Literature DB >> 18441341

Why are there different dynamics in the selection of drug resistance in HIV and hepatitis B and C viruses?

Vincent Soriano1, Alan S Perelson, Fabien Zoulim.   

Abstract

The arrival of new antiviral drugs to treat chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infections has given rise to great expectations along with concerns regarding the selection of drug-resistant variants. Many lessons learnt from HIV therapeutics can be helpful for designing adequate treatment strategies against viral hepatitis, the avoidance of sequential weak monotherapies being one of them. Although HIV, HBV and HCV share many biological features, including very rapid viral dynamics, distinctive characteristics explain why the speed of selection of drug resistance differs substantially between these viruses, being faster for HCV than for HIV and slower for HBV.

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Year:  2008        PMID: 18441341      PMCID: PMC2574594          DOI: 10.1093/jac/dkn175

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  31 in total

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Journal:  Science       Date:  1998-10-02       Impact factor: 47.728

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Journal:  J Virol       Date:  1997-12       Impact factor: 5.103

5.  Biphasic clearance kinetics of hepatitis B virus from patients during adefovir dipivoxil therapy.

Authors:  M Tsiang; J F Rooney; J J Toole; C S Gibbs
Journal:  Hepatology       Date:  1999-06       Impact factor: 17.425

6.  Rapid in vitro selection of human immunodeficiency virus type 1 resistant to 3'-thiacytidine inhibitors due to a mutation in the YMDD region of reverse transcriptase.

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7.  Persistence of cccDNA during the natural history of chronic hepatitis B and decline during adefovir dipivoxil therapy.

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Journal:  Gastroenterology       Date:  2004-06       Impact factor: 22.682

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10.  Long-term follow-up of HIV-infected patients with chronic hepatitis C virus infection treated with interferon-based therapies.

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  23 in total

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Journal:  Nat Rev Gastroenterol Hepatol       Date:  2011-07-04       Impact factor: 46.802

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5.  Modeling quasispecies and drug resistance in hepatitis C patients treated with a protease inhibitor.

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9.  Virologic and serologic outcomes of mono versus dual HBV therapy and characterization of HIV/HBV coinfection in a US cohort.

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10.  Identification of HCV protease inhibitor resistance mutations by selection pressure-based method.

Authors:  Ping Qiu; Vincent Sanfiorenzo; Stephanie Curry; Zhuyan Guo; Shaotang Liu; Angela Skelton; Ellen Xia; Constance Cullen; Robert Ralston; Jonathan Greene; Xiao Tong
Journal:  Nucleic Acids Res       Date:  2009-04-24       Impact factor: 16.971

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