Cervical leukocytes and spontaneous preterm birth

J Reprod Immunol. 2016 Feb:113:42-9. doi: 10.1016/j.jri.2015.11.002. Epub 2015 Nov 21.

Abstract

The objective was to characterise cervical leukocyte populations and inflammatory mediators associated with term and recurrent spontaneous preterm birth (SPTB) in pregnant women with a history of SPTB. A prospective observational study was undertaken on 120 women with a history of SPTB. A cytobrush was used to sample cells from the cervix at 12-25 weeks' gestation. Cells were enumerated and characterised by flow cytometry. Cytokines and chemokines were also measured. Participants were then grouped according to delivery at term (>36+6 weeks), late SPTB (34-36+6 weeks) or early SPTB (<34 weeks). Differences in leukocyte sub-populations, cytokine and chemokine levels were compared with outcome. Cervical leukocytes comprised up to 60% of the host-derived cells. Most of these (90-100%) were polymorphonuclear cells (PMN). Most of the remaining cells were mucosal macrophages expressing CD68 and CD103 in addition to markers shared with blood-borne monocytes. Failure to detect cervical macrophages in at least 250,000 cervical epithelial cells was a feature of women who experienced early SPTB (6 out of 6 cases, 95% CI 61-100%) compared with 34% (30 out of 88 cases, 95% CI 25-43%, P<0.001) of women delivering after 34 weeks. CCL2 (MCP-1) was also low in SPTB before 34 weeks and levels above 75 ng/g and/or the presence of macrophages increased the specificity for birth after 34 weeks from 66% to 82% (55 out of 67 cases, 95% CI 73-91%). Absence of cervical macrophages and low CCL2 may be features of pregnancies at risk of early SPTB.

Keywords: Flow cytometry; Leukocyte; Macrophage; Polymorphonuclear cell; Spontaneous preterm birth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / metabolism
  • Cervix Uteri / immunology*
  • Cervix Uteri / metabolism
  • Cervix Uteri / pathology
  • Chemokine CCL2 / immunology*
  • Chemokine CCL2 / metabolism
  • Female
  • Humans
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Macrophages / pathology
  • Pregnancy
  • Pregnancy Trimester, First / immunology
  • Pregnancy Trimester, First / metabolism
  • Pregnancy Trimester, Second / immunology
  • Pregnancy Trimester, Second / metabolism
  • Premature Birth / immunology*
  • Premature Birth / metabolism
  • Premature Birth / pathology
  • Risk Factors

Substances

  • Biomarkers
  • CCL2 protein, human
  • Chemokine CCL2