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T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients

BACKGROUND: Chronic rhinosinusitis with nasal polyps is characterized by local inflammation and is categorized into two subtypes in Japan: eosinophilic chronic rhinosinusitis, and non-eosinophilic chronic rhinosinusitis. The objective of this study was to investigate the expression of key transcript...

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Autores principales: Baba, Shintaro, Kagoya, Ryoji, Kondo, Kenji, Suzukawa, Maho, Ohta, Ken, Yamasoba, Tatsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4653844/
https://www.ncbi.nlm.nih.gov/pubmed/26594227
http://dx.doi.org/10.1186/s13223-015-0100-2
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author Baba, Shintaro
Kagoya, Ryoji
Kondo, Kenji
Suzukawa, Maho
Ohta, Ken
Yamasoba, Tatsuya
author_facet Baba, Shintaro
Kagoya, Ryoji
Kondo, Kenji
Suzukawa, Maho
Ohta, Ken
Yamasoba, Tatsuya
author_sort Baba, Shintaro
collection PubMed
description BACKGROUND: Chronic rhinosinusitis with nasal polyps is characterized by local inflammation and is categorized into two subtypes in Japan: eosinophilic chronic rhinosinusitis, and non-eosinophilic chronic rhinosinusitis. The objective of this study was to investigate the expression of key transcription factors for Treg and Th1/Th2/Th17 cells, in relation to the mRNA expression of representative cytokines in these two subtypes of chronic rhinosinusitis with nasal polyps. METHODS: The expression of forkhead box P3 (FOXP3), T-box transcription factor (T-bet), GATA3, retinoid acid-related orphan receptor C (RORc), the suppressive cytokines TGF-β1 and IL-10, and Th1/Th2/Th17 cytokines (IFN-γ, IL-4, IL-5, IL-13, IL-17) were analyzed by means of RT-PCR in eosinophilic polyps. Eosinophilic polyps were defined as having an eosinophil count of more than 50 per microscopic field (×400 magnification) using five fields located in the subepithelial area of the polyps, while the non-eosinophilic polyps and controls did not fulfill this criteria. The numbers of T cells, CD4+ T cells, CD8+ T cells and Treg were histologically counted using sections that were immunostained for CD3, CD4, CD8, and FOXP3, respectively. RESULTS: In eosinophilic polyps, we observed significantly fewer CD4+ T cells and CD8+ T cells, and lower GATA3, RORc and IL-10 mRNA expression, but a significantly higher IL-5, and IL-13 mRNA expression compared with controls, whereas FOXP3 and T-bet mRNA expression were not significantly different compared with controls. In non-eosinophilic polyps, FOXP3, IL-10, IL-17A, TGFβ1 and IFNγ mRNA expression was significantly higher compared with controls, whereas IL-4, 5 and 13 expression was not significantly different from controls. CONCLUSION: We showed a reduction of GATA3 and RORc mRNA, low Treg-related cytokines and elevated Th2 cytokine levels in eosinophilic chronic rhinosinusitis, whereas we demonstrated the upregulation of Treg cells and increases of Th1 and Th17 cytokines in non-eosinophilic chronic rhinosinusitis in the Japanese population. The different mRNA expression profiles of Treg and Th1/Th2/Th17 signature transcription factors and cytokines between eosinophilic chronic rhinosinusitis and non-eosinophilic chronic rhinosinusitis suggests heterogeneity in the pathogenesis of chronic rhinosinusitis with nasal polyps.
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spelling pubmed-46538442015-11-21 T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients Baba, Shintaro Kagoya, Ryoji Kondo, Kenji Suzukawa, Maho Ohta, Ken Yamasoba, Tatsuya Allergy Asthma Clin Immunol Research BACKGROUND: Chronic rhinosinusitis with nasal polyps is characterized by local inflammation and is categorized into two subtypes in Japan: eosinophilic chronic rhinosinusitis, and non-eosinophilic chronic rhinosinusitis. The objective of this study was to investigate the expression of key transcription factors for Treg and Th1/Th2/Th17 cells, in relation to the mRNA expression of representative cytokines in these two subtypes of chronic rhinosinusitis with nasal polyps. METHODS: The expression of forkhead box P3 (FOXP3), T-box transcription factor (T-bet), GATA3, retinoid acid-related orphan receptor C (RORc), the suppressive cytokines TGF-β1 and IL-10, and Th1/Th2/Th17 cytokines (IFN-γ, IL-4, IL-5, IL-13, IL-17) were analyzed by means of RT-PCR in eosinophilic polyps. Eosinophilic polyps were defined as having an eosinophil count of more than 50 per microscopic field (×400 magnification) using five fields located in the subepithelial area of the polyps, while the non-eosinophilic polyps and controls did not fulfill this criteria. The numbers of T cells, CD4+ T cells, CD8+ T cells and Treg were histologically counted using sections that were immunostained for CD3, CD4, CD8, and FOXP3, respectively. RESULTS: In eosinophilic polyps, we observed significantly fewer CD4+ T cells and CD8+ T cells, and lower GATA3, RORc and IL-10 mRNA expression, but a significantly higher IL-5, and IL-13 mRNA expression compared with controls, whereas FOXP3 and T-bet mRNA expression were not significantly different compared with controls. In non-eosinophilic polyps, FOXP3, IL-10, IL-17A, TGFβ1 and IFNγ mRNA expression was significantly higher compared with controls, whereas IL-4, 5 and 13 expression was not significantly different from controls. CONCLUSION: We showed a reduction of GATA3 and RORc mRNA, low Treg-related cytokines and elevated Th2 cytokine levels in eosinophilic chronic rhinosinusitis, whereas we demonstrated the upregulation of Treg cells and increases of Th1 and Th17 cytokines in non-eosinophilic chronic rhinosinusitis in the Japanese population. The different mRNA expression profiles of Treg and Th1/Th2/Th17 signature transcription factors and cytokines between eosinophilic chronic rhinosinusitis and non-eosinophilic chronic rhinosinusitis suggests heterogeneity in the pathogenesis of chronic rhinosinusitis with nasal polyps. BioMed Central 2015-11-19 /pmc/articles/PMC4653844/ /pubmed/26594227 http://dx.doi.org/10.1186/s13223-015-0100-2 Text en © Baba et al. 2015 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
Baba, Shintaro
Kagoya, Ryoji
Kondo, Kenji
Suzukawa, Maho
Ohta, Ken
Yamasoba, Tatsuya
T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients
title T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients
title_full T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients
title_fullStr T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients
title_full_unstemmed T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients
title_short T-cell phenotypes in chronic rhinosinusitis with nasal polyps in Japanese patients
title_sort t-cell phenotypes in chronic rhinosinusitis with nasal polyps in japanese patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4653844/
https://www.ncbi.nlm.nih.gov/pubmed/26594227
http://dx.doi.org/10.1186/s13223-015-0100-2
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