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A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
Published on: May 10, 2022
Treatment algorithm for chronic hepatitis B in HIV-infected patients
1Hôpital Pitié-Salpêtrière, Service d'Hépato-Gastroentérologie, 27 boulevard de l'Hopital, 75013 Paris, France. ybenhamou@teaser.fr
Insights
Treating chronic hepatitis B (CHB) in HIV patients requires careful drug selection due to viral interactions. Tenofovir disoproxil fumarate (TDF) is recommended for patients with lamivudine-resistant hepatitis B virus (HBV).
Area of Science:
- Hepatology
- Infectious Diseases
- Antiviral Therapy
Background:
- Treatment of chronic hepatitis B (CHB) in HIV-infected patients is complex.
- Lack of controlled trials and dual activity of agents on both viruses complicate recommendations.
- Pragmatic approaches using data from HBV mono- and HIV/HBV co-infected studies are necessary.
Purpose of the Study:
- To provide pragmatic recommendations for optimal anti-HBV therapy in HIV-infected patients.
- To review approved CHB drugs and their efficacy/resistance profiles in co-infected individuals.
- To guide drug selection based on patient status (naive, requiring HIV therapy, HBV resistance).
Main Methods:
- Review of approved anti-CHB drugs: interferon alpha (IFN), lamivudine (LAM), entecavir (ETV), adefovir dipivoxil (ADV).
- Analysis of drugs approved for HIV and active against HBV: LAM, tenofovir disoproxil fumarate (TDF), emtricitabine (FTC).
- Evaluation of drug efficacy, resistance profiles, and suitability for different patient subgroups.
Main Results:
- IFN shows decreased response in co-infected patients.
- LAM and FTC are effective but associated with high HBV resistance rates.
- ETV, ADV, and TDF are effective against wild-type and LAM-resistant HBV; ADV and TDF have favorable resistance profiles.
Conclusions:
- For HBV-naive patients not requiring HIV therapy, interferon, ADV, or ETV are preferable.
- Combination therapy with TDF plus FTC or LAM is recommended for patients needing treatment for both viruses.
- TDF should be included in antiretroviral regimens for patients with lamivudine-resistant HBV.
Abstract:
Recommendations for the treatment of chronic hepatitis B (CHB) in HIV-infected patients is complex due to the lack of controlled trials and the dual activity of therapeutic agents on both viruses. Thus, proposals for optimal anti-HBV therapy in HIV-infected patients should be pragmatic using the knowledge from HBV mono- and HIV/HBV co-infected studies. There are four approved drugs for the treatment of CHB which include interferon alpha (IFN), lamivudine (LAM), entecavir (ETV) and adefovir dipivoxil (ADV). LAM, tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC) are approved for HIV and active against HBV. Studies with IFN are limited in HIV/HBV co-infected patients but suggest a decreased response compared with HBV mono-infected patients. LAM and FTC are effective against HBV but are associated with a high rate of HBV resistance. ETV, ADV and TDF are effective against wild-type and LAM-resistant HBV with a favourable resistance profile shown for ADV and TDF. Interferon, ADV or ETV are the preferable drugs in HBV naive patients who do not require HIV therapy. Combination of TDF plus FTC or LAM should be proposed in patients with therapeutic indication for both viruses. TDF should be included in the anti-retroviral regiment of patients with HBV resistance to lamivudine.
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