Plasma levels of immunosuppressive mediators during cardiopulmonary bypass

E Borrelli1, P Giomarelli, A Naldini

  • 1Institute of Thoracic and Cardiovascular Surgery Via Laterina University of Siena Siena 8 - 53100 Siena Italy.

Insights

Cardiopulmonary bypass (CPB) significantly increases immunosuppressive mediators like complement fraction C3a and transforming growth factor-beta(1). These changes correlate with a suppressed immune cell proliferation during CPB procedures.

Area of Science:

  • Immunology
  • Cardiovascular Surgery

Background:

  • Extracorporeal circulation, particularly cardiopulmonary bypass (CPB), is associated with significant immunological alterations.
  • Understanding the mediators involved in CPB-induced immunosuppression is crucial for patient outcomes.

Purpose of the Study:

  • To evaluate plasma levels of complement fraction C3a (C3a) and transforming growth factor-beta(1) (TGF-beta(1)) during extracorporeal circulation.
  • To assess the impact of CPB on the proliferation of peripheral blood mononuclear cells (PBMCs).

Main Methods:

  • Study included 16 patients undergoing hypothermic or normothermic CPB and 4 controls without CPB.
  • Blood samples were collected at multiple time points: pre-CPB, during CPB (every 30 min), post-CPB, and post-protamine administration.
  • Plasma levels of C3a and TGF-beta(1) were measured, and PBMC proliferation after phytohaemagglutinin (PHA) stimulation was assessed.

Main Results:

  • Both C3a and TGF-beta(1) levels significantly increased during and after CPB in both hypothermic and normothermic groups.
  • The increase in C3a and TGF-beta(1) was more prominent in the normothermic group, but not statistically significant compared to the hypothermic group.
  • PBMC proliferation index decreased significantly within 30 minutes of CPB initiation and remained suppressed throughout the procedure.

Conclusions:

  • Elevated plasma levels of C3a and TGF-beta(1) suggest their involvement in the immunosuppressive effects observed during extracorporeal circulation.
  • These findings highlight a potential role for C3a and TGF-beta(1) in mediating immunological changes associated with CPB.