| Literature DB >> 17576833 |
Joanna Chapman1, Elizabeth Abbott, Dagmar G Alber, Robert C Baxter, Sian K Bithell, Elisa A Henderson, Malcolm C Carter, Phil Chambers, Ann Chubb, G Stuart Cockerill, Peter L Collins, Verity C L Dowdell, Sally J Keegan, Richard D Kelsey, Michael J Lockyer, Cindy Luongo, Pilar Najarro, Raymond J Pickles, Mark Simmonds, Debbie Taylor, Stan Tyms, Lara J Wilson, Kenneth L Powell.
Abstract
Respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract infections worldwide, yet no effective vaccine or antiviral treatment is available. Here we report the discovery and initial development of RSV604, a novel benzodiazepine with submicromolar anti-RSV activity. It proved to be equipotent against all clinical isolates tested of both the A and B subtypes of the virus. The compound has a low rate of in vitro resistance development. Sequencing revealed that the resistant virus had mutations within the nucleocapsid protein. This is a novel mechanism of action for anti-RSV compounds. In a three-dimensional human airway epithelial cell model, RSV604 was able to pass from the basolateral side of the epithelium effectively to inhibit virus replication after mucosal inoculation. RSV604, which is currently in phase II clinical trials, represents the first in a new class of RSV inhibitors and may have significant potential for the effective treatment of RSV disease.Entities:
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Year: 2007 PMID: 17576833 PMCID: PMC2043207 DOI: 10.1128/AAC.00211-07
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191