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Dihydrotestosterone levels at birth associate positively with higher proportions of circulating immature/naïve CD5(+) B cells in boys

Boys present with higher proportions of immature/naïve CD5(+) B cells than girls up to 3 years of age. Boys also have higher fractions of regulatory T cells (Tregs) in early infancy, but the mechanisms for these sex-related differences are unknown. In the prospective FARMFLORA follow-up study of 23...

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Autores principales: Lundell, Anna-Carin, Nordström, Inger, Andersson, Kerstin, Strömbeck, Anna, Ohlsson, Claes, Tivesten, Åsa, Rudin, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686210/
https://www.ncbi.nlm.nih.gov/pubmed/29138503
http://dx.doi.org/10.1038/s41598-017-15836-1
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author Lundell, Anna-Carin
Nordström, Inger
Andersson, Kerstin
Strömbeck, Anna
Ohlsson, Claes
Tivesten, Åsa
Rudin, Anna
author_facet Lundell, Anna-Carin
Nordström, Inger
Andersson, Kerstin
Strömbeck, Anna
Ohlsson, Claes
Tivesten, Åsa
Rudin, Anna
author_sort Lundell, Anna-Carin
collection PubMed
description Boys present with higher proportions of immature/naïve CD5(+) B cells than girls up to 3 years of age. Boys also have higher fractions of regulatory T cells (Tregs) in early infancy, but the mechanisms for these sex-related differences are unknown. In the prospective FARMFLORA follow-up study of 23 boys and 25 girls, we investigated if these immunological differences remained at 8 years of age. We also examined if testosterone or dihydrotestosterone (DHT) levels at birth and at 8 years of age were associated with immune maturation. Immunological variables and androgen levels were examined and measured in blood samples obtained at birth, 3–5 days and at 8 years of age. Boys had higher proportions of CD5(+) and immature/transitional CD24(hi)CD38(hi) B cells, whereas girls had higher fractions of B cells with a memory phenotype at 8 years of age. School-aged boys also presented with higher frequencies of Tregs, and a greater capacity to produce T-cell-associated cytokines. Among boys, higher cord blood DHT levels were associated with higher proportions of CD5(+) B cells in early infancy and at 8 years of life. These results suggest that DHT actions in utero might be involved in the mechanism for delayed peripheral B-cell maturation in boys.
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spelling pubmed-56862102017-11-21 Dihydrotestosterone levels at birth associate positively with higher proportions of circulating immature/naïve CD5(+) B cells in boys Lundell, Anna-Carin Nordström, Inger Andersson, Kerstin Strömbeck, Anna Ohlsson, Claes Tivesten, Åsa Rudin, Anna Sci Rep Article Boys present with higher proportions of immature/naïve CD5(+) B cells than girls up to 3 years of age. Boys also have higher fractions of regulatory T cells (Tregs) in early infancy, but the mechanisms for these sex-related differences are unknown. In the prospective FARMFLORA follow-up study of 23 boys and 25 girls, we investigated if these immunological differences remained at 8 years of age. We also examined if testosterone or dihydrotestosterone (DHT) levels at birth and at 8 years of age were associated with immune maturation. Immunological variables and androgen levels were examined and measured in blood samples obtained at birth, 3–5 days and at 8 years of age. Boys had higher proportions of CD5(+) and immature/transitional CD24(hi)CD38(hi) B cells, whereas girls had higher fractions of B cells with a memory phenotype at 8 years of age. School-aged boys also presented with higher frequencies of Tregs, and a greater capacity to produce T-cell-associated cytokines. Among boys, higher cord blood DHT levels were associated with higher proportions of CD5(+) B cells in early infancy and at 8 years of life. These results suggest that DHT actions in utero might be involved in the mechanism for delayed peripheral B-cell maturation in boys. Nature Publishing Group UK 2017-11-14 /pmc/articles/PMC5686210/ /pubmed/29138503 http://dx.doi.org/10.1038/s41598-017-15836-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lundell, Anna-Carin
Nordström, Inger
Andersson, Kerstin
Strömbeck, Anna
Ohlsson, Claes
Tivesten, Åsa
Rudin, Anna
Dihydrotestosterone levels at birth associate positively with higher proportions of circulating immature/naïve CD5(+) B cells in boys
title Dihydrotestosterone levels at birth associate positively with higher proportions of circulating immature/naïve CD5(+) B cells in boys
title_full Dihydrotestosterone levels at birth associate positively with higher proportions of circulating immature/naïve CD5(+) B cells in boys
title_fullStr Dihydrotestosterone levels at birth associate positively with higher proportions of circulating immature/naïve CD5(+) B cells in boys
title_full_unstemmed Dihydrotestosterone levels at birth associate positively with higher proportions of circulating immature/naïve CD5(+) B cells in boys
title_short Dihydrotestosterone levels at birth associate positively with higher proportions of circulating immature/naïve CD5(+) B cells in boys
title_sort dihydrotestosterone levels at birth associate positively with higher proportions of circulating immature/naïve cd5(+) b cells in boys
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686210/
https://www.ncbi.nlm.nih.gov/pubmed/29138503
http://dx.doi.org/10.1038/s41598-017-15836-1
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