Abstract
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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 374-382 |
| Number of pages | 9 |
| Journal | The Lancet Infectious Diseases |
| Volume | 5 |
| Issue number | 6 |
| DOIs | |
| State | Published - Jun 2005 |
ASJC Scopus subject areas
- Infectious Diseases
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