Modeling host responses in ferrets during A/California/07/2009 influenza infection

Abstract Immune responses during infection with pandemic H1N1 2009 influenza A virus (2009-H1N1) are still poorly understood. Using an experimental infection model in ferrets, we examined the pathological features and characterized the host immune responses by using microarray analysis, during infec...

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Veröffentlicht in:Virology (New York, N.Y.) N.Y.), 2010-06, Vol.401 (2), p.257-265
Hauptverfasser: Rowe, Thomas, León, Alberto J, Crevar, Corey J, Carter, Donald M, Xu, Luoling, Ran, Longsi, Fang, Yuan, Cameron, Cheryl M, Cameron, Mark J, Banner, David, Ng, Derek C.K, Ran, Ran, Weirback, Heather K, Wiley, Clayton A, Kelvin, David J, Ross, Ted M
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Sprache:eng
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Zusammenfassung:Abstract Immune responses during infection with pandemic H1N1 2009 influenza A virus (2009-H1N1) are still poorly understood. Using an experimental infection model in ferrets, we examined the pathological features and characterized the host immune responses by using microarray analysis, during infection with 2009-H1N1 A/California/07/2009 and seasonal A/Brisbane/59/2007. Chemokines CCL2, CCL8, CXCL7 and CXCL10 along with the majority of interferon-stimulated genes were expressed early, correlated to lung pathology, and abruptly decreased expression on day 7 following infection of A/California/07/2009. Interestingly, the drop in innate immune gene expression was replaced by a significant increase of the adaptive immune genes for granzymes and immunoglobulins. Serum anti-influenza antibodies were first observed on day 7, commensurate with the viral clearance. We propose that lung pathology in humans occurs during the innate phase of host immunity and a delay or failure to switch to the adaptive phase may contribute to morbidity and mortality during severe 2009-H1N1 infections.
ISSN:0042-6822
1096-0341
DOI:10.1016/j.virol.2010.02.020