PMID- 14506092 OWN - NLM STAT- MEDLINE DCOM- 20040914 LR - 20131121 IS - 8750-7587 (Print) IS - 0161-7567 (Linking) VI - 96 IP - 2 DP - 2004 Feb TI - Interferon-gamma increases monocyte HLA-DR expression without effects on glucose and fat metabolism in postoperative patients. PG - 597-603 AB - Tissue injury is associated with decreased cellular immunity and enhanced metabolism. Immunodepression is thought to be counteracted by interferon (IFN)-gamma, which increases human leukocyte antigen (HLA)-DR expression. Hypermetabolism could be enhanced by IFN-gamma because cytokines induce a hypermetabolic response to stress. In healthy humans, IFN-gamma enhanced HLA-DR expression without effects on glucose and fat metabolism. In the present study, we evaluated whether IFN-gamma lacks potential harmful side effects on metabolic and endocrine pathways while maintaining its beneficial effects on the immune system under conditions in which the inflammatory response system is activated. In 13 patients scheduled for major surgery, we studied HLA-DR expression on peripheral blood monocytes before surgery and postoperatively randomized the patients into an intervention and a placebo group. Subsequently, we evaluated the effects of a single dose of IFN-gamma vs. saline on short-term monocyte activation, glucose and lipid metabolism, and glucose and lipid regulatory hormones. HLA-DR expression on monocytes was restored from postoperative levels of 54% (42-60%; median and interquartiles) to 92% (91-96%) 24 h after IFN-gamma administration but stayed low in the placebo-treated patients. IFN-gamma did not affect glucose metabolism (plasma glucose, rate of appearance and disappearance of glucose) and lipid metabolism (plasma glycerol, plasma free fatty acids, and rates of appearance and disappearance of glycerol). IFN-gamma had no effect on plasma cortisol, adrenocorticotropic hormone, growth hormone, insulin, C-peptide, glucagon, epinephrine, and norepinephrine concentrations. We conclude that IFN-gamma exerts a favorable effect on cell-mediated immunity in patients after major surgery without effects on glucose and lipid metabolism. FAU - de Metz, Jesse AU - de Metz J AD - Department of Endocrinology and Metabolism, Academic Medical Center, 1100 DD Amsterdam, The Netherlands. FAU - Romijn, Johannes A AU - Romijn JA FAU - Endert, Erik AU - Endert E FAU - Ackermans, Mariette T AU - Ackermans MT FAU - Weverling, Gerrit Jan AU - Weverling GJ FAU - Busch, Olivier R AU - Busch OR FAU - de Wit, Laurence Th AU - de Wit LT FAU - Gouma, Dirk J AU - Gouma DJ FAU - ten Berge, Ineke J M AU - ten Berge IJ FAU - Sauerwein, Hans P AU - Sauerwein HP LA - eng PT - Clinical Trial PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't DEP - 20030923 PL - United States TA - J Appl Physiol (1985) JT - Journal of applied physiology (Bethesda, Md. : 1985) JID - 8502536 RN - 0 (Antineoplastic Agents) RN - 0 (Blood Glucose) RN - 0 (HLA-DR Antigens) RN - 0 (Hormones) RN - 82115-62-6 (Interferon-gamma) RN - PDC6A3C0OX (Glycerol) SB - IM MH - Aged MH - Antineoplastic Agents/*administration & dosage MH - Blood Glucose/drug effects/*metabolism MH - Energy Metabolism/drug effects MH - Female MH - Glycerol/metabolism MH - HLA-DR Antigens/*metabolism MH - Hormones/blood MH - Humans MH - Interferon-gamma/*administration & dosage MH - *Lipid Metabolism MH - Male MH - Middle Aged MH - Monocytes/*drug effects/metabolism MH - Postoperative Period EDAT- 2003/09/25 05:00 MHDA- 2004/09/15 05:00 CRDT- 2003/09/25 05:00 PHST- 2003/09/25 05:00 [pubmed] PHST- 2004/09/15 05:00 [medline] PHST- 2003/09/25 05:00 [entrez] AID - 00090.2002 [pii] AID - 10.1152/japplphysiol.00090.2002 [doi] PST - ppublish SO - J Appl Physiol (1985). 2004 Feb;96(2):597-603. doi: 10.1152/japplphysiol.00090.2002. Epub 2003 Sep 23.