Deficiency of invariant natural killer T cells in coeliac disease

Gut. 2007 Jun;56(6):790-5. doi: 10.1136/gut.2006.095307. Epub 2006 Nov 24.

Abstract

Background: Immunoregulatory invariant natural killer (iNK) T cells rapidly produce interleukin (IL)-4 and other cytokines that suppress a Th1 response and are deficient in some autoimmune diseases.

Aim: The aim of this study was to investigate any deficiency of iNK T cells in coeliac disease.

Methods: Blood was collected from 86 subjects with coeliac disease and from 152 healthy control subjects for investigation of Valpha24+ T cells by flow cytometry. iNK T cells were assessed by Valpha24 and alpha-galactosylceramide/CD1d tetramer markers in 23 normal controls and 13 subjects with coeliac disease. Intracellular IL-4 was measured after anti-CD3 antibody stimulation. Duodenal biopsies were obtained in a subgroup of subjects with coeliac disease and control subjects for Valpha24 mRNA expression using relative PCR and for Valpha24+ T cells by immunofluorescence.

Results: The mean numbers of circulating Valpha24+ T cells and iNK T cells in coeliac disease were 27% (p<0.001) and 16% (p<0.001), respectively, of levels in control subjects. After in vitro anti-CD3 stimulation, numbers of IL-4+ producing iNK T cells from subjects with coeliac disease were unchanged but increased by 21% in control subjects. In subjects with coeliac disease, Valpha24 mRNA intestinal expression was reduced to 17% (p<0.001) by relative PCR and numbers of intestinal Valpha24+ T cells were 16% (p<0.01) of levels in control subjects.

Conclusions: We conclude that Valpha24+ T cells and iNK T cells are deficient in coeliac disease. We speculate that this deficiency could contribute to the failure of immunological oral tolerance that seems to underlie this disease.

MeSH terms

  • Adult
  • Aged
  • Antigens, Differentiation, B-Lymphocyte / analysis*
  • Antigens, Differentiation, B-Lymphocyte / genetics
  • Celiac Disease / immunology*
  • Cells, Cultured
  • Duodenum / immunology
  • Gene Expression
  • Histocompatibility Antigens Class II / analysis*
  • Histocompatibility Antigens Class II / genetics
  • Humans
  • Interleukin-4 / biosynthesis
  • Killer Cells, Natural / immunology*
  • Lymphocyte Count
  • Middle Aged
  • RNA, Messenger / genetics
  • T-Lymphocyte Subsets / immunology*

Substances

  • Antigens, Differentiation, B-Lymphocyte
  • Histocompatibility Antigens Class II
  • RNA, Messenger
  • invariant chain
  • Interleukin-4