Decreased cord blood IL-4, IL-13, and CCR4 and increased TGF-beta levels after fish oil supplementation of pregnant women

J Allergy Clin Immunol. 2008 Feb;121(2):464-470.e6. doi: 10.1016/j.jaci.2007.09.018. Epub 2007 Nov 5.

Abstract

Background: Altered intakes of n-3 and n-6 polyunsaturated fatty acids were suggested to modulate allergic disease, but intervention trials yielded inconclusive results. Because allergies are primed in early infancy and in utero, the fetus might be more accessible to nutritional intervention strategies.

Objective: We sought to investigate how supplementation of pregnant women with a fish oil (FO) preparation modulates allergy-related immune parameters in mothers and offspring.

Methods: We performed a multicenter, randomized, double-blind, placebo-controlled trial. Three hundred eleven pregnant women received daily either FO with 0.5 g of docosahexaenoic acid and 0.15 g of eicosapentaenoic acid, 400 mug of methyl-tetra-hydrofolic acid, both, or placebo from the 22nd gestational week. T(H)1/T(H)2-related molecules were quantified in 197 maternal and 195 cord blood samples by using real-time RT-PCR. Data are given as geometric means [95% CIs].

Results: FO supplementation was associated with increased TGF-beta mRNA in maternal (0.85 [0.8-0.89]; placebo: 0.68 [0.64-0.72]) and cord blood (0.85 [0.81-0.9]; placebo: 0.75 [0.71-0.79]). IL-1 (0.69 [0.66-0.73]; placebo: 0.83 [0.79-0.88]) and IFN-gamma (0.54 [0.51-0.57]; placebo: 0.65 [0.61-0.69]) were decreased in mothers only (P < .001). Cord blood mRNA levels of IL-4 (0.54 [0.52-0.57]; placebo: 0.64 [0.61-0.68]), IL-13 (0.61 [0.58-0.65]; placebo: 0.85 [0.80-0.89]), CCR4 (0.70 [0.67-0.73]; placebo: 0.88 [0.84-0.92]; all P < .001), and natural killer (P < .001) and CCR3+CD8+ T cells (P < .04) were decreased in the FO group.

Conclusion: Supplementation with FO during pregnancy is associated with decreased mRNA levels of T(H)2-related molecules in the fetus and decreased maternal inflammatory cytokines. We speculate that both effects are mediated by TGF-beta.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cytokines / blood
  • Delivery, Obstetric
  • Dietary Supplements*
  • Docosahexaenoic Acids / pharmacology
  • Double-Blind Method
  • Female
  • Fetal Blood*
  • Fish Oils / pharmacology*
  • Humans
  • Infant, Newborn
  • Inflammation Mediators / blood
  • Interleukin-13 / blood*
  • Interleukin-13 / genetics
  • Interleukin-4 / blood*
  • Interleukin-4 / genetics
  • Lymphocyte Subsets / drug effects
  • Male
  • Pregnancy* / blood
  • RNA, Messenger / blood
  • Receptors, CCR4 / blood*
  • Receptors, CCR4 / genetics
  • Transforming Growth Factor beta / blood*
  • Transforming Growth Factor beta / genetics

Substances

  • CCR4 protein, human
  • Cytokines
  • Fish Oils
  • Inflammation Mediators
  • Interleukin-13
  • RNA, Messenger
  • Receptors, CCR4
  • Transforming Growth Factor beta
  • Interleukin-4
  • Docosahexaenoic Acids