Graft protein C entrapment is associated with reduced phagocyte activation during reperfusion in human liver transplantation

Crit Care Med. 2006 Feb;34(2):426-32. doi: 10.1097/01.ccm.0000198108.38349.28.

Abstract

Objective: To explore the potential anti-inflammatory role of protein C pathway in ischemia-reperfusion injury during liver transplantation.

Design: Prospective, observational clinical study.

Setting: Tertiary teaching hospital.

Patients: Fifty adult patients undergoing liver transplantation for acute liver failure or chronic liver disease.

Interventions: To assess changes occurring across the transplanted liver, samples of blood entering and leaving the graft were obtained simultaneously from portal and hepatic veins. Plasma protein C and activated protein C levels, neutrophil and monocyte CD11b and L-selectin expression, and leukocyte differential counts were measured. Postoperative liver function and outcome of transplantation were recorded.

Measurements and main results: During reperfusion, protein C became entrapped within the graft (portal vein 49% [20-96%]; graft caval effluent 25% [12-76%], p < .001), without concomitant activated protein C outflow from the graft. Simultaneously, marked neutrophil and monocyte activation occurred within the graft. Enhanced hepatic protein C entrapment was associated with reduced neutrophil and monocyte activation (R = .377, p = .011; R = .389, p = .008, respectively) during reperfusion.

Conclusions: Protein C entrapment occurs immediately during reperfusion in the graft without concomitant activated protein C release, suggesting a shortage of activated protein C in the reperfused graft. The ongoing inflammatory response during reperfusion may lead to protein C and activated protein C utilization within the graft. Indeed, hepatic protein C entrapment is associated with reduced hepatic phagocyte activation, suggesting a regulatory role for protein C pathway in hepatic reperfusion in human liver transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Humans
  • Liver Transplantation*
  • Male
  • Middle Aged
  • Neutrophils / metabolism
  • Phagocytes / metabolism*
  • Phagocytes / physiology
  • Protein C / metabolism
  • Protein C / physiology*
  • Reperfusion Injury / blood*
  • Reperfusion Injury / metabolism

Substances

  • Protein C