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Antimicrobial Agents and Chemotherapy, August 2007, p. 2965-2968, Vol. 51, No. 8
0066-4804/07/$08.00+0 doi:10.1128/AAC.00219-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Lisa Alleva,1,
Mohammed Alsharifi,2
Aulikki Koskinen,2
Victoria Smythe,2
Arno Müllbacher,2
Jeff Wood,3 and
Ian Clark1*
School of Biochemistry and Molecular Biology,1 John Curtin School of Medical Research,2 Statistical Consulting Unit, Australian National University, Canberra ACT 0200, Australia3
Received 13 February 2007/ Returned for modification 29 March 2007/ Accepted 24 May 2007
Gemfibrozil, 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.
Published ahead of print on 11 June 2007.
A.B. and L.A. contributed equally to this study.
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