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Therapeutic management and evolution of chronic hepatitis B: does HIV still have an impact? The EPIB 2012 study
Lionel Piroth1, Stanislas Pol2, Patrick Miailhes3
1Infectious Diseases Department, CHU and UMR 1347, University of Burgundy, Dijon, France.
Insights
Management of chronic hepatitis B (CHB) in HIV-positive patients has improved, with better HBV DNA undetectability and reduced hepatocellular carcinoma risk. This is likely due to HAART and increased HBV therapy use, mitigating HIV
Area of Science:
- Hepatology
- Virology
- Infectious Diseases
Background:
- Chronic hepatitis B (CHB) management and outcomes in HIV-positive versus HIV-negative patients are compared.
- HIV-positive patients often present with more comorbidities and advanced disease markers.
Purpose of the Study:
- To compare the management and evolution of CHB in HIV-positive and HIV-negative patients.
- To assess the impact of HIV on CHB progression and treatment outcomes.
Main Methods:
- Retrospective analysis of 709 patients with HBs antigenemia from 19 French centers.
- Data collected via standardized questionnaires from the first visit onwards.
Main Results:
- HIV-positive patients had less CHB assessment but received more HBV therapy (95.3% vs 56.8%) and achieved higher HBV undetectability (80.8% vs 55.1%).
- Hepatocellular carcinoma was less frequent in HIV-positive patients (0.7% vs 4.7%).
- Undetectable HBV was associated with longer HBV therapy and older age, not HIV status.
Conclusions:
- Despite assessment gaps, HIV's negative impact on CHB evolution is diminishing.
- Highly active antiretroviral therapy (HAART) and increased HBV treatment likely improve CHB outcomes in coinfected patients.
Background & Aims:
To compare the management of chronic hepatitis B (CHB) and its evolution over time in currently followed HIV-positive and HIV-negative patients.
Methods:
A total of 709 consecutive patients with past or present positive HBs antigenemia seen in October 2012 in 19 French participating centres were included. The data were retrospectively collected from the first visit onwards through standardized questionnaires.
Results:
Chronic hepatitis B was less often assessed in the 299 HIV-positive patients, who were older, more likely to be male, excessive alcohol drinkers and HBe antigen-, HCV- and HDV-positive. They were also followed up for a longer time (11.3 +/-8.8 vs. 8.6 +/-6.9 years, P < 10(-3) ) and were more frequently treated for HBV (95.3% vs. 56.8%, P < 10(-3) ). HBV was undetectable at the last visit in 80.8% of HIV-positive vs. 55.1% of HIV-negative patients (P < 10(-3) ). In multivariate analyses, undetectable HBV was significantly associated with older age, lower baseline HBV DNA, longer HBV therapy and no previous lamivudine monotherapy, but not with HIV. Cirrhosis was associated with age, male gender, Asian origin, alcoholism, HCV, HDV, but not with HIV infection. Hepatocellular carcinoma, less frequently observed in HIV-positive patients (0.7% vs. 4.7%, P = 0.002), was positively associated with age, male gender, cirrhosis and negatively associated with HIV infection (OR 0.15, 95%CI 0.03-0.67, P = 0.01).
Conclusions:
Although the assessment of CHB still has to be improved in HIV-positive patients, the negative impact of HIV on the virological, histological and clinical evolution of CHB seems to be disappearing, probably because of the immunovirological impact of HAART and the more frequent and longer use of HBV therapy.
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