Evidence map›Paper›PMID 41746994›Full record

ArticlePloS one2026

Hepatitis B immunity and vaccine completion among adults at increased risk for hepatitis B infection in Zambia.

Enock Syabbalo, Sydney Mpisa, Michael J Vinikoor, Mercy Wamundila, Likando Munalula, Taonga Musonda, Ruth Phiri, Paul Kelly, Chloe Thio, David L Thomas and 1 more

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Enock SyabbaloUniversity Teaching Hospital, Lusaka, Zambia.ORCID https://orcid.org/0009-0001-8372-1131
Sydney MpisaUniversity Teaching Hospital, Lusaka, Zambia.
Michael J VinikoorUniversity of Zambia, Lusaka, Zambia.
Mercy WamundilaTropical Gastroenterology and Nutrition Group, Lusaka, Zambia.
Likando MunalulaTropical Gastroenterology and Nutrition Group, Lusaka, Zambia.
Taonga MusondaTropical Gastroenterology and Nutrition Group, Lusaka, Zambia.
Ruth PhiriTropical Gastroenterology and Nutrition Group, Lusaka, Zambia.
Paul KellyUniversity of Zambia, Lusaka, Zambia.
Chloe ThioJohns Hopkins University, Baltimore, Maryland, United States of America.
David L ThomasJohns Hopkins University, Baltimore, Maryland, United States of America.
Edford SinkalaUniversity Teaching Hospital, Lusaka, Zambia.

Funding

Mechanisms of HBV Functional Cure During Tenofovir-based ART in HIV/HBV CoinfectionR01AI147727 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Michael Jeffrey Vinikoor · 2019 to 2026
$3.9M
HBV-specific T cell immunity in HBV/HIV coinfectionR37AI179640 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GEORG Michael LAUER, Michael Jeffrey Vinikoor · 2023 to 2026
$2.9M
Spatial omics to understanding HBV control in people with HIV coinfectionR01AI195435 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI Robert E Schwartz, Michael Jeffrey Vinikoor · 2025 to 2026
$1.5M
NIAID NIH HHS R01 AI147727NIAID NIH HHS R01 AI195435NIAID NIH HHS R37 AI179640
6 · The paper itself

Abstract

backgroundBecause of its low cost and lasting effects, hepatitis B virus (HBV) vaccination of adults in Africa could significantly contribute to viral elimination. Among at-risk adult populations there are few data to inform vaccine implementation, including on pre-existing immunity and vaccine uptake. We serologically profiled adults with specific risk factors for HBV infection in urban Zambia and evaluated their uptake of vaccine.

methodsAt a tertiary hospital in Lusaka, we recruited hepatitis B surface antigen-negative adult (age 18+) contacts to people with chronic HBV, health workers (HCWs), and people with HIV (PLWH). After we jointly collected blood and gave the first HBV vaccine dose (blind to the full serological profile), we called back those whose results showed insufficient surface antibodies (anti-HBs) to complete the 3-dose series at 1 and 6 months, and we reimbursed transport costs. Stratified by group, we described the proportions of participants with past vaccination, resolved infection (anti-HBc-positive regardless of anti-Hbs status), isolated core antibodies (anti-HBc-positive and anti-HBs-negative), and neither antibody. We described the correlates of resolved infection. We described completion of the vaccine series in anti-HBs-negatives. In those with isolated core antibodies, we explored the incidence of an anamnestic response based on post-first-dose anti-HBs > 10 IU/ml and>= 1-log increase from baseline.

results616 adults (median age, 32.2 years, IQR [26.7-43.8]; 61.2% women) enrolled, including 333 contacts, 213 HCWs, and 70 PLWH. Half had neither antibody, including 68.5% of health workers. Prior vaccination was seen in 8.3% overall, including 11.3% of HCWs. Resolved infection was present for 39.3% and was more prevalent with increased age and among contacts. Isolated core was present in 59 (9.6% overall and 24.7% of those with resolved infection) participants. Among the 383 participants eligible for vaccination, 377 (98.4%) received 1 dose, 190 (49.6%) received 2 doses, and 54 (14.1%) completed the series. Among 18 individuals with isolated core antibodies, none had detectable HBV DNA, and 9 (50%) had an anamnestic response. DISCUSSION: Most adults at risk for HBV in Lusaka, Zambia, had inadequate immunity, which could undermine HBV elimination. High resolved infection rate in contacts supports the role of index testing in HBV case finding. Low vaccine completion, despite vaccine access and addressing transportation costs, was striking and underscores the need for integrated behavioral science approaches to improve implementation of this potentially cost-effective intervention. Low rates of anamnestic response in people with anti-HBc-positivity should be further studied in Africa.

Indexed as

Hepatitis BHepatitis B VaccinesHepatitis B virusAdolescentAdultFemaleHepatitis B AntibodiesHIV InfectionsHumansMaleMiddle AgedRisk FactorsVaccinationYoung AdultZambiaHepatitis B AntibodiesHepatitis B Vaccines

Identifiers

PMID41746994
PMCPMC12944761

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.