Interleukin-17A Levels Increase in Serum of Children With Juvenile Idiopathic Arthritis

Gordana Vijatov-Djuric1,2, Aleksandra Doronjski1,2, Igor Mitic1,3

  • 1Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia.

Archives of Rheumatology
|October 31, 2018
PubMed

Insights

Serum interleukin-17A (IL-17A) levels are elevated in children with juvenile idiopathic arthritis (JIA). Higher IL-17A levels correlate with increased disease activity and specific clinical features, aiding early risk detection in JIA patients.

Area of Science:

  • Immunology
  • Pediatric Rheumatology
  • Biomarker Discovery

Background:

  • Juvenile idiopathic arthritis (JIA) is a chronic inflammatory condition in children.
  • Interleukin-17A (IL-17A) is a pro-inflammatory cytokine implicated in autoimmune diseases.
  • Understanding IL-17A's role in JIA may offer insights into disease pathogenesis and progression.

Purpose of the Study:

  • To quantify serum IL-17A levels in children diagnosed with JIA.
  • To investigate the association between IL-17A levels and JIA disease activity.
  • To explore correlations between IL-17A and clinical/laboratory markers of inflammation in JIA.

Main Methods:

  • Serum samples were collected from 30 children with active JIA and 30 age/sex-matched healthy controls.
  • Enzyme-linked immunosorbent assay (ELISA) was employed to measure serum IL-17A concentrations.
  • Clinical assessments included disease activity scores, joint involvement, and inflammatory markers (ESR, CRP).

Main Results:

  • Children with JIA exhibited significantly higher serum IL-17A levels compared to healthy controls.
  • IL-17A levels decreased significantly in JIA patients who achieved inactive disease.
  • Elevated IL-17A correlated with increased coxofemoral joint arthritis, higher ESR and CRP levels, and greater JADAS-27 scores.

Conclusions:

  • Serum IL-17A is a potential biomarker for active inflammation in JIA.
  • Measuring IL-17A in early JIA may help identify children at risk of poor functional outcomes.
  • Targeting IL-17A pathways could be a future therapeutic strategy for JIA management.
Abstract

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