Literature DB >> 10722482

Broad-spectrum antiviral activity of the IMP dehydrogenase inhibitor VX-497: a comparison with ribavirin and demonstration of antiviral additivity with alpha interferon.

W Markland1, T J McQuaid, J Jain, A D Kwong.   

Abstract

The enzyme IMP dehydrogenase (IMPDH) catalyzes an essential step in the de novo biosynthesis of guanine nucleotides, namely, the conversion of IMP to XMP. The major event occurring in cells exposed to competitive IMPDH inhibitors such as ribavirin or uncompetitive inhibitors such as mycophenolic acid (MPA) is a depletion of the intracellular GTP and dGTP pools. Ribavirin is approved as an inhaled antiviral agent for treatment of respiratory syncytial virus (RSV) infection and orally, in combination with alpha interferon (IFN-alpha), for the treatment of chronic hepatitis C virus (HCV) infection. VX-497 is a potent, reversible uncompetitive IMPDH inhibitor which is structurally unrelated to other known IMPDH inhibitors. Studies were performed to compare VX-497 and ribavirin in terms of their cytotoxicities and their efficacies against a variety of viruses. They included DNA viruses (hepatitis B virus [HBV], human cytomegalovirus [HCMV], and herpes simplex virus type 1 [HSV-1]) and RNA viruses (respiratory syncytial virus [RSV], parainfluenza-3 virus, bovine viral diarrhea virus, Venezuelan equine encephalomyelitis virus [VEEV], dengue virus, yellow fever virus, coxsackie B3 virus, encephalomyocarditis virus [EMCV], and influenza A virus). VX-497 was 17- to 186-fold more potent than ribavirin against HBV, HCMV, RSV, HSV-1, parainfluenza-3 virus, EMCV, and VEEV infections in cultured cells. The therapeutic index of VX-497 was significantly better than that of ribavirin for HBV and HCMV (14- and 39-fold, respectively). Finally, the antiviral effect of VX-497 in combination with IFN-alpha was compared to that of ribavirin with IFN-alpha in the EMCV replication system. Both VX-497 and ribavirin demonstrated additivity when coapplied with IFN-alpha, with VX-497 again being the more potent in this combination. These data are supportive of the hypothesis that VX-497, like ribavirin, is a broad-spectrum antiviral agent.

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Year:  2000        PMID: 10722482      PMCID: PMC89783          DOI: 10.1128/AAC.44.4.859-866.2000

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  31 in total

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Review 3.  Biochemistry and clinical applications of ribavirin.

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Journal:  Antimicrob Agents Chemother       Date:  1986-08       Impact factor: 5.191

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Journal:  Science       Date:  1972-08-25       Impact factor: 47.728

5.  Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei.

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Journal:  Nucleic Acids Res       Date:  1983-03-11       Impact factor: 16.971

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Authors:  A C Allison; T Hovi; R W Watts; A D Webster
Journal:  Ciba Found Symp       Date:  1977

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Authors:  S K Wray; B E Gilbert; M W Noall; V Knight
Journal:  Antiviral Res       Date:  1985-02       Impact factor: 5.970

8.  Effect of ribavirin triphosphate on primer generation and elongation during influenza virus transcription in vitro.

Authors:  S K Wray; B E Gilbert; V Knight
Journal:  Antiviral Res       Date:  1985-02       Impact factor: 5.970

9.  Effect of phosphorylated ribavirin on vesicular stomatitis virus transcription.

Authors:  P Toltzis; K O'Connell; J L Patterson
Journal:  Antimicrob Agents Chemother       Date:  1988-04       Impact factor: 5.191

10.  Use of a standardized cell culture assay to assess activities of nucleoside analogs against hepatitis B virus replication.

Authors:  B E Korba; J L Gerin
Journal:  Antiviral Res       Date:  1992-07-01       Impact factor: 5.970

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2.  Synergistic in vitro interactions between alpha interferon and ribavirin against bovine viral diarrhea virus and yellow fever virus as surrogate models of hepatitis C virus replication.

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Review 5.  Anti-rods/rings autoantibody generation in hepatitis C patients during interferon-α/ribavirin therapy.

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Review 6.  The application and mechanism of action of ribavirin in therapy of hepatitis C.

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Journal:  Antivir Chem Chemother       Date:  2012-09-25

Review 7.  IMP dehydrogenase: structure, mechanism, and inhibition.

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10.  Analysis of ribavirin mutagenicity in human hepatitis C virus infection.

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Journal:  J Virol       Date:  2007-05-09       Impact factor: 5.103

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