| Literature DB >> 12508146 |
Annelies Verbon1, Joost C M Meijers, C Arnold Spek, C Erik Hack, John P Pribble, Terence Turner, Pascale E P Dekkers, Tim Axtelle, Marcel Levi, Sander J H van Deventer, Pieter H Reitsma, Tom van der Poll.
Abstract
To determine the role of CD14 in lipopolysaccharide (LPS)-induced effects on coagulation and fibrinolysis in humans, 16 healthy subjects received an intravenous injection of LPS preceded by intravenous IC14, a recombinant chimeric monoclonal antibody against human CD14, or placebo. LPS-induced coagulation activation (tissue-factor mRNA in whole blood cells and plasma concentrations of F1+2) was not influenced by IC14, whereas the antibody reduced the increase in thrombin-antithrombin complexes and soluble fibrin. LPS injection also was associated with an early activation of fibrinolysis (plasma concentrations of tissue-type plasminogen activator and plasmin-alpha(2)-antiplasmin complexes), followed by an inhibitory response (plasminogen activator inhibitor type 1), which were attenuated by IC14. Furthermore, LPS reduced thrombin-activatable fibrinolysis-inhibitor antigen levels and increased soluble thrombomodulin levels, which were not influenced by IC14. These results suggest that different hemostatic responses during endotoxemia may proceed via CD14-dependent and -independent pathways.Entities:
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Year: 2002 PMID: 12508146 DOI: 10.1086/346043
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226