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The hygiene hypothesis: immunological mechanisms of airway tolerance

The hygiene hypothesis was initially proposed as an explanation for the alarming rise in allergy prevalence in the last century. The immunological idea behind this hypothesis was a lack of infections associated with a Western lifestyle and a consequential reduction in type 1 immune responses. It is...

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Autores principales: Haspeslagh, Eline, Heyndrickx, Ines, Hammad, Hamida, Lambrecht, Bart N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202673/
https://www.ncbi.nlm.nih.gov/pubmed/29986301
http://dx.doi.org/10.1016/j.coi.2018.06.007
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author Haspeslagh, Eline
Heyndrickx, Ines
Hammad, Hamida
Lambrecht, Bart N
author_facet Haspeslagh, Eline
Heyndrickx, Ines
Hammad, Hamida
Lambrecht, Bart N
author_sort Haspeslagh, Eline
collection PubMed
description The hygiene hypothesis was initially proposed as an explanation for the alarming rise in allergy prevalence in the last century. The immunological idea behind this hypothesis was a lack of infections associated with a Western lifestyle and a consequential reduction in type 1 immune responses. It is now understood that the development of tolerance to allergens depends on microbial colonization and immunostimulatory environmental signals during early-life or passed on by the mother. These environmental cues are sensed and integrated by barrier epithelial cells of the lungs and possibly skin, which in turn instruct dendritic cells to regulate or impede adaptive T cell responses. Recent reports also implicate immunoregulatory macrophages as powerful suppressors of allergy by the microbiome. We propose that loss of adequate microbial stimulation due to a Western lifestyle may result in hypersensitive barrier tissues and the observed rise in type 2 allergic disease.
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spelling pubmed-62026732018-10-30 The hygiene hypothesis: immunological mechanisms of airway tolerance Haspeslagh, Eline Heyndrickx, Ines Hammad, Hamida Lambrecht, Bart N Curr Opin Immunol Article The hygiene hypothesis was initially proposed as an explanation for the alarming rise in allergy prevalence in the last century. The immunological idea behind this hypothesis was a lack of infections associated with a Western lifestyle and a consequential reduction in type 1 immune responses. It is now understood that the development of tolerance to allergens depends on microbial colonization and immunostimulatory environmental signals during early-life or passed on by the mother. These environmental cues are sensed and integrated by barrier epithelial cells of the lungs and possibly skin, which in turn instruct dendritic cells to regulate or impede adaptive T cell responses. Recent reports also implicate immunoregulatory macrophages as powerful suppressors of allergy by the microbiome. We propose that loss of adequate microbial stimulation due to a Western lifestyle may result in hypersensitive barrier tissues and the observed rise in type 2 allergic disease. Elsevier 2018-10 /pmc/articles/PMC6202673/ /pubmed/29986301 http://dx.doi.org/10.1016/j.coi.2018.06.007 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Haspeslagh, Eline
Heyndrickx, Ines
Hammad, Hamida
Lambrecht, Bart N
The hygiene hypothesis: immunological mechanisms of airway tolerance
title The hygiene hypothesis: immunological mechanisms of airway tolerance
title_full The hygiene hypothesis: immunological mechanisms of airway tolerance
title_fullStr The hygiene hypothesis: immunological mechanisms of airway tolerance
title_full_unstemmed The hygiene hypothesis: immunological mechanisms of airway tolerance
title_short The hygiene hypothesis: immunological mechanisms of airway tolerance
title_sort hygiene hypothesis: immunological mechanisms of airway tolerance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202673/
https://www.ncbi.nlm.nih.gov/pubmed/29986301
http://dx.doi.org/10.1016/j.coi.2018.06.007
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