TY - JOUR
T1 - Complications in treating chronic hepatitis B in patients with HIV
AU - Soriano, Vincent
AU - Nuñez, Marina
AU - Sheldon, Julie
AU - Ramos, Belen
AU - Garcia-Samaniego, Javier
AU - Martín-Carbonero, Luz
AU - Maida, Ivana
AU - Gonzalez-Lahoz, Juan
PY - 2005/12
Y1 - 2005/12
N2 - The management of chronic hepatitis B virus (HBV) poses specific problems in the presence of HIV infection, as therapeutic approaches have to consider both HBV and HIV. There are currently four drugs approved for the treatment of chronic HBV. IFN-α, lamivudine, adefovir and entecavir. Furthermore, the dual antiviral activity against HIV and HBV of antiretrovirals such as tenofovir and emtricitabine broadens the armamentarium against HBV in the HIV-coinfected population. Nucleotide analogues adefovir and tenofovir have the advantage of a higher genetic barrier for resistance when compared with the nucleoside analogues lamivudine and emtricitabine. Fortunately, the two families do not share resistance mutations, allowing salvage therapy and the consideration of combination therapy for drug-naive individuals. Although response to IFN-α is poorer in HBV/HIV-coinfected patients compared with HBV-monoinfected individuals, the more potent pegylated forms of IFN-α have brought new hopes.
AB - The management of chronic hepatitis B virus (HBV) poses specific problems in the presence of HIV infection, as therapeutic approaches have to consider both HBV and HIV. There are currently four drugs approved for the treatment of chronic HBV. IFN-α, lamivudine, adefovir and entecavir. Furthermore, the dual antiviral activity against HIV and HBV of antiretrovirals such as tenofovir and emtricitabine broadens the armamentarium against HBV in the HIV-coinfected population. Nucleotide analogues adefovir and tenofovir have the advantage of a higher genetic barrier for resistance when compared with the nucleoside analogues lamivudine and emtricitabine. Fortunately, the two families do not share resistance mutations, allowing salvage therapy and the consideration of combination therapy for drug-naive individuals. Although response to IFN-α is poorer in HBV/HIV-coinfected patients compared with HBV-monoinfected individuals, the more potent pegylated forms of IFN-α have brought new hopes.
KW - Adefovir
KW - Emtricitabine
KW - Entecavir
KW - Hepatitis B
KW - HIV
KW - IFN
KW - Lamivudine
KW - Tenofovir
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U2 - 10.1517/14656566.6.16.2831
DO - 10.1517/14656566.6.16.2831
M3 - Review article
C2 - 16318434
AN - SCOPUS:29444446205
SN - 1465-6566
VL - 6
SP - 2831
EP - 2842
JO - Expert Opinion on Pharmacotherapy
JF - Expert Opinion on Pharmacotherapy
IS - 16
ER -