonly used in clinical anticancer treatment. However, how IFN signaling exerts its beneficial effects is only partially understood. The clinically relevant activity of type I IFNs has been mainly attributed to their role in tumor immune surveillance. Different mechanisms have been postulated to explain how type I IFNs stimulate the immune system. On the one hand, they modulate innate immune cell subsets such as natural killer (NK) cells. On the other hand, type I IFNs also influence adaptive immune responses. Here, we review evidence for the impact of type I IFNs on immune surveillance against cancer and highlight the role of NK cells therein. Frontiers Media S.A. 2017-03-31 /pmc/articles/PMC5374157/ /pubmed/28408907 http://dx.doi.org/10.3389/fimmu.2017.00304 Text en Copyright © 2017 Müller, Aigner and Stoiber. http://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) or licensor 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 Müller, Lena Aigner, Petra Stoiber, Dagmar Type I Interferons and Natural Killer Cell Regulation in Cancer |
title | Type I Interferons and Natural Killer Cell Regulation in Cancer |
title_full | Type I Interferons and Natural Killer Cell Regulation in Cancer |
title_fullStr | Type I Interferons and Natural Killer Cell Regulation in Cancer |
title_full_unstemmed | Type I Interferons and Natural Killer Cell Regulation in Cancer |
title_short | Type I Interferons and Natural Killer Cell Regulation in Cancer |
title_sort | type i interferons and natural killer cell regulation in cancer |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374157/ https://www.ncbi.nlm.nih.gov/pubmed/28408907 http://dx.doi.org/10.3389/fimmu.2017.00304 |
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