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IL-27 signaling activates skin cells to induce innate antiviral proteins and protects against Zika virus infection
In the skin, antiviral proteins and other immune molecules serve as the first line of innate antiviral defense. Here, we identify and characterize the induction of cutaneous innate antiviral proteins in response to IL-27 and its functional role during cutaneous defense against Zika virus infection....
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112749/ https://www.ncbi.nlm.nih.gov/pubmed/32270034 http://dx.doi.org/10.1126/sciadv.aay3245 |
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author | Kwock, Jeffery T. Handfield, Chelsea Suwanpradid, Jutamas Hoang, Peter McFadden, Michael J. Labagnara, Kevin F. Floyd, Lauren Shannon, Jessica Uppala, Ranjitha Sarkar, Mrinal K. Gudjonsson, Johann E. Corcoran, David L. Lazear, Helen M. Sempowski, Gregory Horner, Stacy M. MacLeod, Amanda S. |
author_facet | Kwock, Jeffery T. Handfield, Chelsea Suwanpradid, Jutamas Hoang, Peter McFadden, Michael J. Labagnara, Kevin F. Floyd, Lauren Shannon, Jessica Uppala, Ranjitha Sarkar, Mrinal K. Gudjonsson, Johann E. Corcoran, David L. Lazear, Helen M. Sempowski, Gregory Horner, Stacy M. MacLeod, Amanda S. |
author_sort | Kwock, Jeffery T. |
collection | PubMed |
description | In the skin, antiviral proteins and other immune molecules serve as the first line of innate antiviral defense. Here, we identify and characterize the induction of cutaneous innate antiviral proteins in response to IL-27 and its functional role during cutaneous defense against Zika virus infection. Transcriptional and phenotypic profiling of epidermal keratinocytes treated with IL-27 demonstrated activation of antiviral proteins OAS1, OAS2, OASL, and MX1 in the skin of both mice and humans. IL-27–mediated antiviral protein induction was found to occur in a STAT1- and IRF3-dependent but STAT2-independent manner. Moreover, using IL27ra mice, we demonstrate a significant role for IL-27 in inhibiting Zika virus morbidity and mortality following cutaneous, but not intravenous, inoculation. Together, our results demonstrate a critical and previously unrecognized role for IL-27 in cutaneous innate antiviral immunity against Zika virus. |
format | Online Article Text |
id | pubmed-7112749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71127492020-04-08 IL-27 signaling activates skin cells to induce innate antiviral proteins and protects against Zika virus infection Kwock, Jeffery T. Handfield, Chelsea Suwanpradid, Jutamas Hoang, Peter McFadden, Michael J. Labagnara, Kevin F. Floyd, Lauren Shannon, Jessica Uppala, Ranjitha Sarkar, Mrinal K. Gudjonsson, Johann E. Corcoran, David L. Lazear, Helen M. Sempowski, Gregory Horner, Stacy M. MacLeod, Amanda S. Sci Adv Research Articles In the skin, antiviral proteins and other immune molecules serve as the first line of innate antiviral defense. Here, we identify and characterize the induction of cutaneous innate antiviral proteins in response to IL-27 and its functional role during cutaneous defense against Zika virus infection. Transcriptional and phenotypic profiling of epidermal keratinocytes treated with IL-27 demonstrated activation of antiviral proteins OAS1, OAS2, OASL, and MX1 in the skin of both mice and humans. IL-27–mediated antiviral protein induction was found to occur in a STAT1- and IRF3-dependent but STAT2-independent manner. Moreover, using IL27ra mice, we demonstrate a significant role for IL-27 in inhibiting Zika virus morbidity and mortality following cutaneous, but not intravenous, inoculation. Together, our results demonstrate a critical and previously unrecognized role for IL-27 in cutaneous innate antiviral immunity against Zika virus. American Association for the Advancement of Science 2020-04-01 /pmc/articles/PMC7112749/ /pubmed/32270034 http://dx.doi.org/10.1126/sciadv.aay3245 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Kwock, Jeffery T. Handfield, Chelsea Suwanpradid, Jutamas Hoang, Peter McFadden, Michael J. Labagnara, Kevin F. Floyd, Lauren Shannon, Jessica Uppala, Ranjitha Sarkar, Mrinal K. Gudjonsson, Johann E. Corcoran, David L. Lazear, Helen M. Sempowski, Gregory Horner, Stacy M. MacLeod, Amanda S. IL-27 signaling activates skin cells to induce innate antiviral proteins and protects against Zika virus infection |
title | IL-27 signaling activates skin cells to induce innate antiviral proteins and protects against Zika virus infection |
title_full | IL-27 signaling activates skin cells to induce innate antiviral proteins and protects against Zika virus infection |
title_fullStr | IL-27 signaling activates skin cells to induce innate antiviral proteins and protects against Zika virus infection |
title_full_unstemmed | IL-27 signaling activates skin cells to induce innate antiviral proteins and protects against Zika virus infection |
title_short | IL-27 signaling activates skin cells to induce innate antiviral proteins and protects against Zika virus infection |
title_sort | il-27 signaling activates skin cells to induce innate antiviral proteins and protects against zika virus infection |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112749/ https://www.ncbi.nlm.nih.gov/pubmed/32270034 http://dx.doi.org/10.1126/sciadv.aay3245 |
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