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Sex Steroids Effects on Asthma: A Network Perspective of Immune and Airway Cells

A multitude of evidence has suggested the differential incidence, prevalence and severity of asthma between males and females. A compilation of recent literature recognized sex differences as a significant non-modifiable risk factor in asthma pathogenesis. Understanding the cellular and mechanistic...

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Autores principales: Borkar, Niyati A., Combs, Colin Kelly, Sathish, Venkatachalem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318292/
https://www.ncbi.nlm.nih.gov/pubmed/35883681
http://dx.doi.org/10.3390/cells11142238
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author Borkar, Niyati A.
Combs, Colin Kelly
Sathish, Venkatachalem
author_facet Borkar, Niyati A.
Combs, Colin Kelly
Sathish, Venkatachalem
author_sort Borkar, Niyati A.
collection PubMed
description A multitude of evidence has suggested the differential incidence, prevalence and severity of asthma between males and females. A compilation of recent literature recognized sex differences as a significant non-modifiable risk factor in asthma pathogenesis. Understanding the cellular and mechanistic basis of sex differences remains complex and the pivotal point of this ever elusive quest, which remains to be clarified in the current scenario. Sex steroids are an integral part of human development and evolution while also playing a critical role in the conditioning of the immune system and thereby influencing the function of peripheral organs. Classical perspectives suggest a pre-defined effect of sex steroids, generalizing estrogens popularly under the “estrogen paradox” due to conflicting reports associating estrogen with a pro- and anti-inflammatory role. On the other hand, androgens are classified as “anti-inflammatory,” serving a protective role in mitigating inflammation. Although considered mainstream and simplistic, this observation remains valid for numerous reasons, as elaborated in the current review. Women appear immune-favored with stronger and more responsive immune elements than men. However, the remarkable female predominance of diverse autoimmune and allergic diseases contradicts this observation suggesting that hormonal differences between the sexes might modulate the normal and dysfunctional regulation of the immune system. This review illustrates the potential relationship between key elements of the immune cell system and their interplay with sex steroids, relevant to structural cells in the pathophysiology of asthma and many other lung diseases. Here, we discuss established and emerging paradigms in the clarification of observed sex differences in asthma in the context of the immune system, which will deepen our understanding of asthma etiopathology.
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spelling pubmed-93182922022-07-27 Sex Steroids Effects on Asthma: A Network Perspective of Immune and Airway Cells Borkar, Niyati A. Combs, Colin Kelly Sathish, Venkatachalem Cells Review A multitude of evidence has suggested the differential incidence, prevalence and severity of asthma between males and females. A compilation of recent literature recognized sex differences as a significant non-modifiable risk factor in asthma pathogenesis. Understanding the cellular and mechanistic basis of sex differences remains complex and the pivotal point of this ever elusive quest, which remains to be clarified in the current scenario. Sex steroids are an integral part of human development and evolution while also playing a critical role in the conditioning of the immune system and thereby influencing the function of peripheral organs. Classical perspectives suggest a pre-defined effect of sex steroids, generalizing estrogens popularly under the “estrogen paradox” due to conflicting reports associating estrogen with a pro- and anti-inflammatory role. On the other hand, androgens are classified as “anti-inflammatory,” serving a protective role in mitigating inflammation. Although considered mainstream and simplistic, this observation remains valid for numerous reasons, as elaborated in the current review. Women appear immune-favored with stronger and more responsive immune elements than men. However, the remarkable female predominance of diverse autoimmune and allergic diseases contradicts this observation suggesting that hormonal differences between the sexes might modulate the normal and dysfunctional regulation of the immune system. This review illustrates the potential relationship between key elements of the immune cell system and their interplay with sex steroids, relevant to structural cells in the pathophysiology of asthma and many other lung diseases. Here, we discuss established and emerging paradigms in the clarification of observed sex differences in asthma in the context of the immune system, which will deepen our understanding of asthma etiopathology. MDPI 2022-07-19 /pmc/articles/PMC9318292/ /pubmed/35883681 http://dx.doi.org/10.3390/cells11142238 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Borkar, Niyati A.
Combs, Colin Kelly
Sathish, Venkatachalem
Sex Steroids Effects on Asthma: A Network Perspective of Immune and Airway Cells
title Sex Steroids Effects on Asthma: A Network Perspective of Immune and Airway Cells
title_full Sex Steroids Effects on Asthma: A Network Perspective of Immune and Airway Cells
title_fullStr Sex Steroids Effects on Asthma: A Network Perspective of Immune and Airway Cells
title_full_unstemmed Sex Steroids Effects on Asthma: A Network Perspective of Immune and Airway Cells
title_short Sex Steroids Effects on Asthma: A Network Perspective of Immune and Airway Cells
title_sort sex steroids effects on asthma: a network perspective of immune and airway cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318292/
https://www.ncbi.nlm.nih.gov/pubmed/35883681
http://dx.doi.org/10.3390/cells11142238
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