Thromb Haemost 2005; 93(06): 1036-1040
DOI: 10.1160/TH04-08-0492
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Activation of coagulation and inhibition of fibrinolysis in the lung after inhalation of lipopolysaccharide by healthy volunteers

Nico A. Maris
1   Departments of Experimental Internal Medicine
,
Alex F. de Vos
1   Departments of Experimental Internal Medicine
,
Paul Bresser
2   Pulmonology, Tropical Medicine and AIDS, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
,
Jaring S. van der Zee
2   Pulmonology, Tropical Medicine and AIDS, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
,
Joost C. Meijers
3   Vascular Medicine, Tropical Medicine and AIDS, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
,
Roger H. Lijnen
4   Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium
,
Marcel Levi
3   Vascular Medicine, Tropical Medicine and AIDS, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
5   Internal Medicine, Tropical Medicine and AIDS, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
,
Henk M. Jansen
2   Pulmonology, Tropical Medicine and AIDS, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
,
Tom van der Poll
1   Departments of Experimental Internal Medicine
6   Infectious Diseases, Tropical Medicine and AIDS, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
› Author Affiliations

Financial support: This work was supported by a grant from the Dutch Asthma Foundation (project 329909) to N. A. Maris.
Further Information

Publication History

Received 11 August 2004

Accepted after resubmission 15 March 2005

Publication Date:
11 December 2017 (online)

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Summary

Pneumonia is frequently associated with changes in coagulation and fibrinolysis in the bronchoalveolar space. To determine the effect of lipopolysaccharide (LPS) on the hemostatic balance in the human lung, six healthy subjects inhaled nebulized LPS or saline in a randomized cross-over study and bronchoalveolar lavage fluid was obtained six hours thereafter. LPS induced soluble tissue factor and thrombin-antithrombin complexes and inhibited plasminogen activator activity in BALF. Additionally plasminogen activator inhibitor type 1 production was upregulated after LPS inhalation. LPS also elicited local activation of neutrophils (release of elastase, myeloperoxidase and bactericidal/permeability increasing protein) and secretion of interleukin (IL)-6 and IL-8. Inhalation of LPS by healthy humans reproduces major features of the procoagulant response to inflammatory and infectious lung diseases and may be used as a novel model to evaluate pathogenetic mechanisms and new interventions.