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Increased survival after gemfibrozil treatment of severe mouse influenza

dc.contributor.authorBudd, Alison
dc.contributor.authorAlleva, Lisa
dc.contributor.authorAlsharifi, Mohammed
dc.contributor.authorKoskinen, Aulikki
dc.contributor.authorSmythe, Victoria
dc.contributor.authorMullbacher, Arno
dc.contributor.authorWood, Jeffrey
dc.contributor.authorClark, Ian A
dc.date.accessioned2015-12-08T22:20:17Z
dc.date.issued2007
dc.date.updated2015-12-08T08:29:21Z
dc.description.abstractGemfibrozil, an agent that inhibits production of proinflammatory cytokines in addition to its clinically useful lipid-lowering activity, increased survival in BALB/c mice that were already ill from infection by influenza virus A/Japan/305/57 (H2N2). Gemfibrozil was administered intraperitoneally once daily from days 4 to 10 after intranasal exposure to the virus. Survival increased from 26% in vehicle-treated mice (n = 50) to 52% in mice given gemfibrozil at 60 mg/kg/day (n = 46) (P = 0.0026). If this principle translates to patients, a drug already approved for human use, albeit by a different route for another purpose, might be adapted relatively fast for use against influenza, conceivably including human infection with a derivative of the avian H5N1 strain.
dc.identifier.issn0066-4804
dc.identifier.urihttp://hdl.handle.net/1885/31927
dc.publisherAmerican Society for Microbiology
dc.sourceAntimicrobial Agents and Chemotherapy
dc.subjectKeywords: cytokine; gemfibrozil; adolescent; animal experiment; animal model; article; Bagg albino mouse; controlled study; cytokine production; drug efficacy; female; influenza; Influenza virus A; Influenza virus A H5N1; mouse; nonhuman; priority journal; survival
dc.titleIncreased survival after gemfibrozil treatment of severe mouse influenza
dc.typeJournal article
local.bibliographicCitation.issue8
local.bibliographicCitation.lastpage2968
local.bibliographicCitation.startpage2965
local.contributor.affiliationBudd, Alison, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationAlleva, Lisa, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationAlsharifi, Mohammed, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationKoskinen, Aulikki, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationSmythe, Victoria, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationMullbacher, Arno, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationWood, Jeffrey, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationClark, Ian A, College of Medicine, Biology and Environment, ANU
local.contributor.authoruidBudd, Alison, u4005132
local.contributor.authoruidAlleva, Lisa, u9306857
local.contributor.authoruidAlsharifi, Mohammed, a265709
local.contributor.authoruidKoskinen, Aulikki, u9108883
local.contributor.authoruidSmythe, Victoria, u4255220
local.contributor.authoruidMullbacher, Arno, u8102295
local.contributor.authoruidWood, Jeffrey, u4039956
local.contributor.authoruidClark, Ian A, a261318
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor111502 - Clinical Pharmacology and Therapeutics
local.identifier.ariespublicationu4325460xPUB87
local.identifier.citationvolume51
local.identifier.doi10.1128/AAC.00219-07
local.identifier.scopusID2-s2.0-34547638447
local.type.statusPublished Version

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