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School of Biochemistry and Molecular Biology, John Curtin School of Medical Research, and Statistical Consulting Unit, Australian National University, Canberra, ACT 0200, Australia
* To whom correspondence should be addressed. Email: ian.clark{at}anu.edu.au.
| Abstract |
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Gemfibrozil, an agent that inhibits production of pro-inflammatory 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 administered 60 mg/kg/day gemfibrozil (n=46) (p=0.0026). If this principle translates across to patients, a drug already approved for human use, albeit by a different route for another purpose, might be relatively fast to adapt for use against influenza disease, conceivably including human infection by a derivative of the avian H5N1 strain.
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