Quantitative flow cytometry to measure the TNF-alpha and IL-2 system after heart transplantation

Transpl Int. 2000:13 Suppl 1:S212-5. doi: 10.1007/s001470050327.

Abstract

After heart transplantation a high incidence of infections and malignancies is found. Not only immunosuppression, but also intrinsic cytokine systems with some unbalance, e. g. TNF-alpha and IL-2, can result in impaired immune competence and may have a role in these complications. The aim of this study was to assess the activity of the TNF-alpha and IL-2 systems after heart transplantation. In peripheral blood we measured expression of activation markers of TNF-alpha (TNF-R2) and IL-2 (IL-2R alpha, IL-2R beta-chain) on monocytes and lymphocytes using quantitative flow-cytometric analysis. TNF-R2 expression was significantly enhanced on monocytes and lymphocytes in patients after heart transplantation, while the expression of IL-2R alpha and IL-2R beta was not elevated. Increased TNF-R2 expression in peripheral blood after heart transplantation reflects an activated TNF-alpha system, leading to high levels of active sTNF-R, which impairs TNF-alpha bioavailibility and consequently leads to immune incompetence.

MeSH terms

  • Adult
  • Aged
  • Antigens, CD / blood
  • Female
  • Flow Cytometry / methods
  • Heart Transplantation / immunology*
  • Heart Transplantation / physiology
  • Humans
  • Interleukin-2 / blood*
  • Lymphocytes / immunology
  • Male
  • Middle Aged
  • Monocytes / immunology
  • Receptors, Interleukin-2 / blood
  • Receptors, Tumor Necrosis Factor / blood
  • Receptors, Tumor Necrosis Factor, Type II
  • Tumor Necrosis Factor-alpha / analysis*

Substances

  • Antigens, CD
  • Interleukin-2
  • Receptors, Interleukin-2
  • Receptors, Tumor Necrosis Factor
  • Receptors, Tumor Necrosis Factor, Type II
  • Tumor Necrosis Factor-alpha