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Primary atopic disorders

Monogenic disorders have provided fundamental insights into human immunity and the pathogenesis of allergic diseases. The pathways identified as critical in the development of atopy range from focal defects in immune cells and epithelial barrier function to global changes in metabolism. A major goal...

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Detalles Bibliográficos
Autores principales: Lyons, Jonathan J., Milner, Joshua D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881472/
https://www.ncbi.nlm.nih.gov/pubmed/29549114
http://dx.doi.org/10.1084/jem.20172306
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author Lyons, Jonathan J.
Milner, Joshua D.
author_facet Lyons, Jonathan J.
Milner, Joshua D.
author_sort Lyons, Jonathan J.
collection PubMed
description Monogenic disorders have provided fundamental insights into human immunity and the pathogenesis of allergic diseases. The pathways identified as critical in the development of atopy range from focal defects in immune cells and epithelial barrier function to global changes in metabolism. A major goal of studying heritable single-gene disorders that lead to severe clinical allergic diseases is to identify fundamental pathways leading to hypersensitivity that can be targeted to provide novel therapeutic strategies for patients with allergic diseases, syndromic and nonsyndromic alike. Here, we review known single-gene disorders leading to severe allergic phenotypes in humans, discuss how the revealed pathways fit within our current understanding of the atopic diathesis, and propose how some pathways might be targeted for therapeutic benefit.
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spelling pubmed-58814722018-10-02 Primary atopic disorders Lyons, Jonathan J. Milner, Joshua D. J Exp Med Reviews Monogenic disorders have provided fundamental insights into human immunity and the pathogenesis of allergic diseases. The pathways identified as critical in the development of atopy range from focal defects in immune cells and epithelial barrier function to global changes in metabolism. A major goal of studying heritable single-gene disorders that lead to severe clinical allergic diseases is to identify fundamental pathways leading to hypersensitivity that can be targeted to provide novel therapeutic strategies for patients with allergic diseases, syndromic and nonsyndromic alike. Here, we review known single-gene disorders leading to severe allergic phenotypes in humans, discuss how the revealed pathways fit within our current understanding of the atopic diathesis, and propose how some pathways might be targeted for therapeutic benefit. Rockefeller University Press 2018-04-02 /pmc/articles/PMC5881472/ /pubmed/29549114 http://dx.doi.org/10.1084/jem.20172306 Text en This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Reviews
Lyons, Jonathan J.
Milner, Joshua D.
Primary atopic disorders
title Primary atopic disorders
title_full Primary atopic disorders
title_fullStr Primary atopic disorders
title_full_unstemmed Primary atopic disorders
title_short Primary atopic disorders
title_sort primary atopic disorders
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881472/
https://www.ncbi.nlm.nih.gov/pubmed/29549114
http://dx.doi.org/10.1084/jem.20172306
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