| Literature DB >> 26381519 |
J Daan de Boer1, Marieke Berger2, Christof J Majoor2, Liesbeth M Kager3, Joost C M Meijers4, Sanne Terpstra3, Rienk Nieuwland5, Anita N Boing5, René Lutter6, Diana Wouters7, Gerard J van Mierlo7, Sacha S Zeerleder8, Elisabeth H Bel9, Cornelis van't Veer3, Alex F de Vos3, Jaring S van der Zee10, Tom van der Poll11.
Abstract
Asthma patients show evidence of a procoagulant state in their airways, accompanied by an impaired function of the anticoagulant protein C system. We aimed to study the effect of recombinant human activated protein C (rhAPC) in allergic asthma patients.We conducted a randomised, double-blind, placebo-controlled, proof-of-concept study in house dust mite (HDM) allergic asthma patients. Patients were randomised to receive intravenous rhAPC (24 µg·kg(-1)·h(-1); n=12) or placebo (n=12) for 11 h. 4 h after the start of infusion, a first bronchoscopy was performed to challenge one lung segment with saline (control) and a contralateral segment with a combination of HDM extract and lipopolysaccharide (HDM+LPS), thereby mimicking environmental house dust exposure. A second bronchoscopy was conducted 8 h after intrabronchial challenge to obtain bronchoalveolar lavage fluid (BALF).rhAPC did not influence HDM+LPS induced procoagulant changes in the lung. In contrast, rhAPC reduced BALF leukocyte counts by 43% relative to placebo, caused by an inhibitory effect on neutrophil influx (64% reduction), while leaving eosinophil influx unaltered. rhAPC also reduced neutrophil degranulation products in the airways.Intravenous rhAPC attenuates HDM+LPS-induced neutrophil migration and protein release in allergic asthma patients by an effect that does not rely on coagulation inhibition.Entities:
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Year: 2015 PMID: 26381519 DOI: 10.1183/13993003.00459-2015
Source DB: PubMed Journal: Eur Respir J ISSN: 0903-1936 Impact factor: 16.671