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Inborn Errors of the Immune System Associated With Atopy

Atopic disorders, including atopic dermatitis, food and environmental allergies, and asthma, are increasingly prevalent diseases. Atopic disorders are often associated with eosinophilia, driven by T helper type 2 (Th2) immune responses, and triggered by disrupted barrier function leading to abnormal...

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Detalles Bibliográficos
Autores principales: Nelson, Ryan W., Geha, Raif S., McDonald, Douglas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094424/
https://www.ncbi.nlm.nih.gov/pubmed/35572516
http://dx.doi.org/10.3389/fimmu.2022.860821
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author Nelson, Ryan W.
Geha, Raif S.
McDonald, Douglas R.
author_facet Nelson, Ryan W.
Geha, Raif S.
McDonald, Douglas R.
author_sort Nelson, Ryan W.
collection PubMed
description Atopic disorders, including atopic dermatitis, food and environmental allergies, and asthma, are increasingly prevalent diseases. Atopic disorders are often associated with eosinophilia, driven by T helper type 2 (Th2) immune responses, and triggered by disrupted barrier function leading to abnormal immune priming in a susceptible host. Immune deficiencies, in contrast, occur with a significantly lower incidence, but are associated with greater morbidity and mortality. A subset of atopic disorders with eosinophilia and elevated IgE are associated with monogenic inborn errors of immunity (IEI). In this review, we discuss current knowledge of IEI that are associated with atopy and the lessons these immunologic disorders provide regarding the fundamental mechanisms that regulate type 2 immunity in humans. We also discuss further mechanistic insights provided by animal models.
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spelling pubmed-90944242022-05-12 Inborn Errors of the Immune System Associated With Atopy Nelson, Ryan W. Geha, Raif S. McDonald, Douglas R. Front Immunol Immunology Atopic disorders, including atopic dermatitis, food and environmental allergies, and asthma, are increasingly prevalent diseases. Atopic disorders are often associated with eosinophilia, driven by T helper type 2 (Th2) immune responses, and triggered by disrupted barrier function leading to abnormal immune priming in a susceptible host. Immune deficiencies, in contrast, occur with a significantly lower incidence, but are associated with greater morbidity and mortality. A subset of atopic disorders with eosinophilia and elevated IgE are associated with monogenic inborn errors of immunity (IEI). In this review, we discuss current knowledge of IEI that are associated with atopy and the lessons these immunologic disorders provide regarding the fundamental mechanisms that regulate type 2 immunity in humans. We also discuss further mechanistic insights provided by animal models. Frontiers Media S.A. 2022-04-27 /pmc/articles/PMC9094424/ /pubmed/35572516 http://dx.doi.org/10.3389/fimmu.2022.860821 Text en Copyright © 2022 Nelson, Geha and McDonald https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Nelson, Ryan W.
Geha, Raif S.
McDonald, Douglas R.
Inborn Errors of the Immune System Associated With Atopy
title Inborn Errors of the Immune System Associated With Atopy
title_full Inborn Errors of the Immune System Associated With Atopy
title_fullStr Inborn Errors of the Immune System Associated With Atopy
title_full_unstemmed Inborn Errors of the Immune System Associated With Atopy
title_short Inborn Errors of the Immune System Associated With Atopy
title_sort inborn errors of the immune system associated with atopy
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094424/
https://www.ncbi.nlm.nih.gov/pubmed/35572516
http://dx.doi.org/10.3389/fimmu.2022.860821
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