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Federal government websites often end in. The site is secure. Preview improvements coming to the PMC website in October Learn More or Try it out now. All data generated or analyzed during this study are included in this published article and its supplementary information files or from the corresponding author upon reasonable request. The source data underlying Figs. Maternal immune dysregulation seems to affect fetal or postnatal immune development. Preeclampsia is a pregnancy-associated disorder with an immune basis and is linked to atopic disorders in offspring.
Here we show reduction of fetal thymic size, altered thymic architecture and reduced fetal thymic regulatory T Treg cell output in preeclamptic pregnancies, which persists up to 4 years of age in human offspring.
In our human cohorts, low maternal serum acetate is associated with subsequent preeclampsia, and correlates with serum acetate in the fetus. These findings suggest a potential role of acetate in the pathogenesis of preeclampsia and immune development in offspring. Maternal immunological dysregulation might affect the immunological development of the fetus. Here the authors show that decreased maternal acetate is associated with preeclampsia, impaired fetal thymic output and regulatory T cell development.
The maternal and early in utero environment probably affects health and disease later in life. This is particularly true of non-communicable diseases such as allergy and autoimmunity 1. Preeclampsia is a common pregnancy-associated disorder that is unique to humans.