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Neonatal Immune State Is Influenced by Maternal Allergic Rhinitis and Associated With Regulatory T cells

PURPOSE: Maternal influences contribute to the origin of allergic diseases, but the mechanisms are not clear. The current literature prompted the role of epigenetics in the development of allergic diseases. We sought to investigate the roles of regulatory T (Treg) cells and Forkhead box p3 (Foxp3) D...

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Autores principales: Tan, Lu, Ou, Jing, Tao, Zezhang, Kong, Yonggang, Xu, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266115/
https://www.ncbi.nlm.nih.gov/pubmed/28102058
http://dx.doi.org/10.4168/aair.2017.9.2.133
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author Tan, Lu
Ou, Jing
Tao, Zezhang
Kong, Yonggang
Xu, Yu
author_facet Tan, Lu
Ou, Jing
Tao, Zezhang
Kong, Yonggang
Xu, Yu
author_sort Tan, Lu
collection PubMed
description PURPOSE: Maternal influences contribute to the origin of allergic diseases, but the mechanisms are not clear. The current literature prompted the role of epigenetics in the development of allergic diseases. We sought to investigate the roles of regulatory T (Treg) cells and Forkhead box p3 (Foxp3) DNA methylation in the process of maternal transmission of allergic rhinitis (AR) susceptibility. METHODS: BALB/c female mice (AR mother) were sensitized by intraperitoneal injection of Dermatophagoides pteronyssinus (Der p) 1 on day 1 and 7. Then they mated with normal male mice on day 8. From day 21 to 28, the female mice were intranasal challenged with Der p 1 continuously. The normal controls were given with normal saline in the same way. On postnatal day 3, Female mice and their offspring were sacrificed to detect their histopathology in nasal mucosae, cytokines in sera of mother and spleen homogenates of offspring, Treg cells count, Foxp3 mRNA expressions, and Foxp3 DNA methylation levels in spleens. RESULTS: Compared with the normal controls, neonatal offspring of Der p 1-stimulated female mice (AR offspring) showed the elevation of interleukin (IL)-4 (P<0.01) and IL-17 (P<0.01), the submission of IL-10 (P<0.01) in spleen homogenates. Further, Treg cells count in AR offspring decreased remarkably compared with the normal offspring (P<0.01). Though the difference of Foxp3 DNA methylation level between AR offspring and normal control offspring was not obvious, correlation analysis demonstrated that there was significantly positive correlation between Foxp3 DNA methylation level of mother and that of offspring (r=0.803, P<0.01). CONCLUSIONS: Under the influence of Maternal AR, their neonatal offspring develop into T-helper type 2 (Th2) dominant immune state, which is closely associated with the recession of Treg cells. Foxp3 DNA methylation may be a mechanism responsible for that maternal effect but still need more studies to ensure.
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spelling pubmed-52661152017-03-01 Neonatal Immune State Is Influenced by Maternal Allergic Rhinitis and Associated With Regulatory T cells Tan, Lu Ou, Jing Tao, Zezhang Kong, Yonggang Xu, Yu Allergy Asthma Immunol Res Original Article PURPOSE: Maternal influences contribute to the origin of allergic diseases, but the mechanisms are not clear. The current literature prompted the role of epigenetics in the development of allergic diseases. We sought to investigate the roles of regulatory T (Treg) cells and Forkhead box p3 (Foxp3) DNA methylation in the process of maternal transmission of allergic rhinitis (AR) susceptibility. METHODS: BALB/c female mice (AR mother) were sensitized by intraperitoneal injection of Dermatophagoides pteronyssinus (Der p) 1 on day 1 and 7. Then they mated with normal male mice on day 8. From day 21 to 28, the female mice were intranasal challenged with Der p 1 continuously. The normal controls were given with normal saline in the same way. On postnatal day 3, Female mice and their offspring were sacrificed to detect their histopathology in nasal mucosae, cytokines in sera of mother and spleen homogenates of offspring, Treg cells count, Foxp3 mRNA expressions, and Foxp3 DNA methylation levels in spleens. RESULTS: Compared with the normal controls, neonatal offspring of Der p 1-stimulated female mice (AR offspring) showed the elevation of interleukin (IL)-4 (P<0.01) and IL-17 (P<0.01), the submission of IL-10 (P<0.01) in spleen homogenates. Further, Treg cells count in AR offspring decreased remarkably compared with the normal offspring (P<0.01). Though the difference of Foxp3 DNA methylation level between AR offspring and normal control offspring was not obvious, correlation analysis demonstrated that there was significantly positive correlation between Foxp3 DNA methylation level of mother and that of offspring (r=0.803, P<0.01). CONCLUSIONS: Under the influence of Maternal AR, their neonatal offspring develop into T-helper type 2 (Th2) dominant immune state, which is closely associated with the recession of Treg cells. Foxp3 DNA methylation may be a mechanism responsible for that maternal effect but still need more studies to ensure. The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2017-03 2016-11-23 /pmc/articles/PMC5266115/ /pubmed/28102058 http://dx.doi.org/10.4168/aair.2017.9.2.133 Text en Copyright © 2017 The Korean Academy of Asthma, Allergy and Clinical Immunology • The Korean Academy of Pediatric Allergy and Respiratory Disease http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tan, Lu
Ou, Jing
Tao, Zezhang
Kong, Yonggang
Xu, Yu
Neonatal Immune State Is Influenced by Maternal Allergic Rhinitis and Associated With Regulatory T cells
title Neonatal Immune State Is Influenced by Maternal Allergic Rhinitis and Associated With Regulatory T cells
title_full Neonatal Immune State Is Influenced by Maternal Allergic Rhinitis and Associated With Regulatory T cells
title_fullStr Neonatal Immune State Is Influenced by Maternal Allergic Rhinitis and Associated With Regulatory T cells
title_full_unstemmed Neonatal Immune State Is Influenced by Maternal Allergic Rhinitis and Associated With Regulatory T cells
title_short Neonatal Immune State Is Influenced by Maternal Allergic Rhinitis and Associated With Regulatory T cells
title_sort neonatal immune state is influenced by maternal allergic rhinitis and associated with regulatory t cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266115/
https://www.ncbi.nlm.nih.gov/pubmed/28102058
http://dx.doi.org/10.4168/aair.2017.9.2.133
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