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Entecavir Therapy Induces de Novo HIV Reverse‐Transcriptase M184V Mutation in an Antiretroviral Therapy–Naive Patient
Author(s) -
Martin R. Jakobsen,
Hanne Arildsen,
Henrik Krarup,
Martin Tolstrup,
Lars Østergaard,
Alex Lund Laursen
Publication year - 2008
Publication title -
clinical infectious diseases
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/587174
Subject(s) - entecavir , resistance mutation , medicine , lamivudine , virology , hepatitis b virus , population , reverse transcriptase , virus , hepatitis b , coinfection , immunology , biology , polymerase chain reaction , environmental health , gene , biochemistry
Recently, entecavir was introduced as a potent drug against hepatitis B virus infection. Initially, it was suggested not to have any effect on human immunodeficiency virus (HIV) infection. This guideline was revised in 2007 because of a report showing that the M184V mutation was selected in an hepatitis B virus and HIV-coinfected patient previously treated with lamivudine. Our investigation revealed findings similar to those preveiously reported but in an antiretroviral therapy-naive patient coinfected with HIV and hepatitis B virus. After 26 weeks of entecavir therapy, the M184V mutation dominated the plasma viral population. Thus, entecavir should only be used for coinfected patients who simultaneously receive suppressive therapy against HIV infection.

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