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Journal of Clinical Microbiology, December 2004, p. 5861-5865, Vol. 42, No. 12
0095-1137/04/$08.00+0 DOI: 10.1128/JCM.42.12.5861-5865.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
INSERM U526-IFR 50, Laboratoire de Virologie, Faculté de Médecine, Nice, France
Received 18 December 2003/ Returned for modification 15 March 2004/ Accepted 25 June 2004
Human HepG2 hepatoma cells are highly permissive for influenza virus type A and type B, even without the addition of trypsin, and they exhibit a marked cytopathic effect. This property greatly facilitates the primary isolation of influenza viruses. Virus replication was significantly reduced by the plasmin(ogen)-specific inhibitor tranexamic acid, and this suggests a potential role played by the plasminogen/tissue plasminogen activator complex at the surface of HepG2 cells. This might represent a new approach for study of the interrelations of this complex with influenza viruses.
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