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Vicious circle: systemic autoreactivity in Ro52/TRIM21-deficient mice
Dysregulated innate responses, particularly excessive activation of interferon (IFN) pathways, have been implicated in the development of autoimmune pathologies. Autoreactivity frequently targets IFN-inducible genes such as the Ro autoantigens, which ubiquitinate and inhibit interferon regulatory fa...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722177/ https://www.ncbi.nlm.nih.gov/pubmed/19635865 http://dx.doi.org/10.1084/jem.20091507 |
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author | Bolland, Silvia Garcia-Sastre, Adolfo |
author_facet | Bolland, Silvia Garcia-Sastre, Adolfo |
author_sort | Bolland, Silvia |
collection | PubMed |
description | Dysregulated innate responses, particularly excessive activation of interferon (IFN) pathways, have been implicated in the development of autoimmune pathologies. Autoreactivity frequently targets IFN-inducible genes such as the Ro autoantigens, which ubiquitinate and inhibit interferon regulatory factors (IRFs). A new study validates the role of these common autoantigens in preventing autoimmunity. The findings reveal that injury-induced systemic autoimmune disease is exacerbated in the absence of Ro52/Trim21 and is driven by the IL-23–Th17 pathway. |
format | Text |
id | pubmed-2722177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27221772010-02-03 Vicious circle: systemic autoreactivity in Ro52/TRIM21-deficient mice Bolland, Silvia Garcia-Sastre, Adolfo J Exp Med Commentary Dysregulated innate responses, particularly excessive activation of interferon (IFN) pathways, have been implicated in the development of autoimmune pathologies. Autoreactivity frequently targets IFN-inducible genes such as the Ro autoantigens, which ubiquitinate and inhibit interferon regulatory factors (IRFs). A new study validates the role of these common autoantigens in preventing autoimmunity. The findings reveal that injury-induced systemic autoimmune disease is exacerbated in the absence of Ro52/Trim21 and is driven by the IL-23–Th17 pathway. The Rockefeller University Press 2009-08-03 /pmc/articles/PMC2722177/ /pubmed/19635865 http://dx.doi.org/10.1084/jem.20091507 Text en © 2009 The Rockefeller University Press 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.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Commentary Bolland, Silvia Garcia-Sastre, Adolfo Vicious circle: systemic autoreactivity in Ro52/TRIM21-deficient mice |
title | Vicious circle: systemic autoreactivity in Ro52/TRIM21-deficient mice |
title_full | Vicious circle: systemic autoreactivity in Ro52/TRIM21-deficient mice |
title_fullStr | Vicious circle: systemic autoreactivity in Ro52/TRIM21-deficient mice |
title_full_unstemmed | Vicious circle: systemic autoreactivity in Ro52/TRIM21-deficient mice |
title_short | Vicious circle: systemic autoreactivity in Ro52/TRIM21-deficient mice |
title_sort | vicious circle: systemic autoreactivity in ro52/trim21-deficient mice |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722177/ https://www.ncbi.nlm.nih.gov/pubmed/19635865 http://dx.doi.org/10.1084/jem.20091507 |
work_keys_str_mv | AT bollandsilvia viciouscirclesystemicautoreactivityinro52trim21deficientmice AT garciasastreadolfo viciouscirclesystemicautoreactivityinro52trim21deficientmice |