Association between the -159C/T CD14 gene polymorphism and tuberculosis in a Korean population

FEMS Immunol Med Microbiol. 2009 Dec;57(3):229-35. doi: 10.1111/j.1574-695X.2009.00602.x. Epub 2009 Aug 21.

Abstract

The aim of the present study was to confirm the association between the CD14-159C/T polymorphism and tuberculosis in the Korean population and to elucidate the functional basis for this putative association. CD14-159C/T genotypes were determined by PCR - restriction fragment length polymorphism analysis in 274 tuberculosis patients and 422 healthy controls. Recombinant CD14 promoter-luciferase reporter constructs, including the -159T or -159C allele, were transfected into K562 and BEAS-2B cells, and luciferase activities were measured and compared. Levels of serum sCD14 and interferon-gamma secreted by peripheral blood mononuclear cells (PBMCs) were measured using enzyme-linked immunosorbent assay.The frequency of -159TT genotypes was higher in tuberculosis patients than in healthy controls. The promoter activity of the -159T allele was higher than that of the -159C allele. Serum sCD14 levels were higher among tuberculosis patients with -159TT genotypes than among those with -159CC genotypes and interferon-gamma release by PBMCs was decreased in subjects with -159TT genotypes. In conclusion, the -159TT CD14 genotypes were associated with tuberculosis development in Koreans. This association might be a result of the higher promoter activity of the -159T allele, the higher level of sCD14, and the decreased interferon-gamma secretion in subjects with -159TT genotypes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Artificial Gene Fusion
  • Cells, Cultured
  • Female
  • Gene Frequency
  • Genes, Reporter
  • Genetic Predisposition to Disease*
  • Humans
  • Interferon-gamma / metabolism
  • Leukocytes, Mononuclear / immunology
  • Lipopolysaccharide Receptors / blood
  • Lipopolysaccharide Receptors / genetics*
  • Luciferases / genetics
  • Luciferases / metabolism
  • Male
  • Middle Aged
  • Point Mutation*
  • Polymerase Chain Reaction / methods
  • Polymorphism, Genetic*
  • Polymorphism, Restriction Fragment Length
  • Promoter Regions, Genetic*
  • Republic of Korea
  • Tuberculosis / genetics*
  • Tuberculosis / immunology*
  • Young Adult

Substances

  • Lipopolysaccharide Receptors
  • Interferon-gamma
  • Luciferases