Expression pattern of T-helper 17 cell signaling pathway and mucosal inflammation in celiac disease

Scand J Gastroenterol. 2014 Feb;49(2):145-56. doi: 10.3109/00365521.2013.863966. Epub 2013 Dec 10.

Abstract

Objective: The aim was to investigate the mucosal activation of a broad range of genes associated with the T-helper 17 cell (Th17) signaling pathway in children at different stages of celiac disease (CD), including children with increased risk for CD and children with untreated and gluten-free diet (GFD)-treated CD.

Material and methods: Small intestinal biopsies were taken from children with untreated and GFD-treated CD, transglutaminase antibody (TGA)-positive children with potential CD, and reference children. Real-time polymerase chain reaction (PCR) arrays were used to study the gene expression pattern of Th17-related genes, and quantitative PCR was used to study the interleukin (IL)-17A expression.

Results: The mucosal expression of CD8A was elevated at all stages of CD. Children with untreated CD had diminished levels of IL-17RE, IL-23R, RORc, STAT6, CCL22, NFATC2, IL-18, CD4, CD247, and matrix metalloproteinase (MMP)9 but had elevated levels of MMP3, IL-17, interferon-γ (IFN-γ) and CD8A, compared to references. The majority of the aforementioned genes, being differentially expressed in untreated CD, displayed similar expression in GFD-treated children and references. Children with untreated and GFD-treated CD had elevated expression of IFN-γ but had reduced expression of CD247. Interestingly, children with potential CD displayed reduced FOXP3, IL-21, and IL-17A levels.

Conclusion: Mucosal upregulation of Th17 immunity occurs at the late stage of disease and is downregulated with dietary treatment, thus indicating that IL-17 immunity is not a fundamental feature of CD as Th1 immunity, which is not fully downregulated by GFD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Antibodies / blood
  • Antigens, CD / genetics*
  • Case-Control Studies
  • Celiac Disease / diet therapy
  • Celiac Disease / genetics*
  • Celiac Disease / immunology
  • Child
  • Child, Preschool
  • Enteritis / genetics
  • Enteritis / immunology
  • Female
  • GTP-Binding Proteins
  • Gene Expression*
  • Humans
  • Infant
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / pathology
  • Male
  • Matrix Metalloproteinase 3 / genetics
  • Matrix Metalloproteinase 9 / genetics
  • Protein Glutamine gamma Glutamyltransferase 2
  • Receptors, Interleukin / genetics*
  • Signal Transduction / genetics*
  • Th17 Cells / metabolism*
  • Transcription Factors / genetics*
  • Transglutaminases / immunology

Substances

  • Antibodies
  • Antigens, CD
  • Intercellular Signaling Peptides and Proteins
  • Receptors, Interleukin
  • Transcription Factors
  • Protein Glutamine gamma Glutamyltransferase 2
  • Transglutaminases
  • Matrix Metalloproteinase 3
  • Matrix Metalloproteinase 9
  • GTP-Binding Proteins