Tumor necrosis factor alpha gene variants do not display allelic imbalance in circulating myeloid cells

Cell Immunol. 2010;262(2):127-33. doi: 10.1016/j.cellimm.2010.02.004. Epub 2010 Feb 10.

Abstract

Carriage of the TNF -308 A allele (rs1800629 A) has been associated with increased serum TNF-alpha levels, the development of sepsis syndrome, and fatal outcome, in severely traumatized patients (Menges et al., 2008 [1]). Herein, we analysed the putative allelic imbalance of TNF-alpha release from myeloid cells. Circulating peripheral blood cells from healthy human blood donors (n=104) and monocyte-derived macrophages (n=158) were analysed for their ex vivo capacity of TNF-alpha expression. Our findings indicate that carriage of the TNF -308 A allele is not associated with high TNF-alpha expression in circulating human leucocytes and monocyte-derived macrophages. Other cellular sources, e.g. tissue-resident cells like mast cells and/or tissue specific macrophages might be the cellular source of high TNF-alpha serum levels shortly after trauma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Allelic Imbalance*
  • Female
  • Genotype
  • Humans
  • Lipopolysaccharide Receptors / immunology
  • Male
  • Middle Aged
  • Monocytes / cytology
  • Monocytes / immunology
  • Myeloid Cells / cytology
  • Myeloid Cells / physiology*
  • Neutrophils / cytology
  • Neutrophils / immunology
  • Polymorphism, Genetic
  • Promoter Regions, Genetic / genetics
  • Prospective Studies
  • Receptors, IgG / immunology
  • Tumor Necrosis Factor-alpha / genetics*
  • Tumor Necrosis Factor-alpha / metabolism*
  • Young Adult

Substances

  • Lipopolysaccharide Receptors
  • Receptors, IgG
  • Tumor Necrosis Factor-alpha