# Impact of previous pregnancy and BMI on cellular and serum immune activity from early to late pregnancy

**Authors:** Grace Mealy, Kiva Brennan, Sarah Louise Killeen, Mark Kilbane, Cara Yelverton, Radka Saldova, David Groeger, Douwe VanSinderen, Paul D. Cotter, Sarah L. Doyle, Fionnuala M. McAuliffe

PMC · DOI: 10.1038/s41598-024-66651-4 · 2024-07-11

## TL;DR

The study shows how immune responses change during pregnancy and how previous pregnancies and BMI affect these changes, which may explain higher risks for first-time mothers.

## Contribution

The study reveals contrasting immune trends in serum and PBMCs during pregnancy and how parity and BMI influence these responses.

## Key findings

- PBMC cytokines decreased while serum cytokines increased during pregnancy.
- Parous women showed reduced PBMC cytokine levels with gestation, while first-time mothers had higher late pregnancy leptin.
- BMI differences were observed in serum markers like C3, IL-17A, and leptin.

## Abstract

Immunological adaptions during pregnancy play a crucial role in healthy fetal development. Aberrant immune modifications however contribute to adverse pregnancy outcomes, which may be driven by maternal factors such as previous pregnancies and BMI. This secondary analysis of the MicrobeMom2 RCT investigates the changes to maternal inflammatory biomarkers derived from serum and stimulated peripheral blood mononuclear cells (PBMCs) during pregnancy, and the effects of previous pregnancies (parity) and BMI on maternal immune responses. Changes in immune and metabolic biomarkers from early (11–15 weeks’ gestation) to late (28–32 weeks’ gestation) pregnancy were compared using paired t-tests. Participants were then split by parity (nulliparous, parous) and BMI (BMI < 25, BMI > = 25), and the relationship between parity and BMI with immune biomarker levels was examined using independent t-tests, paired t-tests, ANCOVA, and linear regression. Equivalent non-parametric tests were used for skewed data. Recruited women (n = 72) were on average 31.17 (SD ± 4.53) years of age and 25.11 (SD ± 3.82) BMI (kg/m2). Of these, 51 (70.8%) had a previous term pregnancy. Throughout gestation, PBMC cytokines displayed contrasting trends to serum, with a dampening of immune responses noted in PBMCs, and enhanced production of cytokines observed in the serum. Significant decreases in PBMC derived TNF-α, IL-10 and IFN-γ were seen from early to late pregnancy. Serum C3, IL-17A, IL-6, TNF-α, CD163, GDF-15 and leptin increased throughout gestation. First pregnancy was associated with higher levels of leptin in late pregnancy, while parous women showed significant decreases in PBMC derived TNF-α, IL10, and IFN-γ with gestation. Differences in levels of C3, IL-17A, TNF-α, GDF-15 and leptin were observed across BMI groups. Overall, serum-derived cytokines exhibit contrasting levels to those derived from stimulated PBMCs. Maternal immune responses undergo significant changes from early to late pregnancy, which are influenced by parity and BMI. These differences aid our understanding as to why first-time mothers are at greater risk of placental disease such as pre-eclampsia and fetal growth restriction.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL10 (interleukin 10), IFNG (interferon gamma), C3 (complement C3), IL17A (interleukin 17A), IL6 (interleukin 6), CD163 (CD163 molecule), GDF15 (growth differentiation factor 15), lepa (leptin a)
- **Diseases:** pre-eclampsia (MONDO:0005081), fetal growth restriction (MONDO:0005030)

## Full-text entities

- **Genes:** CD163 (CD163 molecule) [NCBI Gene 9332] {aka M130, MM130, SCARI1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, GDF15 (growth differentiation factor 15) [NCBI Gene 9518] {aka GDF-15, HG, MIC-1, MIC1, NAG-1, PDF}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}
- **Diseases:** fetal growth restriction (MESH:D005317), placental disease (MESH:D010922), inflammatory (MESH:D007249), pre-eclampsia (MESH:D011225)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11239859/full.md

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Source: https://tomesphere.com/paper/PMC11239859