4.5 Article

Maternal body mass index is associated with an altered immunological profile at 28 weeks of gestation

Journal

CLINICAL AND EXPERIMENTAL IMMUNOLOGY
Volume 208, Issue 1, Pages 114-128

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/cei/uxac023

Keywords

obesity; pregnancy; immunometabolism; cytokines; Th subset

Categories

Funding

  1. Diabetes UK
  2. Welsh Government Ser Cymru

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This paper explores the impact of pre-pregnancy body mass index (BMI) on the immune profile of GDM-negative pregnant women. It finds that maternal obesity creates an inflammatory microenvironment and alters the immune response, which may have negative effects on pregnancy.
This paper describes the effect of pre-pregnancy body mass index (BMI) on the immune profile of peripheral blood from GDM-negative, pregnant women at 28 weeks of gestation. It reveals a phenotype of systemic inflammation, monocyte activation and altered Th1/Th2/Th17 balance Healthy pregnancy is accompanied by various immunological and metabolic adaptations. Maternal obesity has been implicated in adverse pregnancy outcomes such as miscarriage, preeclampsia, and gestational diabetes mellitus (GDM), while posing a risk to the neonate. There is a lack of knowledge surrounding obesity and the maternal immune system. The objective of this study was to consider if immunological changes in pregnancy are influenced by maternal obesity. Peripheral blood was collected from fasted GDM-negative pregnant women at 26-28 weeks of gestation. Analysis was done using immunoassay, flow cytometry, bioenergetics analysis, and cell culture. The plasma profile was significantly altered with increasing BMI, specifically leptin (r = 0.7635), MCP-1 (r = 0.3024), and IL-6 (r = 0.4985). Circulating leukocyte populations were also affected with changes in the relative abundance of intermediate monocytes (r = -0.2394), CD4:CD8 T-cell ratios (r = 0.2789), and NKT cells (r = -0.2842). Monocytes analysed in more detail revealed elevated CCR2 expression and decreased mitochondrial content with increased BMI. However, LPS-stimulated cytokine production and bioenergetic profile of PBMCs were not affected by maternal BMI. The Th profile skews towards Th17 with increasing BMI; Th2 (r = -0.3202) and Th9 (r = -0.3205) cells were diminished in maternal obesity, and CytoStim (TM)-stimulation exacerbates IL-6 (r = 0.4166), IL-17A (r = 0.2753), IL-17F (r = 0.2973), and IL-22 (r = 0.2257) production with BMI, while decreasing IL-4 (r = -0.2806). Maternal obesity during pregnancy creates an inflammatory microenvironment. Successful pregnancy requires Th2-biased responses yet increasing maternal BMI favours a Th17 response that could be detrimental to pregnancy. Further research should investigate key populations of cells identified here to further understand the immunological challenges that beset pregnant women with obesity.

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