Cytokine mapping of sera from women with preeclampsia and normal pregnancies

J Reprod Immunol. 2006 Jun;70(1-2):83-91. doi: 10.1016/j.jri.2005.10.007. Epub 2006 Jan 18.

Abstract

Introduction: Preeclampsia is a pregnancy-specific syndrome. The immune system in preeclampsia is changed with an increased innate activity and there is a hypothesis of a shift towards Th1-type immunity. The aim of this study was to determine a spectrum of soluble immunological factors denoting different aspects of immune activation in third trimester sera from women with preeclampsia (N=15) and compare with levels in sera from normal pregnant women (N=15).

Material and methods: IL-1beta, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12 p40, IL-13, IL-15, IL-17, IFN-alpha, IFN-gamma, TNF-alpha, GM-CSF, MIP-lalpha, MIP-1beta, MCP-1, eotaxin and RANTES were measured in serum using multiplex bead arrays. The levels of soluble CD14 and soluble IL-4 receptor were measured by enzyme-linked immunoassay (ELISA).

Results: Preeclamptic women had significantly increased levels of circulating IL-6 (p=0.002), IL-8 (p=0.003) and soluble IL-4R (p=0.037), compared to women with normal pregnancies.

Conclusion: This study supports the hypothesis of increased inflammatory responses in preeclampsia, illustrated by the increased levels of IL-6 and IL-8. The finding of increased levels of soluble IL-4 receptor is an intriguing finding with several interpretations, which may partly support the hypothesis of a Th1 shift in preeclampsia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cytokines / blood*
  • Cytokines / immunology
  • Enzyme-Linked Immunosorbent Assay / methods
  • Female
  • Humans
  • Interleukin-6 / blood
  • Interleukin-6 / immunology
  • Interleukin-8 / blood
  • Interleukin-8 / immunology
  • Pre-Eclampsia / blood*
  • Pre-Eclampsia / immunology
  • Pregnancy / blood*
  • Pregnancy / immunology
  • Receptors, Interleukin-4 / blood
  • Receptors, Interleukin-4 / immunology
  • Th1 Cells / immunology

Substances

  • Cytokines
  • Interleukin-6
  • Interleukin-8
  • Receptors, Interleukin-4