The effect of rhinovirus on airway inflammation in a murine asthma model

PurposeThe aim of the present study was to investigate the differences in lower airway inflammatory immune responses, including cellular responses and responses in terms of inflammatory mediators in bronchoalveolar lavage fluid (BALF) and the airway, to rhinovirus (RV) infection on asthma exacerbati...

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Main Authors: Eugene Kim, Huisu Lee, Hyun Sook Kim, Sulmui Won, Eu Kyoung Lee, Hwan Soo Kim, Kyongwon Bang, Yoon Hong Chun, Jong-Seo Yoon, Hyun Hee Kim, Jin Tack Kim, Joon Sung Lee
Format: Article
Language:English
Published: Korean Pediatric Society 2013-11-01
Series:Korean Journal of Pediatrics
Subjects:
Online Access:http://kjp.or.kr/upload/pdf/kjped-56-482.pdf
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author Eugene Kim
Huisu Lee
Hyun Sook Kim
Sulmui Won
Eu Kyoung Lee
Hwan Soo Kim
Kyongwon Bang
Yoon Hong Chun
Jong-Seo Yoon
Hyun Hee Kim
Jin Tack Kim
Joon Sung Lee
author_facet Eugene Kim
Huisu Lee
Hyun Sook Kim
Sulmui Won
Eu Kyoung Lee
Hwan Soo Kim
Kyongwon Bang
Yoon Hong Chun
Jong-Seo Yoon
Hyun Hee Kim
Jin Tack Kim
Joon Sung Lee
author_sort Eugene Kim
collection DOAJ
description PurposeThe aim of the present study was to investigate the differences in lower airway inflammatory immune responses, including cellular responses and responses in terms of inflammatory mediators in bronchoalveolar lavage fluid (BALF) and the airway, to rhinovirus (RV) infection on asthma exacerbation by comparing a control and a murine asthma model, with or without RV infection.MethodsBALB/c mice were intraperitoneally injected with a crude extract of Dermatophagoides farinae (Df) or phosphate buffered saline (PBS) and were subsequently intranasally treated with a crude extract of Df or PBS. Airway responsiveness and cell infiltration, differential cell counts in BALF, and cytokine and chemokine concentrations in BALF were measured 24 hours after intranasal RV1B infection.ResultsRV infection increased the enhanced pause (Penh) in both the Df sensitized and challenged mice (Df mice) and PBS-treated mice (PBS mice) (P<0.05). Airway eosinophil infiltration increased in Df mice after RV infection (P<0.05). The levels of interleukin (IL) 13, tumor necrosis factor alpha, and regulated on activation, normal T cells expressed and secreted (RANTES) increased in response to RV infection in Df mice, but not in PBS mice (P<0.05). The level of IL-10 significantly decreased following RV infection in Df mice (P<0.05).ConclusionOur findings suggest that the augmented induction of proinflammatory cytokines, Th2 cytokines, and chemokines that mediate an eosinophil response and the decreased induction of regulatory cytokines after RV infection may be important manifestations leading to airway inflammation with eosinophil infiltration and changes in airway responsiveness in the asthma model.
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spelling doaj.art-5e17b0f0a7914a12993990038d9ea2922022-12-22T00:36:53ZengKorean Pediatric SocietyKorean Journal of Pediatrics1738-10612092-72582013-11-01561148248910.3345/kjp.2013.56.11.4822013600042The effect of rhinovirus on airway inflammation in a murine asthma modelEugene Kim0Huisu Lee1Hyun Sook Kim2Sulmui Won3Eu Kyoung Lee4Hwan Soo Kim5Kyongwon Bang6Yoon Hong Chun7Jong-Seo Yoon8Hyun Hee Kim9Jin Tack Kim10Joon Sung Lee11Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.Department of Pediatrics, The Catholic University of Korea College of Medicine, Seoul, Korea.PurposeThe aim of the present study was to investigate the differences in lower airway inflammatory immune responses, including cellular responses and responses in terms of inflammatory mediators in bronchoalveolar lavage fluid (BALF) and the airway, to rhinovirus (RV) infection on asthma exacerbation by comparing a control and a murine asthma model, with or without RV infection.MethodsBALB/c mice were intraperitoneally injected with a crude extract of Dermatophagoides farinae (Df) or phosphate buffered saline (PBS) and were subsequently intranasally treated with a crude extract of Df or PBS. Airway responsiveness and cell infiltration, differential cell counts in BALF, and cytokine and chemokine concentrations in BALF were measured 24 hours after intranasal RV1B infection.ResultsRV infection increased the enhanced pause (Penh) in both the Df sensitized and challenged mice (Df mice) and PBS-treated mice (PBS mice) (P<0.05). Airway eosinophil infiltration increased in Df mice after RV infection (P<0.05). The levels of interleukin (IL) 13, tumor necrosis factor alpha, and regulated on activation, normal T cells expressed and secreted (RANTES) increased in response to RV infection in Df mice, but not in PBS mice (P<0.05). The level of IL-10 significantly decreased following RV infection in Df mice (P<0.05).ConclusionOur findings suggest that the augmented induction of proinflammatory cytokines, Th2 cytokines, and chemokines that mediate an eosinophil response and the decreased induction of regulatory cytokines after RV infection may be important manifestations leading to airway inflammation with eosinophil infiltration and changes in airway responsiveness in the asthma model.http://kjp.or.kr/upload/pdf/kjped-56-482.pdfImmune responseRhinovirusAsthmaExacerbation
spellingShingle Eugene Kim
Huisu Lee
Hyun Sook Kim
Sulmui Won
Eu Kyoung Lee
Hwan Soo Kim
Kyongwon Bang
Yoon Hong Chun
Jong-Seo Yoon
Hyun Hee Kim
Jin Tack Kim
Joon Sung Lee
The effect of rhinovirus on airway inflammation in a murine asthma model
Korean Journal of Pediatrics
Immune response
Rhinovirus
Asthma
Exacerbation
title The effect of rhinovirus on airway inflammation in a murine asthma model
title_full The effect of rhinovirus on airway inflammation in a murine asthma model
title_fullStr The effect of rhinovirus on airway inflammation in a murine asthma model
title_full_unstemmed The effect of rhinovirus on airway inflammation in a murine asthma model
title_short The effect of rhinovirus on airway inflammation in a murine asthma model
title_sort effect of rhinovirus on airway inflammation in a murine asthma model
topic Immune response
Rhinovirus
Asthma
Exacerbation
url http://kjp.or.kr/upload/pdf/kjped-56-482.pdf
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