Literature DB >> 3804202

Effects of adenine arabinoside on serum and intrahepatic replicative forms of duck hepatitis B virus in chronic infection.

K Hirota, A H Sherker, M Omata, O Yokosuka, K Okuda.   

Abstract

Adenine arabinoside is an antiviral agent which has been used in a number of clinical studies for the treatment of chronic infections with hepatitis B virus. In order to better understand its effects and mode of action, we treated ducks chronically infected with duck hepatitis B virus with a 2-week course and monitored the effects of the drug on viral replication by studying duck hepatitis B virus DNA in liver and serum using molecular biological techniques. We found the drug to be effective in ducks only at much higher doses than those used in humans. At high doses, adenine arabinoside had a dose-related inhibitory effect on viral replication during treatment, but there was a rapid return toward baseline values soon after the cessation of treatment. The supercoiled form of viral DNA was found to be most resistant to adenine arabinoside therapy, and the drug had a disproportionate inhibitory effect on viral plus (noncoding) strand synthesis. We conclude that adenine arabinoside likely exerts its effect in hepadna virus infections predominantly through inhibition of viral DNA polymerase. On the basis of our current study and previous trials in hepatitis B virus-infected patients, we predict that adenine arabinoside will not efficiently eliminate viral replication in chronic hepadna virus infection, when used as the sole therapeutic modality. Adenine arabinoside may have a role to play as an adjunct to immunomodulation or interferon therapy in chronic hepatitis B virus infection in man.

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Year:  1987        PMID: 3804202     DOI: 10.1002/hep.1840070107

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  8 in total

1.  Sulfated polyanions do not inhibit duck hepatitis B virus infection.

Authors:  W B Offensperger; S Offensperger; E Walter; H E Blum; W Gerok
Journal:  Antimicrob Agents Chemother       Date:  1991-11       Impact factor: 5.191

2.  Inhibition of duck hepatitis B virus DNA replication by antiviral chemotherapy with ganciclovir-nalidixic acid.

Authors:  Y Wang; C Luscombe; S Bowden; T Shaw; S Locarnini
Journal:  Antimicrob Agents Chemother       Date:  1995-02       Impact factor: 5.191

3.  In vitro antiviral activity of penciclovir, a novel purine nucleoside, against duck hepatitis B virus.

Authors:  T Shaw; P Amor; G Civitico; M Boyd; S Locarnini
Journal:  Antimicrob Agents Chemother       Date:  1994-04       Impact factor: 5.191

4.  Inhibitory effects of 2'-fluorinated arabinosyl-pyrimidine nucleosides on woodchuck hepatitis virus replication in chronically infected woodchucks.

Authors:  I Fourel; O Hantz; K A Watanabe; C Jacquet; B Chomel; J J Fox; C Trepo
Journal:  Antimicrob Agents Chemother       Date:  1990-03       Impact factor: 5.191

5.  Effects of antiviral agents on chronic hepatitis B. Analysis using Cox proportional hazard model.

Authors:  S Takano; M Omata; O Yokosuka; F Imazeki; M Ohto
Journal:  Dig Dis Sci       Date:  1992-11       Impact factor: 3.199

6.  Antisense therapy of hepatitis B virus infection.

Authors:  W B Offensperger; S Offensperger; H E Blum
Journal:  Mol Biotechnol       Date:  1998-04       Impact factor: 2.695

7.  Evaluation of the potent anti-hepatitis B virus agent (-) cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]cytosine in a novel in vivo model.

Authors:  L D Condreay; R W Jansen; T F Powdrill; L C Johnson; D W Selleseth; M T Paff; S M Daluge; G R Painter; P A Furman; M N Ellis
Journal:  Antimicrob Agents Chemother       Date:  1994-03       Impact factor: 5.191

8.  Inhibition of intrahepatic hepatitis B virus replication by antiviral drugs in a novel transgenic mouse model.

Authors:  T Nagahata; K Araki; K Yamamura; K Matsubara
Journal:  Antimicrob Agents Chemother       Date:  1992-09       Impact factor: 5.191

  8 in total

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