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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
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.
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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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