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Clinical Trial
. 2004 Jan;239(1):75-81.
doi: 10.1097/01.sla.0000103062.21049.82.

Perioperative recombinant human granulocyte colony-stimulating factor (Filgrastim) treatment prevents immunoinflammatory dysfunction associated with major surgery

Affiliations
Clinical Trial

Perioperative recombinant human granulocyte colony-stimulating factor (Filgrastim) treatment prevents immunoinflammatory dysfunction associated with major surgery

Christian Schneider et al. Ann Surg. 2004 Jan.

Abstract

Objective: To examine the effects of perioperative rhG-CSF administration on immune function in patients subjected to major surgery.

Summary background data: Severe trauma, such as major surgery, initiates acute immunodysfunction which predisposes the patient towards infectious complications.

Methods: Sixty patients undergoing elective surgery received either recombinant human granulocyte colony-stimulating factor/rh G-CSF (Filgrastim) or a placebo perioperatively. At several time points before and after the surgical intervention immunofunctional parameters were assessed. RESULTS Leukocyte counts and serum levels of anti-inflammatory mediators (IL-1ra and TNF-R) were increased in Filgrastim-treated patients, while the post-operative acute phase response was attenuated. Monocyte deactivation (reduced TNF-alpha release and HLA-DR expression) and lymphocyte anergy (impaired mitogenic proliferation and reduced TH1 lymphokine release) were blunted and the incidence and severity of infectious complications were reduced.

Conclusions: These results suggest that Filgrastim treatment reinforces innate immunity, enabling better prevention of infection. Thus, this unique combination of hematopoietic, anti-inflammatory and anti-infectious effects on the innate immune system warrants further study of clinical efficacy and sepsis prophylaxis.

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Figures

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FIGURE 1. The experimental protocol of the study is depicted. Patients in the treatment group received rh G-CSF (15 μg/kg body weight) over 6 perioperative days either as 3 bolus administrations of 5 μg/kg body weight or as a continuous administration of 2 μg/kg body weight following an initial bolus of 5 μg/kg body weight.
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FIGURE 2. Perioperative Filgrastim treatment blunts trauma-induced acute phase reaction. Patients received placebo (empty bars) or Filgrastim (black bars) perioperatively. Total leukocyte counts (a), C-reactive protein (b) and G-CSF (c) serum concentrations are shown as means ± SEM *P ≤ 0.05; **P ≤ 0.001, relative to placebo values.
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FIGURE 3. Perioperative Filgrastim treatment blunts trauma-induced monocyte deactivation. Patients received placebo (empty bars) or Filgrastim (black bars) perioperatively. a: HLA-DR expression on monocytes. LPS-induced TNF-α (b), IL-6 (c), and IL-1ra (d) release in diluted whole blood. Data represent means ± SEM. *P ≤ 0.05; **P ≤ 0.001, relative to placebo values.

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