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Protection against influenza infection requires early recognition by inflammatory dendritic cells through C-type lectin receptor SIGN-R1
The initial phase of influenza infection occurs in the upper respiratory tract and the trachea. Yet, little is known about the initial events whereby the immune system recognises the virus and controls viral dissemination. Here, we report that inflammatory dendritic cells (IDC) are recruited to the...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817362/ https://www.ncbi.nlm.nih.gov/pubmed/31358982 http://dx.doi.org/10.1038/s41564-019-0506-6 |
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author | Palomino-Segura, Miguel Perez, Laurent Farsakoglu, Yagmur Virgilio, Tommaso Latino, Irene D’Antuono, Rocco Chatziandreou, Nikolaos Pizzagalli, Diego U. Wang, Guojun García-Sastre, Adolfo Sallusto, Federica Carroll, Michael C. Neyrolles, Olivier Gonzalez, Santiago F. |
author_facet | Palomino-Segura, Miguel Perez, Laurent Farsakoglu, Yagmur Virgilio, Tommaso Latino, Irene D’Antuono, Rocco Chatziandreou, Nikolaos Pizzagalli, Diego U. Wang, Guojun García-Sastre, Adolfo Sallusto, Federica Carroll, Michael C. Neyrolles, Olivier Gonzalez, Santiago F. |
author_sort | Palomino-Segura, Miguel |
collection | PubMed |
description | The initial phase of influenza infection occurs in the upper respiratory tract and the trachea. Yet, little is known about the initial events whereby the immune system recognises the virus and controls viral dissemination. Here, we report that inflammatory dendritic cells (IDC) are recruited to the trachea early on following influenza infection through type I interferon-mediated production of the chemokine CCL2. We further show that recruited IDC express the C-type lectin receptor SIGN-R1 that mediates direct recognition of the virus by interacting with the N-linked glycans present in the glycoproteins of the virion envelope. Activation of IDC via SIGN-R1 triggers the production of the chemokines CCL5, CXCL9 and CXCL10 that initiate the recruitment of protective natural killer (NK) cells in the infected trachea. In the absence of SIGN-R1, the recruitment and activation of NK cells is impaired, which leads to uncontrolled viral proliferation. Altogether, our results shed light on the orchestration of the early cellular and molecular events involved in the immune protection against influenza. |
format | Online Article Text |
id | pubmed-6817362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-68173622020-01-29 Protection against influenza infection requires early recognition by inflammatory dendritic cells through C-type lectin receptor SIGN-R1 Palomino-Segura, Miguel Perez, Laurent Farsakoglu, Yagmur Virgilio, Tommaso Latino, Irene D’Antuono, Rocco Chatziandreou, Nikolaos Pizzagalli, Diego U. Wang, Guojun García-Sastre, Adolfo Sallusto, Federica Carroll, Michael C. Neyrolles, Olivier Gonzalez, Santiago F. Nat Microbiol Article The initial phase of influenza infection occurs in the upper respiratory tract and the trachea. Yet, little is known about the initial events whereby the immune system recognises the virus and controls viral dissemination. Here, we report that inflammatory dendritic cells (IDC) are recruited to the trachea early on following influenza infection through type I interferon-mediated production of the chemokine CCL2. We further show that recruited IDC express the C-type lectin receptor SIGN-R1 that mediates direct recognition of the virus by interacting with the N-linked glycans present in the glycoproteins of the virion envelope. Activation of IDC via SIGN-R1 triggers the production of the chemokines CCL5, CXCL9 and CXCL10 that initiate the recruitment of protective natural killer (NK) cells in the infected trachea. In the absence of SIGN-R1, the recruitment and activation of NK cells is impaired, which leads to uncontrolled viral proliferation. Altogether, our results shed light on the orchestration of the early cellular and molecular events involved in the immune protection against influenza. 2019-06-12 2019-07-29 /pmc/articles/PMC6817362/ /pubmed/31358982 http://dx.doi.org/10.1038/s41564-019-0506-6 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Palomino-Segura, Miguel Perez, Laurent Farsakoglu, Yagmur Virgilio, Tommaso Latino, Irene D’Antuono, Rocco Chatziandreou, Nikolaos Pizzagalli, Diego U. Wang, Guojun García-Sastre, Adolfo Sallusto, Federica Carroll, Michael C. Neyrolles, Olivier Gonzalez, Santiago F. Protection against influenza infection requires early recognition by inflammatory dendritic cells through C-type lectin receptor SIGN-R1 |
title | Protection against influenza infection requires early recognition by inflammatory dendritic cells through C-type lectin receptor SIGN-R1 |
title_full | Protection against influenza infection requires early recognition by inflammatory dendritic cells through C-type lectin receptor SIGN-R1 |
title_fullStr | Protection against influenza infection requires early recognition by inflammatory dendritic cells through C-type lectin receptor SIGN-R1 |
title_full_unstemmed | Protection against influenza infection requires early recognition by inflammatory dendritic cells through C-type lectin receptor SIGN-R1 |
title_short | Protection against influenza infection requires early recognition by inflammatory dendritic cells through C-type lectin receptor SIGN-R1 |
title_sort | protection against influenza infection requires early recognition by inflammatory dendritic cells through c-type lectin receptor sign-r1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817362/ https://www.ncbi.nlm.nih.gov/pubmed/31358982 http://dx.doi.org/10.1038/s41564-019-0506-6 |
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