Spontaneous labor onset: is it immunologically mediated?

Am J Obstet Gynecol. 2010 Mar;202(3):268.e1-7. doi: 10.1016/j.ajog.2009.10.875. Epub 2010 Jan 1.

Abstract

Objective: The investigators tested the hypothesis that maternal-fetal immune interactions could be important in initiating spontaneous labor onset by examining if labor was delayed when fetuses share maternal HLA antigen types.

Study design: HLA antigen types A, B, and DR in 200 Danish mother-infant pairs delivering in 42-44 weeks (postterm) were compared with 195 mother-infant pairs delivering in 37-40 weeks (term).

Results: Sharing of HLA A and B antigens was more common than expected in postterm deliveries. Odds ratios were 1.54 (95% confidence interval [CI], 1.01-2.35) and 1.75 (95% CI, 0.87-3.52), respectively (risk per shared antigen: 1.40 [95% CI, 1.04-1.90] per unit increase). Adding stringent birth-length criteria for postmaturity (92 cases; 168 controls) strengthened risks associated with antigen sharing to 1.57 (95% CI, 0.90-2.74) and 2.60 (95% CI, 1.15-5.88), respectively (risk per shared antigen: 1.60 (95% CI, 1.10-2.32).

Conclusion: Postterm-delivered infants had more HLA A and B antigens in common with their mothers, suggesting that recognition of HLA antigen differences by adaptive immunity may have a role in triggering labor onset.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Body Height
  • Case-Control Studies
  • Female
  • Gestational Age
  • HLA Antigens / blood*
  • Homozygote
  • Humans
  • Labor Onset / immunology*
  • Pregnancy
  • Pregnancy, Prolonged / immunology*

Substances

  • HLA Antigens