Administering granulocyte colony-stimulating factor to acute liver failurepatients corrects neutrophil defects

Objectives Neutrophil function is defective in acute liver failure (ALF) an d the in vitro ability of granulocyte colony-stimulating factor (G-CSF) to reverse these defects has been reported. The effects of administering G-CSF to ALF patients are presented in this study. Design This was a prospective, phase I/II, open label, study. Setting The liver intensive therapy unit at King's College Hospital, London . Participants Sequential patients admitted with acute liver failure due to a cetaminophen overdose. Interventions G-CSF was given to four groups (each n = 6) of ALF patients a s a daily infusion at 25, 50, 100 or 150 mug/m(2). A control group of eight patients did not receive G-CSF. Main outcome measures Neutrophil phagocytosis and killing of Staphylococcus aureus and superoxide release before G-CSF administration and at 24 and 96 h thereafter. Results Neutrophils from patients receiving 50, 100 or 150 mug/m(2) G-CSF, but not from control patients or those receiving 25 mug/m(2), showed signif icantly increased phagocytosis and killing at 96 h, Doses of 50 or 150 mug/ m(2) G-CSF resulted in increased superoxide production at 96 h. No patients discontinued treatment as a consequence of side effects related to G-CSF a dministration. Conclusions G-CSF administration is a safe and effective means of reversing the neutrophil defects of ALF, and may have a role in the prevention and t reatment of infection in these patients. A dose of 50 mug/m(2)/day is as ef fective as higher doses and was associated with fewer side effects. Eur J G astroenterol Hepatol 12:1323-1328 (C) 2000 Lippincott Williams & Wilkins.