Effects of r-metHuG-CSF on polymorphonuclear leucocyte kinetics and function in patients on continuous ambulatory

J Turzanski1, S P Crouch, M Andrews

  • 1The David Evans Medical Research Centre, City Hospital NHS Trust, Nottingham.

Insights

Granulocyte colony-stimulating factor (G-CSF) influences polymorphonuclear leucocyte (PMN) function in end-stage renal failure (ESRF) patients on dialysis. While G-CSF did not correct all PMN abnormalities, it appears safe for ESRF patients.

Area of Science:

  • Nephrology
  • Immunology
  • Hematology

Background:

  • End-stage renal failure (ESRF) patients on continuous ambulatory peritoneal dialysis (CAPD) are immunocompromised.
  • These patients exhibit abnormal polymorphonuclear leucocyte (PMN) function, including reduced phagocytosis and intracellular killing.
  • Understanding the impact of therapeutic interventions on PMN function in ESRF is crucial for patient management.

Purpose of the Study:

  • To investigate the effects of granulocyte colony-stimulating factor (G-CSF) on PMN function in ESRF patients undergoing CAPD.
  • To assess the safety and efficacy of G-CSF in modulating specific PMN functional parameters.

Main Methods:

  • Six ESRF patients on CAPD received daily 300 microg G-CSF for 5 days.
  • PMN function tests were conducted daily, including assessments of CD11b and L-selectin (CD62L) expression, superoxide anion production, and Fc gamma receptor (Fc gammaRI/CD64, Fc gammaRII/CD16) expression.
  • Circulating white cell and PMN counts were monitored.

Main Results:

  • G-CSF treatment led to a significant decrease in CD11b expression and L-selectin (CD62L) expression in response to stimulation.
  • Superoxide anion production and Fc gammaRI (CD64) expression were significantly increased, while Fc gammaRII (CD16) expression was decreased.
  • Circulating white cell and PMN counts were significantly elevated; however, phagocytosis and intracellular killing abnormalities were not corrected.

Conclusions:

  • G-CSF influences uraemic PMN function in ESRF patients, with effects comparable to those observed in non-uraemic subjects.
  • G-CSF administration did not appear to cause harm to ESRF patients.
  • Further research is needed to fully elucidate the therapeutic potential of G-CSF in managing immune dysfunction in ESRF patients.

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