Triplet repeat polymorphism in the transmembrane region of the MICA gene in celiac disease

Tissue Antigens. 2002 Mar;59(3):219-22. doi: 10.1034/j.1399-0039.2002.590307.x.

Abstract

Celiac disease (CD) is characterized by a striking expansion of gamma delta T cells in the intestine. These cells interact with MICA, a cell surface protein encoded by a major histocompatibility complex gene. We investigated whether MICA gene polymorphism could contribute to susceptibility to CD. DNA typing for HLA-DR, DQA1, DQB1, TNF-308, TNFa, TNFb and a triplet repeat polymorphism in the transmembrane region of the MICA gene were carried out. We performed case-control stratified association studies and transmission disequilibrium tests. Our results indicate that although there is no primary association between MICA polymorphism and CD, there is, in addition to HLA-DQ, a second susceptibility locus on the 8.1 ancestral haplotype in strong linkage disequilibrium with MICA A5.1 allele.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Case-Control Studies
  • Celiac Disease / complications
  • Celiac Disease / genetics*
  • Celiac Disease / metabolism
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Histocompatibility Antigens Class I / genetics*
  • Histocompatibility Antigens Class I / metabolism
  • Humans
  • Membrane Proteins / genetics*
  • Phenotype
  • Polymorphism, Genetic*
  • Spain
  • Trinucleotide Repeats / genetics*

Substances

  • Histocompatibility Antigens Class I
  • MHC class I-related chain A
  • Membrane Proteins