Hyper-responsive T-cell cytokine profile in association with development of early childhood wheeze but not eczema at 2 years

Asian Pac J Allergy Immunol. 2014 Mar;32(1):84-92. doi: 10.12932/AP0355.32.1.2014.

Abstract

Background: Eczema is a known risk factor for the development of wheeze in childhood. Cord blood T-cell cytokine responses have been shown to be associated with the development of both early childhood eczema and wheeze. Our objective is to study and compare the influence of intrinsic T-cell cytokine responses on the development of wheezing and eczema in the first 2 years of life in a birth cohort of at risk (first degree family with atopic disease) infants.

Methods: Cord blood samples were collected from 195 eligible subjects of a birth cohort of 253 subjects. The subjects studied were those who developed either wheezing (n = 34) or eczema (n = 29) in the first 2 years of life, and 65 healthy infants served as control. Cytokines from phytohaemagglutinin stimulated mononuclear cells were analyzed using multiplex cytokine assays and the cytokine profiles in the 3 groups were compared.

Results: Most of the subjects were non-atopic with only 3/34 (9%) wheeze and 9/29 (31%) eczema subjects sensitized to the common dietary or inhalant allergens. After adjustment for potential risk factors, wheeze, but not eczema subjects, presented with hyper-responsive cytokine profiles with increased production of T-cell cytokines IL-2 and IL-5. IL-5 was the strongest risk factor associated to the development of wheeze at 2 years of age (OR, 35; 95% CI, 5.0 -246.7).

Conclusion: Cord blood cytokine responses in early onset wheeze and eczema are distinctly different. This suggests that the tendency to develop early onset wheeze may be influenced by preexisting immune factors independent to those for eczema.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child, Preschool
  • Eczema / etiology
  • Eczema / immunology*
  • Fetal Blood / immunology
  • Humans
  • Hypersensitivity, Immediate / immunology*
  • Infant
  • Interleukin-2 / immunology*
  • Interleukin-5 / immunology*
  • Respiratory Sounds / etiology*
  • Respiratory Sounds / immunology*
  • Risk Factors
  • T-Lymphocytes / immunology*

Substances

  • Interleukin-2
  • Interleukin-5