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IL-33/ST2 immune responses to respiratory bacteria in pediatric asthma
Here we investigated the relationship between local bacterial colonization and anti-bacterial immune responses in pre-school asthmatic and control children within the EU-wide study PreDicta. In this cohort of pre-school asthmatic children, nasopharyngeal colonization with Gram-negative bacteria such...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338274/ https://www.ncbi.nlm.nih.gov/pubmed/28262704 http://dx.doi.org/10.1038/srep43426 |
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author | Hentschke, Isabell Graser, Anna Melichar, Volker O. Kiefer, Alexander Zimmermann, Theodor Kroß, Bettina Haag, Patricia Xepapadaki, Paraskevi Papadopoulos, Nikolaos G. Bogdan, Christian Finotto, Susetta |
author_facet | Hentschke, Isabell Graser, Anna Melichar, Volker O. Kiefer, Alexander Zimmermann, Theodor Kroß, Bettina Haag, Patricia Xepapadaki, Paraskevi Papadopoulos, Nikolaos G. Bogdan, Christian Finotto, Susetta |
author_sort | Hentschke, Isabell |
collection | PubMed |
description | Here we investigated the relationship between local bacterial colonization and anti-bacterial immune responses in pre-school asthmatic and control children within the EU-wide study PreDicta. In this cohort of pre-school asthmatic children, nasopharyngeal colonization with Gram-negative bacteria such as Haemophilus influenzae and Moraxella catarrhalis was found to be associated with the highest interferon beta (IFNβ) and IL-33 levels in the nasal pharyngeal fluids (NPF). IL33R-ST2 was found induced in the blood of asthmatic children with additional Gram + bacteria in the nasopharynx (Gr+/−). Furthermore, asthmatic children had more episodes of infection that required antibiotic therapy than the control group. Treatment with antibiotics associated with reduced ST2 in blood cells of both asthmatic and control children and reduced IL-33 levels in the airways of asthmatic children. In the absence of Staphylococcus (S.) aureus in NPF, antibiotic therapy associated with decreased IL-33 levels in the NPF and lower ST2 values in the blood of control children but not of asthmatic children. These data suggest that, in asthmatic children, Gram- bacteria, which persist after antibiotic therapy, contributes to IL-33 locally and associated with Gr + bacteria colonization in the airways, inhibited IFN-β and in the absence of Staphylococcus (S.) aureus, induced ST2 bearing cells in their blood. |
format | Online Article Text |
id | pubmed-5338274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53382742017-03-08 IL-33/ST2 immune responses to respiratory bacteria in pediatric asthma Hentschke, Isabell Graser, Anna Melichar, Volker O. Kiefer, Alexander Zimmermann, Theodor Kroß, Bettina Haag, Patricia Xepapadaki, Paraskevi Papadopoulos, Nikolaos G. Bogdan, Christian Finotto, Susetta Sci Rep Article Here we investigated the relationship between local bacterial colonization and anti-bacterial immune responses in pre-school asthmatic and control children within the EU-wide study PreDicta. In this cohort of pre-school asthmatic children, nasopharyngeal colonization with Gram-negative bacteria such as Haemophilus influenzae and Moraxella catarrhalis was found to be associated with the highest interferon beta (IFNβ) and IL-33 levels in the nasal pharyngeal fluids (NPF). IL33R-ST2 was found induced in the blood of asthmatic children with additional Gram + bacteria in the nasopharynx (Gr+/−). Furthermore, asthmatic children had more episodes of infection that required antibiotic therapy than the control group. Treatment with antibiotics associated with reduced ST2 in blood cells of both asthmatic and control children and reduced IL-33 levels in the airways of asthmatic children. In the absence of Staphylococcus (S.) aureus in NPF, antibiotic therapy associated with decreased IL-33 levels in the NPF and lower ST2 values in the blood of control children but not of asthmatic children. These data suggest that, in asthmatic children, Gram- bacteria, which persist after antibiotic therapy, contributes to IL-33 locally and associated with Gr + bacteria colonization in the airways, inhibited IFN-β and in the absence of Staphylococcus (S.) aureus, induced ST2 bearing cells in their blood. Nature Publishing Group 2017-03-06 /pmc/articles/PMC5338274/ /pubmed/28262704 http://dx.doi.org/10.1038/srep43426 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hentschke, Isabell Graser, Anna Melichar, Volker O. Kiefer, Alexander Zimmermann, Theodor Kroß, Bettina Haag, Patricia Xepapadaki, Paraskevi Papadopoulos, Nikolaos G. Bogdan, Christian Finotto, Susetta IL-33/ST2 immune responses to respiratory bacteria in pediatric asthma |
title | IL-33/ST2 immune responses to respiratory bacteria in pediatric asthma |
title_full | IL-33/ST2 immune responses to respiratory bacteria in pediatric asthma |
title_fullStr | IL-33/ST2 immune responses to respiratory bacteria in pediatric asthma |
title_full_unstemmed | IL-33/ST2 immune responses to respiratory bacteria in pediatric asthma |
title_short | IL-33/ST2 immune responses to respiratory bacteria in pediatric asthma |
title_sort | il-33/st2 immune responses to respiratory bacteria in pediatric asthma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338274/ https://www.ncbi.nlm.nih.gov/pubmed/28262704 http://dx.doi.org/10.1038/srep43426 |
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