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Neutrophil respiratory burst following liver transplantation: in vitro effects of granulocyte colony‐stimulating factor
Author(s) -
Jaeger K.,
Ruschulte H.,
Heine J.,
Scheinichen D.,
Leuwer M.,
Winkler M.,
Kuse E.R.
Publication year - 1999
Publication title -
transplant infectious disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.69
H-Index - 67
eISSN - 1399-3062
pISSN - 1398-2273
DOI - 10.1034/j.1399-3062.1999.010303.x
Subject(s) - medicine , respiratory burst , sepsis , granulocyte , granulocyte colony stimulating factor , immunology , stimulation , liver transplantation , flow cytometry , priming (agriculture) , cytokine , in vitro , transplantation , tumor necrosis factor alpha , neutrophil extracellular traps , pharmacology , gastroenterology , inflammation , chemotherapy , biology , biochemistry , botany , germination
Early postoperative infections and septic complications are predominant causes of morbidity and mortality in patients following orthotopic liver transplantation (OLTx). Prophylactic granulocyte colony‐stimulating factor (G‐CSF) administration after OLTx was found to decrease the number of sepsis episodes and sepsis‐related mortality. Since polymorphonuclear neutrophils (PMNs) are one of the major determinants of antimicrobial defense, alteration of their functions may influence the development of sepsis in these patients. Therefore, we investigated in vitro whether or not priming with G‐CSF affects the neutrophils’ respiratory burst (RB) in immunosuppressed liver‐transplanted patients. Venous blood was drawn from liver allograft recipients ( n =12) between the 5th and 15th day postoperatively. Patients without clinical signs of infection or rejection were included in this study. Leukocytes were obtained as supernatant following sedimentation and incubated with 1000 IE ml −1 G‐CSF. The RB was measured by the intracellular oxidation of non‐fluorescent dihydrorhodamine to the fluorescent rhodamine by flow cytometry. The results were expressed as a percentage of increasing stimulation compared to the control responses, which are made up of the percentage of cells with RB reaction after stimulation with phorbol ester (PMA), bacteria ( E. coli ), or the combination of a cytokine (TNF‐α) and a bacterial peptide (FMLP) in the absence of G‐CSF. In vitro priming with G‐CSF resulted in significantly increased activity of the RB after PMA (from 71.7% to 85.6%) and TNF‐α/FMLP (from 58.4% to 72.7%) stimulation. These data demonstrate that G‐CSF in vitro augments the RB of PMNs, thereby suggesting a possible therapeutic role for G‐CSF as immunomodulating agent during bacterial and fungal infections following OLTx.