Gastroenterology

Gastroenterology

Volume 150, Issue 1, January 2016, Pages 82-85.e4
Gastroenterology

Original Research
Brief Report
Sofosbuvir Inhibits Hepatitis E Virus Replication In Vitro and Results in an Additive Effect When Combined With Ribavirin

https://doi.org/10.1053/j.gastro.2015.09.011Get rights and content

Infection with hepatitis E virus genotype 3 may result in chronic hepatitis in immunocompromised patients. Reduction of immunosuppression or treatment with ribavirin or pegylated interferon-α can result in viral clearance. However, safer and more effective treatment options are needed. Here, we show that sofosbuvir inhibits the replication of hepatitis E virus genotype 3 both in subgenomic replicon systems as well as a full-length infectious clone. Moreover, the combination of sofosbuvir and ribavirin results in an additive antiviral effect. Sofosbuvir may be considered as an add-on therapy to ribavirin for the treatment of chronic hepatitis E in immunocompromised patients.

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Acknowledgments

The authors gratefully acknowledge Suzanne U. Emerson for sharing reagents as well as William E. Delaney and Adrian Ray for sharing unpublished data.

References (15)

  • N. Kamar

    Lancet

    (2012)
  • Y. Debing

    Antiviral Res

    (2014)
  • J.M. Pawlotsky

    Gastroenterology

    (2014)
  • S.S. Carroll

    J Biol Chem

    (2003)
  • F.G. Bahar

    J Pharm Sci

    (2012)
  • J.H. Hoofnagle

    N Engl J Med

    (2012)
  • N. Kamar

    N Engl J Med

    (2014)
There are more references available in the full text version of this article.

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Conflicts of interest The authors disclose no conflicts.

Funding This work was supported by grants 31003A-138484 and 31003A-156030 from the Swiss National Science Foundation (D.M.); the Interuniversity Attraction Poles Programme of the Belgian Federal Science Policy Office and the KU Leuven Geconcerteerde Onderzoeksacties (J.N.); and the Starr Foundation, as well as anonymous donors (C.M.R.). Also supported by a postdoctoral fellowship from the Deutsche Forschungsgemeinschaft (V.L.D.T.), a pilot grant from the Robertson Foundation (V.L.D.T. and C.M.R.), a fellowship from the Research Foundation Flanders (Y.D.), and a postdoctoral fellowship from Bristol-Myers Squibb at The Rockefeller University (X.W.).

Author names in bold designate shared co-first authorship.

§

Authors share co-senior authorship.

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