Secretion of soluble ST2 - possible explanation for systemic immunosuppression after heart surgery

Thorac Cardiovasc Surg. 2009 Feb;57(1):25-9. doi: 10.1055/s-2008-1039044. Epub 2009 Jan 23.

Abstract

Background: Cardiopulmonary bypass is known to affect cytokine release leading to a generalized endogenous immune reaction similar to that described in sepsis, without having been explored in great detail. Therefore we evaluated the anti- and pro-inflammatory cytokine responses after heart surgery.

Methods: 16 patients who underwent coronary artery bypass graft (CABG) surgery with extracorporeal circulation were included. ST2, IL-4 and IL-10 served as markers for TH2 cytokine response; IL-6, IL-8 and IFN-gamma as TH1 markers. Furthermore, total immunoglobulin subtype analysis (IgM, IgG, IgE) was performed.

Results: Serum levels of soluble ST2 started to climb at 60 minutes (from 38 +/- 14 preoperatively to 1 480 +/- 890 pg/ml) and peaked 24 hours after surgery (13 360 +/- 2 840 pg/ml, P < 0.001). IL-10 reached a maximum at 60 minutes and returned to baseline levels 24 hours later. IL-6 and IL-8 levels peaked 60 minutes after surgery. IL-4 and IFN-gamma did not change. Only IgM showed a significant peak on day eight ( P < 0.001).

Conclusion: Our results demonstrate that CABG surgery induces a massive long-lasting secretion of ST2, a protein related to immune suppression.

MeSH terms

  • Cardiopulmonary Bypass / adverse effects*
  • Coronary Artery Bypass / adverse effects*
  • Coronary Artery Disease / surgery*
  • Cytokines / blood
  • Female
  • Humans
  • Immune Tolerance*
  • Immunoglobulins / blood
  • Interleukin-1 Receptor-Like 1 Protein
  • Male
  • Middle Aged
  • Receptors, Cell Surface / blood*
  • Th1 Cells / immunology
  • Th2 Cells / immunology
  • Time Factors
  • Up-Regulation

Substances

  • Cytokines
  • IL1RL1 protein, human
  • Immunoglobulins
  • Interleukin-1 Receptor-Like 1 Protein
  • Receptors, Cell Surface