Risk of allergy development correlates with IL-4 receptor expression on newborns' monocytes and Th lymphocytes

Med Sci Monit. 2007 Oct;13(10):CR445-8.

Abstract

Background: IL-4 receptor (IL-4R) overexpression on immunoregulatory/effector cells was found in allergic patients. However, its role in allergy development remains unclear. The aim of this study was to assess the correlation between IL-4R expression and allergy development within the first year of life.

Material/methods: IL-4R expression on monocytes and Th lymphocytes of 43 newborns was analyzed using flow cytometry. Plasma levels of IL-4, -12 and IFN-gamma were also measured using ELISA. The same parameters were assessed one year later. Furthermore, clinical evaluation was performed every three months for one year.

Results: Mean IL-4R expression on monocytes and Th lymphocytes did not differ at birth. After one year it increased on Th-lymphocytes and decreased on monocytes. However, among 10 children with severe atopy during the observation period, 8 displayed IL-4R above the mean value for the group on both monocytes and Th cells at birth as well as one year later. No correlation was found between IL-4 or IFN-gamma and IL-4R expression at birth. After one year, significant IL-4 increases and IFN-gamma decreases were observed which correlated with IL-4R expression. IL-4R expression on the newborns' monocytes correlated negatively with IL-12 plasma level; however, it was statistically significant only in the children developing allergy. Moreover, only in these patients was a significant decrease in IL-12 found after one year.

Conclusions: IL-4R-dependent over-signaling in newborns' monocytes and Th lymphocytes could contribute to Th1/Th2 imbalance. IL-4R overexpression on newborns' monocytes and lymphocytes could be an early risk marker of allergy development.

MeSH terms

  • Cell Separation
  • Cytokines / blood
  • Humans
  • Hypersensitivity / immunology*
  • Infant
  • Infant, Newborn
  • Lipopolysaccharide Receptors / metabolism
  • Monocytes / cytology
  • Monocytes / immunology*
  • Receptors, Interleukin-4 / immunology*
  • Risk Factors
  • T-Lymphocytes, Helper-Inducer / cytology
  • T-Lymphocytes, Helper-Inducer / immunology*

Substances

  • Cytokines
  • Lipopolysaccharide Receptors
  • Receptors, Interleukin-4