The involvement of IL-17A in the murine response to sub-lethal inhalational infection with Francisella tularensis.

<h4>Background</h4>Francisella tularensis is an intercellular bacterium often causing fatal disease when inhaled. Previous reports have underlined the role of cell-mediated immunity and IFNgamma in the host response to Francisella tularensis infection.<h4>Methodology/principal find...

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Autores principales: Gal Markel, Erez Bar-Haim, Eran Zahavy, Hila Cohen, Ofer Cohen, Avigdor Shafferman, Baruch Velan
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spelling oai:doaj.org-article:52ea3ed01f0e4842ae8bc8b98e357db52021-12-02T20:20:41ZThe involvement of IL-17A in the murine response to sub-lethal inhalational infection with Francisella tularensis.1932-620310.1371/journal.pone.0011176https://doaj.org/article/52ea3ed01f0e4842ae8bc8b98e357db52010-06-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20585449/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Francisella tularensis is an intercellular bacterium often causing fatal disease when inhaled. Previous reports have underlined the role of cell-mediated immunity and IFNgamma in the host response to Francisella tularensis infection.<h4>Methodology/principal findings</h4>Here we provide evidence for the involvement of IL-17A in host defense to inhalational tularemia, using a mouse model of intranasal infection with the Live Vaccine Strain (LVS). We demonstrate the kinetics of IL-17A production in lavage fluids of infected lungs and identify the IL-17A-producing lymphocytes as pulmonary gammadelta and Th17 cells. The peak of IL-17A production appears early during sub-lethal infection, it precedes the peak of immune activation and the nadir of the disease, and then subsides subsequently. Exogenous airway administration of IL-17A or of IL-23 had a limited yet consistent effect of delaying the onset of death from a lethal dose of LVS, implying that IL-17A may be involved in restraining the infection. The protective role for IL-17A was directly demonstrated by in vivo neutralization of IL-17A. Administration of anti IL-17A antibodies concomitantly to a sub-lethal airway infection with 0.1xLD(50) resulted in a fatal disease.<h4>Conclusion</h4>In summary, these data characterize the involvement and underline the protective key role of the IL-17A axis in the lungs from inhalational tularemia.Gal MarkelErez Bar-HaimEran ZahavyHila CohenOfer CohenAvigdor ShaffermanBaruch VelanPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 6, p e11176 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Gal Markel
Erez Bar-Haim
Eran Zahavy
Hila Cohen
Ofer Cohen
Avigdor Shafferman
Baruch Velan
The involvement of IL-17A in the murine response to sub-lethal inhalational infection with Francisella tularensis.
description <h4>Background</h4>Francisella tularensis is an intercellular bacterium often causing fatal disease when inhaled. Previous reports have underlined the role of cell-mediated immunity and IFNgamma in the host response to Francisella tularensis infection.<h4>Methodology/principal findings</h4>Here we provide evidence for the involvement of IL-17A in host defense to inhalational tularemia, using a mouse model of intranasal infection with the Live Vaccine Strain (LVS). We demonstrate the kinetics of IL-17A production in lavage fluids of infected lungs and identify the IL-17A-producing lymphocytes as pulmonary gammadelta and Th17 cells. The peak of IL-17A production appears early during sub-lethal infection, it precedes the peak of immune activation and the nadir of the disease, and then subsides subsequently. Exogenous airway administration of IL-17A or of IL-23 had a limited yet consistent effect of delaying the onset of death from a lethal dose of LVS, implying that IL-17A may be involved in restraining the infection. The protective role for IL-17A was directly demonstrated by in vivo neutralization of IL-17A. Administration of anti IL-17A antibodies concomitantly to a sub-lethal airway infection with 0.1xLD(50) resulted in a fatal disease.<h4>Conclusion</h4>In summary, these data characterize the involvement and underline the protective key role of the IL-17A axis in the lungs from inhalational tularemia.
format article
author Gal Markel
Erez Bar-Haim
Eran Zahavy
Hila Cohen
Ofer Cohen
Avigdor Shafferman
Baruch Velan
author_facet Gal Markel
Erez Bar-Haim
Eran Zahavy
Hila Cohen
Ofer Cohen
Avigdor Shafferman
Baruch Velan
author_sort Gal Markel
title The involvement of IL-17A in the murine response to sub-lethal inhalational infection with Francisella tularensis.
title_short The involvement of IL-17A in the murine response to sub-lethal inhalational infection with Francisella tularensis.
title_full The involvement of IL-17A in the murine response to sub-lethal inhalational infection with Francisella tularensis.
title_fullStr The involvement of IL-17A in the murine response to sub-lethal inhalational infection with Francisella tularensis.
title_full_unstemmed The involvement of IL-17A in the murine response to sub-lethal inhalational infection with Francisella tularensis.
title_sort involvement of il-17a in the murine response to sub-lethal inhalational infection with francisella tularensis.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/52ea3ed01f0e4842ae8bc8b98e357db5
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