Intraepithelial lymphocyte immunophenotype: a useful tool in the diagnosis of celiac disease

J Physiol Biochem. 2018 Feb;74(1):153-158. doi: 10.1007/s13105-017-0586-9. Epub 2017 Aug 16.

Abstract

According to new ESPGHAN guidelines, gluten challenge is considered necessary when there is doubt about the initial diagnosis of celiac disease (CD). The main aim of this study was to quantify intraepithelial lymphocyte (IEL) immunophenotype on celiac patients on gluten-containing diet (GCD) compared to those on gluten-free diet (GFD). Another aim was to evaluate the clinical utility of IELs in the CD diagnosis, especially in selected patients on GFD where diagnostic uncertainty remains. IEL immunophenotype (TCRγδ and NK-like IELs) were studied by flow cytometry in 111 children with CD (81 children with CD on GCD and 30 celiac patients on GFD) and a control group (10 children). Duration of GFD was 5.4 ± 1.6 years. TCRγδ IELs in celiac patients receiving a GCD or GFD were significantly higher (p < 0.001) than in the control group. NK-like IELs in patients receiving a GCD or GFD were significantly lower than in the control group (p < 0.001). We observed a permanent decrease of NK-like IELs and an increment of TCRγδ IELs after following an adequate establishment and compliance of a long-term GFD in celiac patients. Recognition of IELs changes in the intestinal mucosa on celiac patients after long-term establishment of a GFD could constitute a useful tool for CD diagnosis in various situations: in which there is doubt about the initial diagnosis and repeat biopsy is necessary (avoiding the need of gluten challenges), and in those patients with symptoms/signs suggestive of CD who maintain a low gluten diet.

Keywords: Flow cytometry; Mucosal immunology; Pediatric gastroenterology.

MeSH terms

  • Adolescent
  • Asymptomatic Diseases
  • Biopsy
  • Celiac Disease / diagnosis*
  • Celiac Disease / diet therapy
  • Celiac Disease / epidemiology
  • Celiac Disease / pathology
  • Child
  • Child, Preschool
  • Diet, Gluten-Free
  • Female
  • Follow-Up Studies
  • Hospitals, University
  • Humans
  • Immunity, Mucosal
  • Immunophenotyping*
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / pathology
  • Intestine, Small / immunology*
  • Intestine, Small / pathology
  • Intraepithelial Lymphocytes / immunology*
  • Intraepithelial Lymphocytes / pathology
  • Male
  • Retrospective Studies
  • Risk
  • Spain / epidemiology