TY - JOUR
T1 - Management of patients co-infected with hepatitis B virus and HIV
AU - Núñez, Marina
AU - Soriano, Vincent
PY - 2005/6
Y1 - 2005/6
N2 - The management of chronic hepatitis B virus (HBV) infection poses specific problems in the presence of HIV co-infection, since therapeutic approaches have to consider both HBV and HIV infections. There are currently four drugs approved for the treatment of chronic HBV infection (interferon α, lamivudine, adefovir, and entecavir); the dual antiviral activity of tenofovir and emtricitabine broadens the armamentarium against HBV in HBV/HIV co-infected patients. Nucleotide analogues - eg, adefovir and tenofovir - have the advantage of a higher genetic barrier to the development of resistance compared with nucleoside analogues - eg, lamivudine and emtricitabine. Fortunately, the two families do not share resistance mutations, allowing salvage therapy and the possibility of combination therapy for drug-naive individuals. Although response to interferon α is poorer in HBV/HIV co-infected patients compared with HIV-negative individuals, especially in hepatitis B e antigen-negative HBV infection, the more potent pegylated forms of interferon α have brought new hope.
AB - The management of chronic hepatitis B virus (HBV) infection poses specific problems in the presence of HIV co-infection, since therapeutic approaches have to consider both HBV and HIV infections. There are currently four drugs approved for the treatment of chronic HBV infection (interferon α, lamivudine, adefovir, and entecavir); the dual antiviral activity of tenofovir and emtricitabine broadens the armamentarium against HBV in HBV/HIV co-infected patients. Nucleotide analogues - eg, adefovir and tenofovir - have the advantage of a higher genetic barrier to the development of resistance compared with nucleoside analogues - eg, lamivudine and emtricitabine. Fortunately, the two families do not share resistance mutations, allowing salvage therapy and the possibility of combination therapy for drug-naive individuals. Although response to interferon α is poorer in HBV/HIV co-infected patients compared with HIV-negative individuals, especially in hepatitis B e antigen-negative HBV infection, the more potent pegylated forms of interferon α have brought new hope.
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U2 - 10.1016/S1473-3099(05)70141-9
DO - 10.1016/S1473-3099(05)70141-9
M3 - Review article
C2 - 15919623
AN - SCOPUS:20344383740
SN - 1473-3099
VL - 5
SP - 374
EP - 382
JO - The Lancet Infectious Diseases
JF - The Lancet Infectious Diseases
IS - 6
ER -