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Impact of Chronic Rhinosinusitis with Nasal Polyposis on IL-12 and IL-8

INTRODUCTION: The pathophysiology of Chronic Rhinosinusitis is coordinated by distinct inflammatory reactions in different individuals. Inflammatory environments with a predominance of Th2 lymphocytes tend also to be rich in eosinophils. These environments are common during the formation of nasal po...

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Autores principales: do Amaral, Janatas Bussador, David, Andrea Goldwasser, Mello, Luciane, Bachi, Andre Luis Lacerda, Voegels, Richard Louis, Thamboo, Andrew, Pezato, Rogério
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872264/
https://www.ncbi.nlm.nih.gov/pubmed/36721412
http://dx.doi.org/10.22038/IJORL.2022.53663.2829
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author do Amaral, Janatas Bussador
David, Andrea Goldwasser
Mello, Luciane
Bachi, Andre Luis Lacerda
Voegels, Richard Louis
Thamboo, Andrew
Pezato, Rogério
author_facet do Amaral, Janatas Bussador
David, Andrea Goldwasser
Mello, Luciane
Bachi, Andre Luis Lacerda
Voegels, Richard Louis
Thamboo, Andrew
Pezato, Rogério
author_sort do Amaral, Janatas Bussador
collection PubMed
description INTRODUCTION: The pathophysiology of Chronic Rhinosinusitis is coordinated by distinct inflammatory reactions in different individuals. Inflammatory environments with a predominance of Th2 lymphocytes tend also to be rich in eosinophils. These environments are common during the formation of nasal polyps associated with aspirin intolerance, which is also marked by an increase in inflammatory mediators, especially IL-4, IL-5, and IL-13. Despite the significance of these inflammatory mediators, the relevance of IL-12 subunits' presence within eosinophilic nasal polyps, however, has been less studied. The current study aims to evaluate the presence of IL-12 subunits, IL-12p40 and IL-12p70, in eosinophilic nasal polyps and their correlations with IL-8 presence. MATERIALS AND METHODS: We compared the concentrations of IL-8, IL12p40, and IL12p70 among samples of eosinophilic nasal polypoid tissue, eosinophilic nasal polypoid tissue associated with aspirin intolerance, and healthy nasal mucosa, using an indirect immunoassay (ELISA) kit. RESULTS: When compared to healthy nasal mucosa, there was a lower concentration of IL-8 in Chronic Rhinosinusitis with Nasal Polyp (CRSwNP) tissue. Aspirin Intolerant polypoid tissue also presented a lower concentration of IL-12 subunits compared to healthy nasal mucosa. There was no significant correlation between IL-8 and IL-12 in the eosinophilic polypoid conditions. CONCLUSION: In CRSwNP, there is a reduction in IL-8 and IL-12 subunits compared to control, with a lack of correlation between IL-12 and IL-8. The lack of correlation can be justified by a type two inflammatory storm environment.
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spelling pubmed-98722642023-01-30 Impact of Chronic Rhinosinusitis with Nasal Polyposis on IL-12 and IL-8 do Amaral, Janatas Bussador David, Andrea Goldwasser Mello, Luciane Bachi, Andre Luis Lacerda Voegels, Richard Louis Thamboo, Andrew Pezato, Rogério Iran J Otorhinolaryngol Original Article INTRODUCTION: The pathophysiology of Chronic Rhinosinusitis is coordinated by distinct inflammatory reactions in different individuals. Inflammatory environments with a predominance of Th2 lymphocytes tend also to be rich in eosinophils. These environments are common during the formation of nasal polyps associated with aspirin intolerance, which is also marked by an increase in inflammatory mediators, especially IL-4, IL-5, and IL-13. Despite the significance of these inflammatory mediators, the relevance of IL-12 subunits' presence within eosinophilic nasal polyps, however, has been less studied. The current study aims to evaluate the presence of IL-12 subunits, IL-12p40 and IL-12p70, in eosinophilic nasal polyps and their correlations with IL-8 presence. MATERIALS AND METHODS: We compared the concentrations of IL-8, IL12p40, and IL12p70 among samples of eosinophilic nasal polypoid tissue, eosinophilic nasal polypoid tissue associated with aspirin intolerance, and healthy nasal mucosa, using an indirect immunoassay (ELISA) kit. RESULTS: When compared to healthy nasal mucosa, there was a lower concentration of IL-8 in Chronic Rhinosinusitis with Nasal Polyp (CRSwNP) tissue. Aspirin Intolerant polypoid tissue also presented a lower concentration of IL-12 subunits compared to healthy nasal mucosa. There was no significant correlation between IL-8 and IL-12 in the eosinophilic polypoid conditions. CONCLUSION: In CRSwNP, there is a reduction in IL-8 and IL-12 subunits compared to control, with a lack of correlation between IL-12 and IL-8. The lack of correlation can be justified by a type two inflammatory storm environment. Mashhad University of Medical Sciences 2023-01 /pmc/articles/PMC9872264/ /pubmed/36721412 http://dx.doi.org/10.22038/IJORL.2022.53663.2829 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
do Amaral, Janatas Bussador
David, Andrea Goldwasser
Mello, Luciane
Bachi, Andre Luis Lacerda
Voegels, Richard Louis
Thamboo, Andrew
Pezato, Rogério
Impact of Chronic Rhinosinusitis with Nasal Polyposis on IL-12 and IL-8
title Impact of Chronic Rhinosinusitis with Nasal Polyposis on IL-12 and IL-8
title_full Impact of Chronic Rhinosinusitis with Nasal Polyposis on IL-12 and IL-8
title_fullStr Impact of Chronic Rhinosinusitis with Nasal Polyposis on IL-12 and IL-8
title_full_unstemmed Impact of Chronic Rhinosinusitis with Nasal Polyposis on IL-12 and IL-8
title_short Impact of Chronic Rhinosinusitis with Nasal Polyposis on IL-12 and IL-8
title_sort impact of chronic rhinosinusitis with nasal polyposis on il-12 and il-8
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872264/
https://www.ncbi.nlm.nih.gov/pubmed/36721412
http://dx.doi.org/10.22038/IJORL.2022.53663.2829
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