Previous Article | Next Article ![]()
Antimicrobial Agents and Chemotherapy, October 2006, p. 3444-3446, Vol. 50, No. 10
0066-4804/06/$08.00+0 doi:10.1128/AAC.00372-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Rega Institute for Medical Research, KULeuven, 3000 Leuven, Belgium,1 Department of Molecular Virology, University of Heidelberg, 69120 Heidelberg, Germany2
Received 27 March 2006/ Returned for modification 8 May 2006/ Accepted 31 July 2006
Ribavirin antagonizes the in vitro anti-hepatitis C virus (HCV) activity of the pyrimidine nucleoside analogue 2'-C-methylcytidine, the active component of the experimental anti-HCV drug valopicitabine. In contrast, the combination of ribavirin with either the purine nucleoside analogue 2'-C-methyladenosine or the HCV protease inhibitor VX-950 resulted in an additive antiviral activity. These findings may have implications when planning clinical studies with valopicitabine.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»