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Usp18 Driven Enforced Viral Replication in Dendritic Cells Contributes to Break of Immunological Tolerance in Autoimmune Diabetes
Infection with viruses carrying cross-reactive antigens is associated with break of immunological tolerance and induction of autoimmune disease. Dendritic cells play an important role in this process. However, it remains unclear why autoimmune-tolerance is broken during virus infection, but usually...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812017/ https://www.ncbi.nlm.nih.gov/pubmed/24204252 http://dx.doi.org/10.1371/journal.ppat.1003650 |
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author | Honke, Nadine Shaabani, Namir Zhang, Dong-Er Iliakis, George Xu, Haifeng C. Häussinger, Dieter Recher, Mike Löhning, Max Lang, Philipp A. Lang, Karl S. |
author_facet | Honke, Nadine Shaabani, Namir Zhang, Dong-Er Iliakis, George Xu, Haifeng C. Häussinger, Dieter Recher, Mike Löhning, Max Lang, Philipp A. Lang, Karl S. |
author_sort | Honke, Nadine |
collection | PubMed |
description | Infection with viruses carrying cross-reactive antigens is associated with break of immunological tolerance and induction of autoimmune disease. Dendritic cells play an important role in this process. However, it remains unclear why autoimmune-tolerance is broken during virus infection, but usually not during exposure to non-replicating cross-reactive antigens. Here we show that antigen derived from replicating virus but not from non-replicating sources undergoes a multiplication process in dendritic cells in spleen and lymph nodes. This enforced viral replication was dependent on Usp18 and was essential for expansion of autoreactive CD8(+) T cells. Preventing enforced virus replication by depletion of CD11c(+) cells, genetically deleting Usp18, or pharmacologically inhibiting of viral replication blunted the expansion of autoreactive CD8(+) T cells and prevented autoimmune diabetes. In conclusion, Usp18-driven enforced viral replication in dendritic cells can break immunological tolerance and critically influences induction of autoimmunity. |
format | Online Article Text |
id | pubmed-3812017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38120172013-11-07 Usp18 Driven Enforced Viral Replication in Dendritic Cells Contributes to Break of Immunological Tolerance in Autoimmune Diabetes Honke, Nadine Shaabani, Namir Zhang, Dong-Er Iliakis, George Xu, Haifeng C. Häussinger, Dieter Recher, Mike Löhning, Max Lang, Philipp A. Lang, Karl S. PLoS Pathog Research Article Infection with viruses carrying cross-reactive antigens is associated with break of immunological tolerance and induction of autoimmune disease. Dendritic cells play an important role in this process. However, it remains unclear why autoimmune-tolerance is broken during virus infection, but usually not during exposure to non-replicating cross-reactive antigens. Here we show that antigen derived from replicating virus but not from non-replicating sources undergoes a multiplication process in dendritic cells in spleen and lymph nodes. This enforced viral replication was dependent on Usp18 and was essential for expansion of autoreactive CD8(+) T cells. Preventing enforced virus replication by depletion of CD11c(+) cells, genetically deleting Usp18, or pharmacologically inhibiting of viral replication blunted the expansion of autoreactive CD8(+) T cells and prevented autoimmune diabetes. In conclusion, Usp18-driven enforced viral replication in dendritic cells can break immunological tolerance and critically influences induction of autoimmunity. Public Library of Science 2013-10-24 /pmc/articles/PMC3812017/ /pubmed/24204252 http://dx.doi.org/10.1371/journal.ppat.1003650 Text en © 2013 Honke et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Honke, Nadine Shaabani, Namir Zhang, Dong-Er Iliakis, George Xu, Haifeng C. Häussinger, Dieter Recher, Mike Löhning, Max Lang, Philipp A. Lang, Karl S. Usp18 Driven Enforced Viral Replication in Dendritic Cells Contributes to Break of Immunological Tolerance in Autoimmune Diabetes |
title |
Usp18 Driven Enforced Viral Replication in Dendritic Cells Contributes to Break of Immunological Tolerance in Autoimmune Diabetes |
title_full |
Usp18 Driven Enforced Viral Replication in Dendritic Cells Contributes to Break of Immunological Tolerance in Autoimmune Diabetes |
title_fullStr |
Usp18 Driven Enforced Viral Replication in Dendritic Cells Contributes to Break of Immunological Tolerance in Autoimmune Diabetes |
title_full_unstemmed |
Usp18 Driven Enforced Viral Replication in Dendritic Cells Contributes to Break of Immunological Tolerance in Autoimmune Diabetes |
title_short |
Usp18 Driven Enforced Viral Replication in Dendritic Cells Contributes to Break of Immunological Tolerance in Autoimmune Diabetes |
title_sort | usp18 driven enforced viral replication in dendritic cells contributes to break of immunological tolerance in autoimmune diabetes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812017/ https://www.ncbi.nlm.nih.gov/pubmed/24204252 http://dx.doi.org/10.1371/journal.ppat.1003650 |
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