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Dysregulated TGF-β Production Underlies the Age-Related Vulnerability to Chikungunya Virus
Chikungunya virus (CHIKV) is a re-emerging global pathogen with pandemic potential, which causes fever, rash and debilitating arthralgia. Older adults over 65 years are particularly susceptible to severe and chronic CHIKV disease (CHIKVD), accounting for >90% of all CHIKV-related deaths. There ar...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063327/ https://www.ncbi.nlm.nih.gov/pubmed/27736984 http://dx.doi.org/10.1371/journal.ppat.1005891 |
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author | Uhrlaub, Jennifer L. Pulko, Vesna DeFilippis, Victor R. Broeckel, Rebecca Streblow, Daniel N. Coleman, Gary D. Park, Byung S. Lindo, John F. Vickers, Ivan Anzinger, Joshua J. Nikolich-Žugich, Janko |
author_facet | Uhrlaub, Jennifer L. Pulko, Vesna DeFilippis, Victor R. Broeckel, Rebecca Streblow, Daniel N. Coleman, Gary D. Park, Byung S. Lindo, John F. Vickers, Ivan Anzinger, Joshua J. Nikolich-Žugich, Janko |
author_sort | Uhrlaub, Jennifer L. |
collection | PubMed |
description | Chikungunya virus (CHIKV) is a re-emerging global pathogen with pandemic potential, which causes fever, rash and debilitating arthralgia. Older adults over 65 years are particularly susceptible to severe and chronic CHIKV disease (CHIKVD), accounting for >90% of all CHIKV-related deaths. There are currently no approved vaccines or antiviral treatments available to limit chronic CHIKVD. Here we show that in old mice excessive, dysregulated TGFβ production during acute infection leads to a reduced immune response and subsequent chronic disease. Humans suffering from CHIKV infection also exhibited high TGFβ levels and a pronounced age-related defect in neutralizing anti-CHIKV antibody production. In vivo reduction of TGFβ levels minimized acute joint swelling, restored neutralizing antibody production and diminished chronic joint pathology in old mice. This study identifies increased and dysregulated TGFβ secretion as one key mechanism contributing to the age-related loss of protective anti-CHIKV-immunity leading to chronic CHIKVD. |
format | Online Article Text |
id | pubmed-5063327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50633272016-11-04 Dysregulated TGF-β Production Underlies the Age-Related Vulnerability to Chikungunya Virus Uhrlaub, Jennifer L. Pulko, Vesna DeFilippis, Victor R. Broeckel, Rebecca Streblow, Daniel N. Coleman, Gary D. Park, Byung S. Lindo, John F. Vickers, Ivan Anzinger, Joshua J. Nikolich-Žugich, Janko PLoS Pathog Research Article Chikungunya virus (CHIKV) is a re-emerging global pathogen with pandemic potential, which causes fever, rash and debilitating arthralgia. Older adults over 65 years are particularly susceptible to severe and chronic CHIKV disease (CHIKVD), accounting for >90% of all CHIKV-related deaths. There are currently no approved vaccines or antiviral treatments available to limit chronic CHIKVD. Here we show that in old mice excessive, dysregulated TGFβ production during acute infection leads to a reduced immune response and subsequent chronic disease. Humans suffering from CHIKV infection also exhibited high TGFβ levels and a pronounced age-related defect in neutralizing anti-CHIKV antibody production. In vivo reduction of TGFβ levels minimized acute joint swelling, restored neutralizing antibody production and diminished chronic joint pathology in old mice. This study identifies increased and dysregulated TGFβ secretion as one key mechanism contributing to the age-related loss of protective anti-CHIKV-immunity leading to chronic CHIKVD. Public Library of Science 2016-10-13 /pmc/articles/PMC5063327/ /pubmed/27736984 http://dx.doi.org/10.1371/journal.ppat.1005891 Text en © 2016 Uhrlaub 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 Uhrlaub, Jennifer L. Pulko, Vesna DeFilippis, Victor R. Broeckel, Rebecca Streblow, Daniel N. Coleman, Gary D. Park, Byung S. Lindo, John F. Vickers, Ivan Anzinger, Joshua J. Nikolich-Žugich, Janko Dysregulated TGF-β Production Underlies the Age-Related Vulnerability to Chikungunya Virus |
title | Dysregulated TGF-β Production Underlies the Age-Related Vulnerability to Chikungunya Virus |
title_full | Dysregulated TGF-β Production Underlies the Age-Related Vulnerability to Chikungunya Virus |
title_fullStr | Dysregulated TGF-β Production Underlies the Age-Related Vulnerability to Chikungunya Virus |
title_full_unstemmed | Dysregulated TGF-β Production Underlies the Age-Related Vulnerability to Chikungunya Virus |
title_short | Dysregulated TGF-β Production Underlies the Age-Related Vulnerability to Chikungunya Virus |
title_sort | dysregulated tgf-β production underlies the age-related vulnerability to chikungunya virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063327/ https://www.ncbi.nlm.nih.gov/pubmed/27736984 http://dx.doi.org/10.1371/journal.ppat.1005891 |
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