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(1-->3)-beta-D-glucan and endotoxin modulate immune response to inhaled allergen.

Exposure to dust may involve co-exposure to agents which are allergens, together with those which are pro-inflammatory. To study the effects of such a co-exposure, the humoral and inflammatory responses were studied in guinea pigs inhaling the T-cell-dependent antigen ovalbumin (OVA) and the inflamm...

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Detalles Bibliográficos
Autores principales: Rylander, R, Holt, P G
Formato: Texto
Lenguaje:English
Publicado: 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781825/
https://www.ncbi.nlm.nih.gov/pubmed/9836497
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author Rylander, R
Holt, P G
author_facet Rylander, R
Holt, P G
author_sort Rylander, R
collection PubMed
description Exposure to dust may involve co-exposure to agents which are allergens, together with those which are pro-inflammatory. To study the effects of such a co-exposure, the humoral and inflammatory responses were studied in guinea pigs inhaling the T-cell-dependent antigen ovalbumin (OVA) and the inflammatory agents (1 --> 3)-beta-D-glucan and lipopolysaccharide (LPS). The effects were evaluated as inflammatory cells in the lung and serum antibodies to OVA. LPS caused a stimulation of the OVA-induced antibody production which was abolished by simultaneous exposure to (1 --> 3)-beta-D-glucan. An increase of eosinophils after OVA exposure was decreased by co-exposure to (1 --> 3)-beta-D-glucan. The results demonstrate a complex interaction between adaptive and innate immune mechanisms in the lung, determined by exposure to common contaminants in airborne dust.
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spelling pubmed-17818252007-01-25 (1-->3)-beta-D-glucan and endotoxin modulate immune response to inhaled allergen. Rylander, R Holt, P G Mediators Inflamm Research Article Exposure to dust may involve co-exposure to agents which are allergens, together with those which are pro-inflammatory. To study the effects of such a co-exposure, the humoral and inflammatory responses were studied in guinea pigs inhaling the T-cell-dependent antigen ovalbumin (OVA) and the inflammatory agents (1 --> 3)-beta-D-glucan and lipopolysaccharide (LPS). The effects were evaluated as inflammatory cells in the lung and serum antibodies to OVA. LPS caused a stimulation of the OVA-induced antibody production which was abolished by simultaneous exposure to (1 --> 3)-beta-D-glucan. An increase of eosinophils after OVA exposure was decreased by co-exposure to (1 --> 3)-beta-D-glucan. The results demonstrate a complex interaction between adaptive and innate immune mechanisms in the lung, determined by exposure to common contaminants in airborne dust. 1998 /pmc/articles/PMC1781825/ /pubmed/9836497 Text en
spellingShingle Research Article
Rylander, R
Holt, P G
(1-->3)-beta-D-glucan and endotoxin modulate immune response to inhaled allergen.
title (1-->3)-beta-D-glucan and endotoxin modulate immune response to inhaled allergen.
title_full (1-->3)-beta-D-glucan and endotoxin modulate immune response to inhaled allergen.
title_fullStr (1-->3)-beta-D-glucan and endotoxin modulate immune response to inhaled allergen.
title_full_unstemmed (1-->3)-beta-D-glucan and endotoxin modulate immune response to inhaled allergen.
title_short (1-->3)-beta-D-glucan and endotoxin modulate immune response to inhaled allergen.
title_sort (1-->3)-beta-d-glucan and endotoxin modulate immune response to inhaled allergen.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781825/
https://www.ncbi.nlm.nih.gov/pubmed/9836497
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