Lower FOXP3 mRNA Expression in First-Trimester Decidual Tissue from Uncomplicated Term Pregnancies with a Male Fetus

Pregnancies with a male fetus are associated with higher risks of pregnancy complications through maladaptation of the maternal immune system. The pathophysiology of this phenomenon is unknown. A possible pathway could be a fetal sex-dependent maternal immune response, since males have a Y chromosom...

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Main Authors: Tom E. C. Kieffer, Anne Laskewitz, Marijke M. Faas, Sicco A. Scherjon, Jan Jaap H. M. Erwich, Sanne J. Gordijn, Jelmer R. Prins
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2018/1950879
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author Tom E. C. Kieffer
Anne Laskewitz
Marijke M. Faas
Sicco A. Scherjon
Jan Jaap H. M. Erwich
Sanne J. Gordijn
Jelmer R. Prins
author_facet Tom E. C. Kieffer
Anne Laskewitz
Marijke M. Faas
Sicco A. Scherjon
Jan Jaap H. M. Erwich
Sanne J. Gordijn
Jelmer R. Prins
author_sort Tom E. C. Kieffer
collection DOAJ
description Pregnancies with a male fetus are associated with higher risks of pregnancy complications through maladaptation of the maternal immune system. The pathophysiology of this phenomenon is unknown. A possible pathway could be a fetal sex-dependent maternal immune response, since males have a Y chromosome encoding specific allogenic proteins, possibly contributing to a different response and higher complication risks. To analyze whether fetal sex affects mRNA expression of maternal immune genes in early pregnancy, real-time PCR quantification was performed in the decidual tissue from primigravid pregnancies (n=20) between 10 and 12 weeks with uncomplicated term outcomes. Early-pregnancy decidual mRNA expression of the regulatory T-cell marker, FOXP3, was sixfold lower (p<0.01) in pregnancies with a male fetus compared to pregnancies with a female fetus. Additionally, mRNA expression of IFNγ was sixfold (p<0.05) lower in pregnancies with a male fetus. The present data imply maternal immunologic differences between pregnancies with male and female fetuses which could be involved in different pregnancy pathophysiologic outcomes. Moreover, this study indicates that researchers in reproductive immunology should always consider fetal sex bias.
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publishDate 2018-01-01
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series Journal of Immunology Research
spelling doaj-art-4f5e225651e3414e9d97a6167158f9902025-02-03T05:58:11ZengWileyJournal of Immunology Research2314-88612314-71562018-01-01201810.1155/2018/19508791950879Lower FOXP3 mRNA Expression in First-Trimester Decidual Tissue from Uncomplicated Term Pregnancies with a Male FetusTom E. C. Kieffer0Anne Laskewitz1Marijke M. Faas2Sicco A. Scherjon3Jan Jaap H. M. Erwich4Sanne J. Gordijn5Jelmer R. Prins6Department of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, P.O. Box 30001, 9700 RB Groningen, NetherlandsDepartment of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, P.O. Box 30001, 9700 RB Groningen, NetherlandsDepartment of Pathology and Medical Biology, Division of Medical Biology, University Medical Center Groningen, University of Groningen, P.O. Box 30001, 9700 RB Groningen, NetherlandsDepartment of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, P.O. Box 30001, 9700 RB Groningen, NetherlandsDepartment of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, P.O. Box 30001, 9700 RB Groningen, NetherlandsDepartment of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, P.O. Box 30001, 9700 RB Groningen, NetherlandsDepartment of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, P.O. Box 30001, 9700 RB Groningen, NetherlandsPregnancies with a male fetus are associated with higher risks of pregnancy complications through maladaptation of the maternal immune system. The pathophysiology of this phenomenon is unknown. A possible pathway could be a fetal sex-dependent maternal immune response, since males have a Y chromosome encoding specific allogenic proteins, possibly contributing to a different response and higher complication risks. To analyze whether fetal sex affects mRNA expression of maternal immune genes in early pregnancy, real-time PCR quantification was performed in the decidual tissue from primigravid pregnancies (n=20) between 10 and 12 weeks with uncomplicated term outcomes. Early-pregnancy decidual mRNA expression of the regulatory T-cell marker, FOXP3, was sixfold lower (p<0.01) in pregnancies with a male fetus compared to pregnancies with a female fetus. Additionally, mRNA expression of IFNγ was sixfold (p<0.05) lower in pregnancies with a male fetus. The present data imply maternal immunologic differences between pregnancies with male and female fetuses which could be involved in different pregnancy pathophysiologic outcomes. Moreover, this study indicates that researchers in reproductive immunology should always consider fetal sex bias.http://dx.doi.org/10.1155/2018/1950879
spellingShingle Tom E. C. Kieffer
Anne Laskewitz
Marijke M. Faas
Sicco A. Scherjon
Jan Jaap H. M. Erwich
Sanne J. Gordijn
Jelmer R. Prins
Lower FOXP3 mRNA Expression in First-Trimester Decidual Tissue from Uncomplicated Term Pregnancies with a Male Fetus
Journal of Immunology Research
title Lower FOXP3 mRNA Expression in First-Trimester Decidual Tissue from Uncomplicated Term Pregnancies with a Male Fetus
title_full Lower FOXP3 mRNA Expression in First-Trimester Decidual Tissue from Uncomplicated Term Pregnancies with a Male Fetus
title_fullStr Lower FOXP3 mRNA Expression in First-Trimester Decidual Tissue from Uncomplicated Term Pregnancies with a Male Fetus
title_full_unstemmed Lower FOXP3 mRNA Expression in First-Trimester Decidual Tissue from Uncomplicated Term Pregnancies with a Male Fetus
title_short Lower FOXP3 mRNA Expression in First-Trimester Decidual Tissue from Uncomplicated Term Pregnancies with a Male Fetus
title_sort lower foxp3 mrna expression in first trimester decidual tissue from uncomplicated term pregnancies with a male fetus
url http://dx.doi.org/10.1155/2018/1950879
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