Lower Cord Blood IL-17 and IL-25, but Not Other Epithelial Cell-Derived Cytokines Are Associated with Atopic Dermatitis in Infancy

Int Arch Allergy Immunol. 2021;182(6):474-478. doi: 10.1159/000512919. Epub 2021 Jan 7.

Abstract

Background: There is a growing need for early biomarkers that may predict the development of atopic dermatitis (AD). As alterations in skin barrier may be a primary event in disease pathogenesis, epithelial cell (EC) cytokines expression patterns may be a potential biomarker in early life to target allergy preventive strategies towards "at-risk" infants.

Objectives: The aim of this longitudinal investigation was to examine from birth over the course of infancy levels of the EC cytokines: thymic stromal lymphopoietin (TSLP), interleukin (IL)-33, IL-25, and IL-17 in infants at high-risk of AD due to maternal atopy.

Method: We collected (n = 31) cord blood samples from atopic mothers and followed up their infants at 4-6 and 12 months of age for collection of peripheral venous blood samples and diagnosis of AD. TSLP concentration was measured by ELISA after acetone precipitation of the samples. IL-33, IL-25, and IL-17 levels were measured by Luminex.

Results: Seven infants who developed AD had lower levels of IL-25 and IL-17 at birth compared to the 24 infants who did not develop AD by 12 months of age.

Conclusions: Lower cord blood levels of IL-17 and IL-25, but not other EC cytokines, were associated with the onset of AD during infancy. Our results highlight that the in-utero period appears critical, and potential maternal influences on cord blood EC-derived cytokine concentrations requires further exploration.

Keywords: Allergy prevention; Atopic dermatitis; Cord blood; Epithelial cell cytokines; Infancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers
  • Cytokines / blood*
  • Dermatitis, Atopic / blood*
  • Dermatitis, Atopic / diagnosis*
  • Dermatitis, Atopic / etiology
  • Epithelial Cells / metabolism*
  • Female
  • Fetal Blood*
  • Humans
  • Infant
  • Interleukin-17 / blood*
  • Maternal Exposure / adverse effects
  • Pregnancy
  • Prenatal Exposure Delayed Effects
  • Prognosis
  • Thymic Stromal Lymphopoietin

Substances

  • Biomarkers
  • Cytokines
  • IL17A protein, human
  • IL25 protein, human
  • Interleukin-17
  • Thymic Stromal Lymphopoietin