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Influence of viral infection on the relationships between airway cytokines and lung function in asthmatic children

BACKGROUND: Few longitudinal studies examine inflammation and lung function in asthma. We sought to determine the cytokines that reduce airflow, and the influence of respiratory viral infections on these relationships. METHODS: Children underwent home collections of nasal lavage during scheduled sur...

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Autores principales: Lewis, Toby C., Metitiri, Ediri E., Mentz, Graciela B., Ren, Xiaodan, Carpenter, Ashley R., Goldsmith, Adam M., Wicklund, Kyra E., Eder, Breanna N., Comstock, Adam T., Ricci, Jeannette M., Brennan, Sean R., Washington, Ginger L., Owens, Kendall B., Mukherjee, Bhramar, Robins, Thomas G., Batterman, Stuart A., Hershenson, Marc B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249926/
https://www.ncbi.nlm.nih.gov/pubmed/30463560
http://dx.doi.org/10.1186/s12931-018-0922-9
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author Lewis, Toby C.
Metitiri, Ediri E.
Mentz, Graciela B.
Ren, Xiaodan
Carpenter, Ashley R.
Goldsmith, Adam M.
Wicklund, Kyra E.
Eder, Breanna N.
Comstock, Adam T.
Ricci, Jeannette M.
Brennan, Sean R.
Washington, Ginger L.
Owens, Kendall B.
Mukherjee, Bhramar
Robins, Thomas G.
Batterman, Stuart A.
Hershenson, Marc B.
author_facet Lewis, Toby C.
Metitiri, Ediri E.
Mentz, Graciela B.
Ren, Xiaodan
Carpenter, Ashley R.
Goldsmith, Adam M.
Wicklund, Kyra E.
Eder, Breanna N.
Comstock, Adam T.
Ricci, Jeannette M.
Brennan, Sean R.
Washington, Ginger L.
Owens, Kendall B.
Mukherjee, Bhramar
Robins, Thomas G.
Batterman, Stuart A.
Hershenson, Marc B.
author_sort Lewis, Toby C.
collection PubMed
description BACKGROUND: Few longitudinal studies examine inflammation and lung function in asthma. We sought to determine the cytokines that reduce airflow, and the influence of respiratory viral infections on these relationships. METHODS: Children underwent home collections of nasal lavage during scheduled surveillance periods and self-reported respiratory illnesses. We studied 53 children for one year, analyzing 392 surveillance samples and 203 samples from 85 respiratory illnesses. Generalized estimated equations were used to evaluate associations between nasal lavage biomarkers (7 mRNAs, 10 proteins), lung function and viral infection. RESULTS: As anticipated, viral infection was associated with increased cytokines and reduced FVC and FEV(1). However, we found frequent and strong interactions between biomarkers and virus on lung function. For example, in the absence of viral infection, CXCL10 mRNA, MDA5 mRNA, CXCL10, IL-4, IL-13, CCL4, CCL5, CCL20 and CCL24 were negatively associated with FVC. In contrast, during infection, the opposite relationship was frequently found, with IL-4, IL-13, CCL5, CCL20 and CCL24 levels associated with less severe reductions in both FVC and FEV(1). CONCLUSIONS: In asthmatic children, airflow obstruction is driven by specific pro-inflammatory cytokines. In the absence of viral infection, higher cytokine levels are associated with decreasing lung function. However, with infection, there is a reversal in this relationship, with cytokine abundance associated with reduced lung function decline. While nasal samples may not reflect lower airway responses, these data suggest that some aspects of the inflammatory response may be protective against viral infection. This study may have ramifications for the treatment of viral-induced asthma exacerbations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0922-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-62499262018-11-26 Influence of viral infection on the relationships between airway cytokines and lung function in asthmatic children Lewis, Toby C. Metitiri, Ediri E. Mentz, Graciela B. Ren, Xiaodan Carpenter, Ashley R. Goldsmith, Adam M. Wicklund, Kyra E. Eder, Breanna N. Comstock, Adam T. Ricci, Jeannette M. Brennan, Sean R. Washington, Ginger L. Owens, Kendall B. Mukherjee, Bhramar Robins, Thomas G. Batterman, Stuart A. Hershenson, Marc B. Respir Res Research BACKGROUND: Few longitudinal studies examine inflammation and lung function in asthma. We sought to determine the cytokines that reduce airflow, and the influence of respiratory viral infections on these relationships. METHODS: Children underwent home collections of nasal lavage during scheduled surveillance periods and self-reported respiratory illnesses. We studied 53 children for one year, analyzing 392 surveillance samples and 203 samples from 85 respiratory illnesses. Generalized estimated equations were used to evaluate associations between nasal lavage biomarkers (7 mRNAs, 10 proteins), lung function and viral infection. RESULTS: As anticipated, viral infection was associated with increased cytokines and reduced FVC and FEV(1). However, we found frequent and strong interactions between biomarkers and virus on lung function. For example, in the absence of viral infection, CXCL10 mRNA, MDA5 mRNA, CXCL10, IL-4, IL-13, CCL4, CCL5, CCL20 and CCL24 were negatively associated with FVC. In contrast, during infection, the opposite relationship was frequently found, with IL-4, IL-13, CCL5, CCL20 and CCL24 levels associated with less severe reductions in both FVC and FEV(1). CONCLUSIONS: In asthmatic children, airflow obstruction is driven by specific pro-inflammatory cytokines. In the absence of viral infection, higher cytokine levels are associated with decreasing lung function. However, with infection, there is a reversal in this relationship, with cytokine abundance associated with reduced lung function decline. While nasal samples may not reflect lower airway responses, these data suggest that some aspects of the inflammatory response may be protective against viral infection. This study may have ramifications for the treatment of viral-induced asthma exacerbations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0922-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-21 2018 /pmc/articles/PMC6249926/ /pubmed/30463560 http://dx.doi.org/10.1186/s12931-018-0922-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lewis, Toby C.
Metitiri, Ediri E.
Mentz, Graciela B.
Ren, Xiaodan
Carpenter, Ashley R.
Goldsmith, Adam M.
Wicklund, Kyra E.
Eder, Breanna N.
Comstock, Adam T.
Ricci, Jeannette M.
Brennan, Sean R.
Washington, Ginger L.
Owens, Kendall B.
Mukherjee, Bhramar
Robins, Thomas G.
Batterman, Stuart A.
Hershenson, Marc B.
Influence of viral infection on the relationships between airway cytokines and lung function in asthmatic children
title Influence of viral infection on the relationships between airway cytokines and lung function in asthmatic children
title_full Influence of viral infection on the relationships between airway cytokines and lung function in asthmatic children
title_fullStr Influence of viral infection on the relationships between airway cytokines and lung function in asthmatic children
title_full_unstemmed Influence of viral infection on the relationships between airway cytokines and lung function in asthmatic children
title_short Influence of viral infection on the relationships between airway cytokines and lung function in asthmatic children
title_sort influence of viral infection on the relationships between airway cytokines and lung function in asthmatic children
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249926/
https://www.ncbi.nlm.nih.gov/pubmed/30463560
http://dx.doi.org/10.1186/s12931-018-0922-9
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