Circulating HBV RNA and hepatitis B core-related antigen as determinants of HBsAg loss in persons with HIV in Europe

Lorin Begré, Anders Boyd, Marie-Laure Plissonnier, Barbara Testoni, Charles Béguelin, Franziska Suter-Riniker, Caroline Scholtès, Jürgen K Rockstroh, Karine Lacombe, Lars Peters, Marintha Heil, Massimo Levrero, Andri Rauch, Fabien Zoulim, Gilles Wandeler, Swiss HIV Cohort Study, EuroSIDA and French HIV/HBV and Biliver cohorts, EuroSIDA Study Group, French HIV/HBV and Biliver cohorts

Abstract

BACKGROUND & AIMS: HBsAg loss improves clinical outcomes in persons with HIV and HBV coinfection. We aimed to evaluate if hepatitis B core-related antigen and circulating HBV RNA levels were associated with HBsAg loss in Euro-B, a multi-cohort collaboration including data from the Swiss HIV Cohort Study, EuroSIDA, and the French HIV/HBV cohort.

METHODS: We included persons with HIV, a positive HBsAg, and ≥6 months of follow-up on tenofovir-containing antiretroviral therapy. We evaluated quantitative HBsAg, HBV DNA, hepatitis B core-related antigen, and HBV RNA levels over time and assessed HBsAg loss (i.e. quantitative HBsAg <0.05 IU/ml) during tenofovir therapy.

RESULTS: Among 599 participants median age was 41 years (IQR 35-47), 18.4% were female and 47.3% HBeAg-positive. We observed HBsAg loss in 12.9% of participants after 2 years and in 18.2% during a median follow-up of 8.2 years (IQR 3.6-13.1). Individuals who were HBeAg-negative were more likely to have a negative hepatitis B core-related antigen and HBV RNA below the detection limit than participants who were HBeAg-positive. Quantitative HBsAg ≤1,000 IU/ml at baseline was the strongest predictor of HBsAg loss regardless of HBeAg status. Additionally, HBsAg loss was associated with lower baseline HBV RNA levels (odds ratio 0.66, 95% CI 0.49-0.88) and higher baseline HBV DNA levels in participants who were HBeAg-positive.

CONCLUSIONS: In this European cohort of persons with HIV/HBV, 18% experienced HBsAg loss during tenofovir-containing antiretroviral therapy. In addition to low baseline quantitative HBsAg levels, HBV RNA may predict HBsAg loss in individuals who are HBeAg-positive.

IMPACT AND IMPLICATIONS: The present study builds on a multi-cohort collaboration including persons with HIV/HBV from Europe. It provides estimates on the probability of HBsAg loss during long-term tenofovir-containing antiretroviral therapy and describes the potential of the novel biomarkers HBV RNA and hepatitis B core-related antigen as its predictors. The discrepancies regarding HBV RNA and HBcrAg levels before and during therapy observed between persons who were HBeAg-negative and HBeAg-positive with HIV/HBV may influence treatment decisions and the development of new treatment strategies.

CLINICAL TRIALS REGISTRATION: The study is registered at ClinicalTrials.gov (NCT04984772).

OriginalsprogEngelsk
Artikelnummer101671
TidsskriftJHEP reports : innovation in hepatology
Vol/bind8
Udgave nummer2
Sider (fra-til)101671
ISSN2589-5559
DOI
StatusUdgivet - feb. 2026

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