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Clinical and Laboratory Studies of the Fate of Intranasal Allergen

BACKGROUND: The precise way in which allergen is handled by the nose is unknown. The objective of this study was to determine recovery of Der p 1 allergen following nasal administration and to determine whether Der p 1 can be detected in nasal biopsies after natural exposure and nasal challenge to a...

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Autores principales: Rimmer, Janet, Santos, Conceição, Yli-Panula, Eija, Noronha, Virginia, Viander, Markku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430540/
https://www.ncbi.nlm.nih.gov/pubmed/25969994
http://dx.doi.org/10.1371/journal.pone.0127477
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author Rimmer, Janet
Santos, Conceição
Yli-Panula, Eija
Noronha, Virginia
Viander, Markku
author_facet Rimmer, Janet
Santos, Conceição
Yli-Panula, Eija
Noronha, Virginia
Viander, Markku
author_sort Rimmer, Janet
collection PubMed
description BACKGROUND: The precise way in which allergen is handled by the nose is unknown. The objective of this study was to determine recovery of Der p 1 allergen following nasal administration and to determine whether Der p 1 can be detected in nasal biopsies after natural exposure and nasal challenge to allergen. METHODS: (1) 20 nonatopic non-rhinitics were challenged with Der p 1 and recovery was measured by ELISA in the nasal wash, nasal mucus and induced sputum up to 30 minutes. Particulate charcoal (<40 μm) served as control. (2) In 8 subjects (5 atopics), 30 to 60 minutes after challenge histological localisation of Der p 1 in the nasal mucosal epithelium, subepithelial mucous glands and lamina propria was performed. Co-localisation of Der p 1 with macrophages and IgE-positive cells was undertaken. RESULTS: (1) Less than 25% of total allergen was retrievable after aqueous or particulate challenge, most from the nasal mucus during 1-5 min after the challenge. The median of carbon particles recovered was 9%. (2) Prechallenge Der p 1 staining was associated with the epithelium and subepithelial mucous glands. After challenge there was a trend for greater Der p 1 deposition in atopics, but both atopics and nonatopics showed increases in the number of Der p 1 stained cells and stained tissue compartments. In atopics, increased eosinophils, macrophages and IgE positive cells co-localized with Der p 1 staining. CONCLUSIONS: Der p 1 allergen is detected in nasal tissue independent of atopic status after natural exposure. After challenge the nose effectively retains allergen, which remains mucosally associated; in atopics there is greater Der p 1 deposition and inflammatory response than in nonatopics. These results support the hypothesis that nasal mucus and tissue act as a reservoir for the inhaled Der p 1 allergen leading to a persistent allergic inflammatory response in susceptible individuals.
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spelling pubmed-44305402015-05-21 Clinical and Laboratory Studies of the Fate of Intranasal Allergen Rimmer, Janet Santos, Conceição Yli-Panula, Eija Noronha, Virginia Viander, Markku PLoS One Research Article BACKGROUND: The precise way in which allergen is handled by the nose is unknown. The objective of this study was to determine recovery of Der p 1 allergen following nasal administration and to determine whether Der p 1 can be detected in nasal biopsies after natural exposure and nasal challenge to allergen. METHODS: (1) 20 nonatopic non-rhinitics were challenged with Der p 1 and recovery was measured by ELISA in the nasal wash, nasal mucus and induced sputum up to 30 minutes. Particulate charcoal (<40 μm) served as control. (2) In 8 subjects (5 atopics), 30 to 60 minutes after challenge histological localisation of Der p 1 in the nasal mucosal epithelium, subepithelial mucous glands and lamina propria was performed. Co-localisation of Der p 1 with macrophages and IgE-positive cells was undertaken. RESULTS: (1) Less than 25% of total allergen was retrievable after aqueous or particulate challenge, most from the nasal mucus during 1-5 min after the challenge. The median of carbon particles recovered was 9%. (2) Prechallenge Der p 1 staining was associated with the epithelium and subepithelial mucous glands. After challenge there was a trend for greater Der p 1 deposition in atopics, but both atopics and nonatopics showed increases in the number of Der p 1 stained cells and stained tissue compartments. In atopics, increased eosinophils, macrophages and IgE positive cells co-localized with Der p 1 staining. CONCLUSIONS: Der p 1 allergen is detected in nasal tissue independent of atopic status after natural exposure. After challenge the nose effectively retains allergen, which remains mucosally associated; in atopics there is greater Der p 1 deposition and inflammatory response than in nonatopics. These results support the hypothesis that nasal mucus and tissue act as a reservoir for the inhaled Der p 1 allergen leading to a persistent allergic inflammatory response in susceptible individuals. Public Library of Science 2015-05-13 /pmc/articles/PMC4430540/ /pubmed/25969994 http://dx.doi.org/10.1371/journal.pone.0127477 Text en © 2015 Rimmer et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rimmer, Janet
Santos, Conceição
Yli-Panula, Eija
Noronha, Virginia
Viander, Markku
Clinical and Laboratory Studies of the Fate of Intranasal Allergen
title Clinical and Laboratory Studies of the Fate of Intranasal Allergen
title_full Clinical and Laboratory Studies of the Fate of Intranasal Allergen
title_fullStr Clinical and Laboratory Studies of the Fate of Intranasal Allergen
title_full_unstemmed Clinical and Laboratory Studies of the Fate of Intranasal Allergen
title_short Clinical and Laboratory Studies of the Fate of Intranasal Allergen
title_sort clinical and laboratory studies of the fate of intranasal allergen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430540/
https://www.ncbi.nlm.nih.gov/pubmed/25969994
http://dx.doi.org/10.1371/journal.pone.0127477
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