ArticleiScience2026
HBV biomarkers outperform host genetic variants in distinguishing occult HBV infection from chronic carriers.
Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- The immunoecology of occult hepatitis B virus infection: genetic remodeling and the immune-mediated microcosm.Frontiers in immunology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This study aimed to determine if host genetic variants could improve the differentiation of occult hepatitis B virus infection (OBI) from overt chronic infection in Chinese blood donors, beyond standard biomarkers. Through a multicenter screening of over 1.14 million donations and a two-year follow-up, we established a cohort of 147 confirmed carriers (74 OBI and 73 overt) who underwent whole-exome sequencing. A model based on 5 routinely available biomarkers-older age, higher HBV DNA Ct value (indicating lower viral load), elevated anti-HBs, decreased anti-HBc, and anti-HBe negativity-achieved high accuracy (AUCs: 0.898-0.910). In contrast, while 9 missense variants showed initial associations, none were validated, and their inclusion reduced model generalizability. We conclude that serological and virological biomarkers are highly effective for OBI risk stratification, whereas common host genetic variants offer minimal incremental value, highlighting the practical superiority of biomarker profiling and setting a benchmark for future research.
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