Study on serum TL1A levels and their correlation with Th17 cells, IL-17 and IL-21 in children with Graves' disease

Front Immunol. 2024 Dec 13:15:1455025. doi: 10.3389/fimmu.2024.1455025. eCollection 2024.

Abstract

Objective: To investigate serum TL1A levels and their correlation with Th17 cells, IL-17, and IL-21 in children with Graves' disease (GD).

Methods: Thirty-seven children (12 males and 25 females) aged 9-14 years with newly diagnosed and untreated GD were enrolled in this study. Serum TL1A, IL-17, and IL-21 levels were measured using enzyme-linked immunosorbent assay (ELISA). The percentage of Th17 cells in peripheral blood was determined by flow cytometry. The correlation between serum TL1A levels and Th17 cells, IL-17, and IL-21 was analyzed using Pearson's correlation coefficient.

Results: Serum TL1A levels and the percentage of Th17 cells were significantly higher in children with GD compared to healthy controls (P<0.05). Serum IL-17 and IL-21 levels were also significantly elevated in GD patients (P<0.05). Serum TL1A levels positively correlated with the percentage of Th17 cells (r=0.625, P<0.05), IL-17 (r=0.573, P<0.05), and IL-21 (r=0.542, P<0.05) in children with GD.

Conclusion: Serum TL1A levels are increased in children with GD and positively correlate with Th17 cells, IL-17, and IL-21, suggesting that TL1A may play a role in the pathogenesis of GD by regulating Th17 cell differentiation and the production of IL-17 and IL-21.

Keywords: Graves’ disease; IL-17; IL-21; TL1A; Th17 cells; children.

MeSH terms

  • Adolescent
  • Biomarkers / blood
  • Child
  • Female
  • Graves Disease* / blood
  • Graves Disease* / immunology
  • Humans
  • Interleukin-17* / blood
  • Interleukins* / blood
  • Male
  • Th17 Cells* / immunology
  • Th17 Cells* / metabolism
  • Tumor Necrosis Factor Ligand Superfamily Member 15* / blood

Substances

  • interleukin-21
  • Interleukins
  • Interleukin-17
  • Tumor Necrosis Factor Ligand Superfamily Member 15
  • TNFSF15 protein, human
  • IL17A protein, human
  • Biomarkers

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported by the National Natural Science Foundation of China (No. 81903340).