Factor V Leiden mutation does not affect coagulopathy or outcome in lethal H1N1 influenza

Influenza A is a major cause of mortality. Knowledge on coagulation activation in influenza infection is limited. The factor V Leiden (FVL) mutation is possibly subject to positive selection pressure. It is unknown whether this mutation impacts on the outcome of severe influenza. In the present stud...

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Veröffentlicht in:The European respiratory journal 2010-12, Vol.36 (6), p.1346-1354
Hauptverfasser: SCHOUTEN, M, VAN DER SLUIJS, K. F, ROELOFS, J. J. T. H, LEVI, M, VAN'T VEER, C, VAN DER POLL, T
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container_issue 6
container_start_page 1346
container_title The European respiratory journal
container_volume 36
creator SCHOUTEN, M
VAN DER SLUIJS, K. F
ROELOFS, J. J. T. H
LEVI, M
VAN'T VEER, C
VAN DER POLL, T
description Influenza A is a major cause of mortality. Knowledge on coagulation activation in influenza infection is limited. The factor V Leiden (FVL) mutation is possibly subject to positive selection pressure. It is unknown whether this mutation impacts on the outcome of severe influenza. In the present study, the effect of lethal influenza on pulmonary and systemic coagulation activation and whether or not FVL mutation alters coagulation activation in and the course of lethal influenza, was determined. Wild-type mice, and mice heterozygous or homozygous for FVL were infected intranasally with a lethal dose of H1N1 (haemagglutinin 1 and neuraminidase 1) influenza A. Mice were sacrificed after 48 or 96 h for determination of coagulation activation, histopathology, pulmonary inflammatory parameters and viral load, or were observed in a survival study. Extensive local and systemic coagulation activation during lethal influenza was demonstrated by increased lung and plasma levels of thrombin-antithrombin complexes and fibrin degradation products, and by pulmonary fibrin deposition. FVL mutation did not influence the procoagulant response, lung histopathology or survival. FVL mice demonstrated elevated viral loads 48 h after infection. In conclusion, coagulation is activated locally and systemically during lethal murine influenza A infection. The FVL mutation does not influence coagulation activation, lung inflammation or survival in lethal influenza A.
doi_str_mv 10.1183/09031936.00204909
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Mice were sacrificed after 48 or 96 h for determination of coagulation activation, histopathology, pulmonary inflammatory parameters and viral load, or were observed in a survival study. Extensive local and systemic coagulation activation during lethal influenza was demonstrated by increased lung and plasma levels of thrombin-antithrombin complexes and fibrin degradation products, and by pulmonary fibrin deposition. FVL mutation did not influence the procoagulant response, lung histopathology or survival. FVL mice demonstrated elevated viral loads 48 h after infection. In conclusion, coagulation is activated locally and systemically during lethal murine influenza A infection. 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subjects Animals
Antithrombins - analysis
Biological and medical sciences
Blood Coagulation Disorders - genetics
Blood Coagulation Factors - analysis
Factor V - genetics
Female
Fibrin Fibrinogen Degradation Products - analysis
Hematologic and hematopoietic diseases
Heterozygote
Homozygote
Human viral diseases
Infectious diseases
Influenza A Virus, H1N1 Subtype
Lung - metabolism
Lung - pathology
Male
Medical sciences
Mice
Mice, Inbred C57BL
Orthomyxoviridae Infections - blood
Orthomyxoviridae Infections - mortality
Platelet diseases and coagulopathies
Pneumology
Point Mutation
Severity of Illness Index
Thrombin - analysis
Viral diseases
Viral diseases of the respiratory system and ent viral diseases
Viral Load
title Factor V Leiden mutation does not affect coagulopathy or outcome in lethal H1N1 influenza
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