# The Role of Prior HBV Infection on the Efficacy of 3TC/DTG as a Maintenance Therapy

**Authors:** Tommaso Matucci, Sara Occhineri, Alessandra Palomba, Maria Linda Vatteroni, Laura Del Bono, Marina Polidori, Riccardo Iapoce, Alberto Borghetti, Marco Falcone

PMC · DOI: 10.3390/v18010142 · Viruses · 2026-01-22

## TL;DR

This study found that prior hepatitis B virus exposure may increase the risk of treatment failure when switching to a simplified HIV regimen of 3TC/DTG.

## Contribution

The study identifies prior HBV infection as a potential risk factor for virological failure in PWH on 3TC/DTG.

## Key findings

- 8 out of 188 patients experienced virological failure over 5082 patient-years of follow-up.
- Anti-HBc positivity was associated with a 4.8-fold increased risk of virological failure.
- Those with anti-HBc positivity and prior tenofovir use had a 15-fold higher risk of virological failure.

## Abstract

Lamivudine/dolutegravir (3TC/DTG) is an effective and well-tolerated antiretroviral regimen for most people with HIV (PWH) who are virologically suppressed; however, specific clinical characteristics, such as prior hepatitis B virus (HBV) exposure or archived resistance-associated mutations (RAMs), may influence the risk of virological failure (VF). We conducted a retrospective, monocentric cohort study to evaluate the incidence and predictors of VF among PWH who switched to 3TC/DTG after achieving virological suppression (HIV-RNA < 50 copies/mL). A total of 188 PWH were included. Over 5082 patient-years of follow-up (PYFU), 8 individuals (4.3%) experienced VF, corresponding to an incidence rate of 1.45 per 1000 PYFU. The cumulative probabilities of VF at 1, 2, 3, 4, and 5 years were 0.6%, 2.7%, 2.7%, 4.2%, and 22.3%, respectively. In exploratory multivariable analyses, anti-HBc positivity was associated with an increased risk of VF (adjusted hazard ratio [aHR] 4.80, 95% CI 1.03–22.43; p = 0.046). After adjustment for age and sex, individuals with anti-HBc positivity who had switched from a tenofovir-containing regimen showed the highest risk of VF compared with anti-HBc-negative individuals without prior tenofovir exposure (aHR 15.06, 95% CI 1.40–161.38; p = 0.025). Given the limited number of virological events, these findings should be interpreted with caution. Nevertheless, they suggest that prior HBV exposure, particularly in the context of tenofovir discontinuation, may represent a clinically relevant factor when considering simplification to 3TC/DTG.

## Linked entities

- **Chemicals:** lamivudine (PubChem CID 60825), dolutegravir (PubChem CID 54726191), tenofovir (PubChem CID 464205)

## Full-text entities

- **Genes:** KRT88P (keratin 88, pseudogene) [NCBI Gene 85348] {aka HBC, KRT122P, KRTHBP3}
- **Diseases:** HBV Infection (MESH:D006509)
- **Chemicals:** DTG (MESH:C562325), tenofovir (MESH:D000068698), 3TC (MESH:D019259)
- **Species:** Hepatitis B virus (no rank) [taxon 10407], Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12846516/full.md

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Source: https://tomesphere.com/paper/PMC12846516