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House dust mites as potential carriers for IgE sensitization to bacterial antigens

BACKGROUND: IgE reactivity to antigens from Gram‐positive and Gram‐negative bacteria is common in patients suffering from respiratory and skin manifestations of allergy, but the routes and mechanisms of sensitization are not fully understood. The analysis of the genome, transcriptome and microbiome...

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Autores principales: Dzoro, S., Mittermann, I., Resch‐Marat, Y., Vrtala, S., Nehr, M., Hirschl, A. M., Wikberg, G., Lundeberg, L., Johansson, C., Scheynius, A., Valenta, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763376/
https://www.ncbi.nlm.nih.gov/pubmed/28741705
http://dx.doi.org/10.1111/all.13260
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author Dzoro, S.
Mittermann, I.
Resch‐Marat, Y.
Vrtala, S.
Nehr, M.
Hirschl, A. M.
Wikberg, G.
Lundeberg, L.
Johansson, C.
Scheynius, A.
Valenta, R.
author_facet Dzoro, S.
Mittermann, I.
Resch‐Marat, Y.
Vrtala, S.
Nehr, M.
Hirschl, A. M.
Wikberg, G.
Lundeberg, L.
Johansson, C.
Scheynius, A.
Valenta, R.
author_sort Dzoro, S.
collection PubMed
description BACKGROUND: IgE reactivity to antigens from Gram‐positive and Gram‐negative bacteria is common in patients suffering from respiratory and skin manifestations of allergy, but the routes and mechanisms of sensitization are not fully understood. The analysis of the genome, transcriptome and microbiome of house dust mites (HDM) has shown that Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) species are abundant bacteria within the HDM microbiome. Therefore, our aim was to investigate whether HDM are carriers of bacterial antigens leading to IgE sensitization in patients suffering from atopic dermatitis. METHODS: Plasma samples from patients with AD (n = 179) were analysed for IgE reactivity to a comprehensive panel of microarrayed HDM allergen molecules and to S. aureus and E. coli by IgE immunoblotting. Antibodies specific for S. aureus and E. coli antigens were tested for reactivity to nitrocellulose‐blotted extract from purified HDM bodies, and the IgE‐reactive antigens were detected by IgE immunoblot inhibition experiments. IgE antibodies directed to bacterial antigens in HDM were quantified by IgE ImmunoCAP™ inhibition experiments. RESULTS: IgE reactivity to bacterial antigens was significantly more frequent in patients with AD sensitized to HDM than in AD patients without HDM sensitization. S. aureus and E. coli antigens were detected in immune‐blotted HDM extract, and the presence of IgE‐reactive antigens in HDM was demonstrated by qualitative and quantitative IgE inhibition experiments. CONCLUSION: House dust mites (HDM) may serve as carriers of bacteria responsible for the induction of IgE sensitization to microbial antigens.
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spelling pubmed-57633762018-01-17 House dust mites as potential carriers for IgE sensitization to bacterial antigens Dzoro, S. Mittermann, I. Resch‐Marat, Y. Vrtala, S. Nehr, M. Hirschl, A. M. Wikberg, G. Lundeberg, L. Johansson, C. Scheynius, A. Valenta, R. Allergy ORIGINAL ARTICLES BACKGROUND: IgE reactivity to antigens from Gram‐positive and Gram‐negative bacteria is common in patients suffering from respiratory and skin manifestations of allergy, but the routes and mechanisms of sensitization are not fully understood. The analysis of the genome, transcriptome and microbiome of house dust mites (HDM) has shown that Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) species are abundant bacteria within the HDM microbiome. Therefore, our aim was to investigate whether HDM are carriers of bacterial antigens leading to IgE sensitization in patients suffering from atopic dermatitis. METHODS: Plasma samples from patients with AD (n = 179) were analysed for IgE reactivity to a comprehensive panel of microarrayed HDM allergen molecules and to S. aureus and E. coli by IgE immunoblotting. Antibodies specific for S. aureus and E. coli antigens were tested for reactivity to nitrocellulose‐blotted extract from purified HDM bodies, and the IgE‐reactive antigens were detected by IgE immunoblot inhibition experiments. IgE antibodies directed to bacterial antigens in HDM were quantified by IgE ImmunoCAP™ inhibition experiments. RESULTS: IgE reactivity to bacterial antigens was significantly more frequent in patients with AD sensitized to HDM than in AD patients without HDM sensitization. S. aureus and E. coli antigens were detected in immune‐blotted HDM extract, and the presence of IgE‐reactive antigens in HDM was demonstrated by qualitative and quantitative IgE inhibition experiments. CONCLUSION: House dust mites (HDM) may serve as carriers of bacteria responsible for the induction of IgE sensitization to microbial antigens. John Wiley and Sons Inc. 2017-09-07 2018-01 /pmc/articles/PMC5763376/ /pubmed/28741705 http://dx.doi.org/10.1111/all.13260 Text en © 2017 The Authors. Allergy Published by John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle ORIGINAL ARTICLES
Dzoro, S.
Mittermann, I.
Resch‐Marat, Y.
Vrtala, S.
Nehr, M.
Hirschl, A. M.
Wikberg, G.
Lundeberg, L.
Johansson, C.
Scheynius, A.
Valenta, R.
House dust mites as potential carriers for IgE sensitization to bacterial antigens
title House dust mites as potential carriers for IgE sensitization to bacterial antigens
title_full House dust mites as potential carriers for IgE sensitization to bacterial antigens
title_fullStr House dust mites as potential carriers for IgE sensitization to bacterial antigens
title_full_unstemmed House dust mites as potential carriers for IgE sensitization to bacterial antigens
title_short House dust mites as potential carriers for IgE sensitization to bacterial antigens
title_sort house dust mites as potential carriers for ige sensitization to bacterial antigens
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763376/
https://www.ncbi.nlm.nih.gov/pubmed/28741705
http://dx.doi.org/10.1111/all.13260
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