Maternal trans-vaccenic acid shapes neonatal T cell development and early-life immune imprinting

Science. 2026 Jun 18;392(6804):eaea4041. doi: 10.1126/science.aea4041. Epub 2026 Jun 18.

Abstract

How maternal nutrition influences neonatal immune development and imprinting through breastfeeding remains largely unclear. We report that maternal supplementation with trans-vaccenic acid (TVA), the predominant naturally occurring trans-fatty acid in human breast milk, promoted neonatal T cell development in mice. Neonates fed by mothers on a TVA-enriched diet showed an expanded naïve cluster of differentiation 4 (CD4+) T cell population and enhanced adaptive immunity against infection. TVA reprogrammed neonatal naïve CD4+ T cells through a G protein-coupled receptor-CCCTC-binding factor axis and promoted T helper cells (Th1)-skewing by cooperating with the transcription factor TBX21. Early-life exposure to maternal TVA via breastfeeding supported long-lasting antiviral immunity in adulthood. Our findings establish the multifaceted benefits of maternal nutrition and breastfeeding via TVA in promoting infant immune homeostasis and protective immunity.

MeSH terms

  • Adaptive Immunity*
  • Animals
  • Animals, Newborn / immunology
  • Breast Feeding
  • CD4-Positive T-Lymphocytes* / immunology
  • Dietary Supplements
  • Female
  • Humans
  • Maternal Nutritional Physiological Phenomena*
  • Mice
  • Mice, Inbred C57BL
  • Oleic Acids* / administration & dosage
  • Oleic Acids* / pharmacology
  • Receptors, G-Protein-Coupled / metabolism
  • T-Box Domain Proteins / metabolism
  • T-bet Transcription Factor
  • Th1 Cells* / immunology

Substances

  • 11-octadecenoic acid
  • Oleic Acids
  • Receptors, G-Protein-Coupled
  • T-bet Transcription Factor
  • T-Box Domain Proteins