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Preconception allergen sensitization can induce B10 cells in offspring: a potential main role for maternal IgG
BACKGROUND: The mechanisms through which allergies can be inhibited after preconception immunization with allergens are not fully understood. We aimed to evaluate whether maternal immunization can induce a regulatory B (B10) cell population in offspring in concert with allergy inhibition. METHODS: C...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392917/ https://www.ncbi.nlm.nih.gov/pubmed/28428801 http://dx.doi.org/10.1186/s13223-017-0195-8 |
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author | de Oliveira, Marília Garcia Oliveira, Luana de Mendonça Lira, Aline Aparecida de Lima Sgnotto, Fábio da Ressureição Duarte, Alberto José da Silva Sato, Maria Notomi Victor, Jefferson Russo |
author_facet | de Oliveira, Marília Garcia Oliveira, Luana de Mendonça Lira, Aline Aparecida de Lima Sgnotto, Fábio da Ressureição Duarte, Alberto José da Silva Sato, Maria Notomi Victor, Jefferson Russo |
author_sort | de Oliveira, Marília Garcia |
collection | PubMed |
description | BACKGROUND: The mechanisms through which allergies can be inhibited after preconception immunization with allergens are not fully understood. We aimed to evaluate whether maternal immunization can induce a regulatory B (B10) cell population in offspring in concert with allergy inhibition. METHODS: C57BL/6 females were or were not immunized with OVA and were mated with normal WT males. Their offspring were evaluated at 3 days of age or 20 days after neonatal immunization. Human peripheral B cells from atopic and non-atopic individuals were also evaluated. RESULTS: Preconception OVA immunization induced B10 cells in offspring, and IL-10 production appeared to be critical for FcγRIIB upregulation in offspring B cells. Murine and human IL-10-producing B cells responded in vitro to IgG according to the atopic repertoire of the cells. CONCLUSIONS: Our results reveal that maternal immunization induces allergen-specific B10 cells in offspring and a pivotal role for the IgG repertoire in IL-10 production by murine and human B cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13223-017-0195-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5392917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53929172017-04-20 Preconception allergen sensitization can induce B10 cells in offspring: a potential main role for maternal IgG de Oliveira, Marília Garcia Oliveira, Luana de Mendonça Lira, Aline Aparecida de Lima Sgnotto, Fábio da Ressureição Duarte, Alberto José da Silva Sato, Maria Notomi Victor, Jefferson Russo Allergy Asthma Clin Immunol Research BACKGROUND: The mechanisms through which allergies can be inhibited after preconception immunization with allergens are not fully understood. We aimed to evaluate whether maternal immunization can induce a regulatory B (B10) cell population in offspring in concert with allergy inhibition. METHODS: C57BL/6 females were or were not immunized with OVA and were mated with normal WT males. Their offspring were evaluated at 3 days of age or 20 days after neonatal immunization. Human peripheral B cells from atopic and non-atopic individuals were also evaluated. RESULTS: Preconception OVA immunization induced B10 cells in offspring, and IL-10 production appeared to be critical for FcγRIIB upregulation in offspring B cells. Murine and human IL-10-producing B cells responded in vitro to IgG according to the atopic repertoire of the cells. CONCLUSIONS: Our results reveal that maternal immunization induces allergen-specific B10 cells in offspring and a pivotal role for the IgG repertoire in IL-10 production by murine and human B cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13223-017-0195-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-17 /pmc/articles/PMC5392917/ /pubmed/28428801 http://dx.doi.org/10.1186/s13223-017-0195-8 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research de Oliveira, Marília Garcia Oliveira, Luana de Mendonça Lira, Aline Aparecida de Lima Sgnotto, Fábio da Ressureição Duarte, Alberto José da Silva Sato, Maria Notomi Victor, Jefferson Russo Preconception allergen sensitization can induce B10 cells in offspring: a potential main role for maternal IgG |
title | Preconception allergen sensitization can induce B10 cells in offspring: a potential main role for maternal IgG |
title_full | Preconception allergen sensitization can induce B10 cells in offspring: a potential main role for maternal IgG |
title_fullStr | Preconception allergen sensitization can induce B10 cells in offspring: a potential main role for maternal IgG |
title_full_unstemmed | Preconception allergen sensitization can induce B10 cells in offspring: a potential main role for maternal IgG |
title_short | Preconception allergen sensitization can induce B10 cells in offspring: a potential main role for maternal IgG |
title_sort | preconception allergen sensitization can induce b10 cells in offspring: a potential main role for maternal igg |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392917/ https://www.ncbi.nlm.nih.gov/pubmed/28428801 http://dx.doi.org/10.1186/s13223-017-0195-8 |
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