Evidence map›Paper›PMID 42176113›Full record

ArticleInfectious diseases and therapy2026

HBV Serological Profiles and Vaccination Status in People with HIV in the Transition to a Tenofovir-Sparing Era: Insights from a Large HIV Cohort.

Alberto Foncillas, Lorena De La Mora, Leire Berrocal, Elisa de Lazzari, Júlia Calvo, Abiu Sempere, Ivan Chivite, Alexy Inciarte, Maria Martínez-Rebollar, Berta Torres and 7 more

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Article in Infectious diseases and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Alberto Foncillas *HIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain. foncillas@clinic.cat.
Lorena De La Mora *HIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Leire BerrocalHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Elisa de LazzariHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Júlia CalvoHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Abiu SempereHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Ivan ChiviteHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Alexy InciarteHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Maria Martínez-RebollarHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Berta TorresHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Ana González-CordónHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Jose Luís BlancoHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
José M MiróHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Esteban MartínezHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Montserrat LagunoHIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Josep Mallolas *HIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain.
Juan Ambrosioni *HIV Unit, Infectious Diseases Service. Hospital Clínic of Barcelona - Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Villarroel Street 170, 08036, Barcelona, Spain. ambrosioni@clinic.cat.ORCID http://orcid.org/0000-0003-0048-5506

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe increasing adoption of tenofovir (TXF)-sparing antiretroviral therapy (ART) raises concerns regarding hepatitis B virus (HBV) susceptibility and reactivation risk among people with HIV (PWH). We characterized HBV serological profiles and vaccination status according to ART composition in a real-world cohort.

methodsA cross-sectional study of all PWH in active follow-up at Hospital Clínic, Barcelona, as of 30 June 2025. ART regimens were categorized as TXF-containing or TXF-sparing, with or without lamivudine (3TC). HBV serological patterns were classified as chronic infection, serologically resolved infection, isolated HBV core antibody (anti-HBc), no exposure/immunity, and vaccine-induced immunity. Demographic and clinical characteristics were compared using nonparametric and chi-squared/Fisher's tests.

resultsAmong the 6437 participants included (82% cisgender men; median age 48 years [IQR 39-58]), 3519 (55%) received TXF-containing and 2918 (45%) TXF-sparing regimens, of whom 1702/2918 (58%) were with 3TC. HBV serological distribution was: 2% chronic infection, 26% serologically resolved infection, 5% isolated anti-HBc, 52% vaccine-induced immunity, and 15% without exposure/immunity (50% documented prior vaccination attempts, 32% nonresponders, and 31% with prior anti-HBs detection). Overall, 1280 (20%) lacked protective HBV immunity (isolated anti-HBc or negative serology for all markers), including 530 (41%) on TXF-free regimens. TXF recipients were younger (47 versus 50 years, p < 0.001), more often migrants (58% versus 49%, p < 0.001), had lower suppression rates (91% versus 97%, p < 0.001), a higher proportion of previous virological failure(s) (26% versus 21%, p < 0.001), and a lower number of prior ART regimens (median 3 versus 4, p < 0.001).

conclusionsOne in five PWH lacked effective HBV immunity, including 41% of whom were receiving TXF-sparing strategies. In the context of increasing use of TXF-sparing strategies, improvements in systematic HBV screening, vaccination, and risk-based monitoring are essential to prevent HBV-related morbidity.

Indexed as

HBV immunityHBV reactivationHepatitis B virusHIVTenofovir-sparing therapy

Identifiers

PMID42176113
PMCPMC13280293

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