| Literature DB >> 18008229 |
Jessica A Belser1, Xiuhua Lu, Kristy J Szretter, Xiaoping Jin, Laura M Aschenbrenner, Alice Lee, Stephen Hawley, Do Hyong Kim, Michael P Malakhov, Mang Yu, Fang Fang, Jacqueline M Katz.
Abstract
Increasing resistance to currently available influenza antivirals highlights the need to develop alternate approaches for the prevention and/or treatment of influenza. DAS181 (Fludase), a novel sialidase fusion protein that enzymatically removes sialic acids on respiratory epithelium, exhibits potent antiviral activity against influenza A and B viruses. Here, we use a mouse model to evaluate the efficacy of DAS181 treatment against a highly pathogenic avian influenza H5N1 virus. When used to treat mice daily beginning 1 day before infection with A/Vietnam/1203/2004(H5N1) virus, DAS181 treatment at 1 mg/kg/day protected 100% of mice from fatal disease, prevented viral dissemination to the brain, and effectively blocked infection in 70% of mice. DAS181 at 1 mg/kg/day was also effective therapeutically, conferring enhanced survival of H5N1 virus-challenged mice when treatment was begun 72 h after infection. This notable antiviral activity underscores the potential utility of DAS181 as a new class of drug that is effective against influenza viruses with pandemic potential.Entities:
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Year: 2007 PMID: 18008229 DOI: 10.1086/522609
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226