Intrauterine growth restriction and prematurity influence regulatory T cell development in newborns

J Pediatr Surg. 2014 May;49(5):727-32. doi: 10.1016/j.jpedsurg.2014.02.055. Epub 2014 Feb 22.

Abstract

Purpose: The aim of this study was to determine the relationship of birth weight and gestational age with regulatory T cells (Tregs) in cord blood of human newborns.

Methods: Cord blood mononuclear cells (CBMCs) of 210 newborns were analyzed using flow cytometry to identify Tregs (CD3(+), CD4(+), CD25(high), FoxP3(high)) and measure FoxP3 mean fluorescence intensity (MFI). Suppressive index (SI) was calculated as FoxP3 MFI per Treg.

Results: Mode of delivery had no significant effect on Tregs at birth. Term babies with growth restriction had fewer Tregs than their appropriate weight counterparts but equivalent SI. Preterm babies had higher percentages of Tregs, but lower SI than term controls. SI steadily increased through gestation.

Conclusions: Intrauterine growth restriction is correlated with fewer circulating Tregs and prematurity with decreased functionality of Tregs compared to term appropriate weight infants. This may have implications in diseases such as necrotizing enterocolitis that disproportionately affect premature and lower birth weight infants.

Keywords: Cord blood; Intrauterine growth restriction; Newborns; Prematurity; Regulatory T cells.

MeSH terms

  • Birth Weight
  • CD3 Complex / blood
  • CD4 Antigens / blood
  • Fetal Blood / immunology*
  • Fetal Growth Retardation / immunology*
  • Flow Cytometry
  • Forkhead Transcription Factors / blood
  • Gestational Age
  • Humans
  • Infant, Premature / immunology*
  • Interleukin-2 Receptor alpha Subunit / blood
  • Prospective Studies
  • T-Lymphocytes, Regulatory / metabolism*

Substances

  • CD3 Complex
  • CD4 Antigens
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Interleukin-2 Receptor alpha Subunit