Tissue factor pathway inhibitor dose-dependently inhibits coagulation activation without influencing the fibrinolytic and cytokine response during human endotoxemia

Blood. 2000 Feb 15;95(4):1124-9.

Abstract

Inhibition of the tissue factor pathway has been shown to attenuate the activation of coagulation and to prevent death in a gram-negative bacteremia primate model of sepsis. It has been suggested that tissue factor influences inflammatory cascades other than the coagulation system. The authors sought to determine the effects of 2 different doses of recombinant tissue factor pathway inhibitor (TFPI) on endotoxin-induced coagulant, fibrinolytic, and cytokine responses in healthy humans. Two groups, each consisting of 8 healthy men, were studied in a double-blind, randomized, placebo-controlled crossover study. Subjects were studied on 2 different occasions. They received a bolus intravenous injection of 4 ng/kg endotoxin, which was followed by a 6-hour continuous infusion of TFPI or placebo. Eight subjects received 0.05 mg/kg per hour TFPI after a bolus of 0.0125 mg/kg (low-dose group), and 8 subjects received 0.2 mg/kg per hour after a bolus of 0.05 mg/kg (high-dose group). Endotoxin injection induced the activation of coagulation, the activation and subsequent inhibition of fibrinolysis, and the release of proinflammatory and antiinflammatory cytokines. TFPI infusion induced a dose-dependent attenuation of thrombin generation, as measured by plasma F1 + 2 and thrombin-antithrombin complexes, with a complete blockade of coagulation activation after high-dose TFPI. Endotoxin-induced changes in the fibrinolytic system and cytokine levels were not altered by either low-dose or high-dose TFPI. The authors concluded that TFPI effectively and dose-dependently attenuates the endotoxin-induced coagulation activation in humans without influencing the fibrinolytic and cytokine response. (Blood. 2000;95:1124-1129)

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Anticoagulants / administration & dosage
  • Anticoagulants / pharmacology*
  • Antithrombin III / metabolism
  • Blood Coagulation / drug effects*
  • Blood Pressure / drug effects
  • Body Temperature / drug effects
  • Cross-Over Studies
  • Cytokines / blood*
  • Double-Blind Method
  • Drug Administration Schedule
  • Endotoxemia / blood*
  • Endotoxemia / drug therapy
  • Endotoxemia / immunology
  • Escherichia coli Infections / blood
  • Escherichia coli Infections / drug therapy
  • Escherichia coli Infections / immunology
  • Fibrinolysis / drug effects
  • Heart Rate / drug effects
  • Humans
  • Infusions, Intravenous
  • Injections, Intravenous
  • Lipopolysaccharides / administration & dosage
  • Lipoproteins / administration & dosage
  • Lipoproteins / pharmacology*
  • Male
  • Peptide Hydrolases / metabolism
  • Plasminogen Activator Inhibitor 1 / blood

Substances

  • Anticoagulants
  • Cytokines
  • Lipopolysaccharides
  • Lipoproteins
  • Plasminogen Activator Inhibitor 1
  • antithrombin III-protease complex
  • lipoprotein-associated coagulation inhibitor
  • Antithrombin III
  • Peptide Hydrolases