Evidence map›Paper›PMID 41872755›Full record

ArticleBMC infectious diseases2026

COVID-19 vaccine immunogenicity in Mongolian adults with and without chronic hepatitis.

Viviane Callier, Ganbolor Jargalsaikhan, Munguntsetseg Batkhuu, Renee Ridzon, Sally Hunsberger, Irini Sereti, Kathryn Shaw-Saliba, Shera Weyers, Alyson Francis, Naranjaral Dashdorj

Abstract read
In one paragraph

Article in BMC infectious diseases, 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
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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

10 authors.

Viviane CallierClinical Monitoring Research Program Directorate, Frederick National Laboratory, Frederick, MD, USA. callierv@nih.gov.
Ganbolor JargalsaikhanOnom Foundation, Ulaanbaatar, Mongolia.
Munguntsetseg BatkhuuOnom Foundation, Ulaanbaatar, Mongolia.
Renee RidzonHenry M. Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, MD, USA.
Sally HunsbergerNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA. sally.hunsberger@nih.gov.
Irini SeretiNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Kathryn Shaw-SalibaNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Shera WeyersClinical Monitoring Research Program Directorate, Frederick National Laboratory, Frederick, MD, USA.
Alyson FrancisSystex, Inc., Rockville, MD, USA.
Naranjaral DashdorjOnom Foundation, Ulaanbaatar, Mongolia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMongolia has a high prevalence of liver disease from chronic viral hepatitis infections, which can compromise the immune response. It is unclear whether people with chronic liver disease produce a robust antibody response to the COVID-19 vaccines. We investigated whether the antibody response to the COVID-19 booster vaccination differed between those with and without chronic viral hepatitis from multiple viral types.

methodsParticipants from Mongolia were recruited to the International Study on COVID-19 Vaccine to Assess Immunogenicity, Reactogenicity and Efficacy (InVITE). Demographic information was recorded and participants’ SARS-CoV2 anti-Spike antibody levels were measured at visit 1 (prior to administration of booster vaccine at baseline) and visit 2 (approximately 2 +/-1 months after booster vaccination). We used linear regression to determine if the anti-Spike antibody responses differed between participants with and without different types of chronic viral hepatitis infections.

resultsOverall, there was no significant difference in the anti-Spike antibody response between participants with and without chronic viral hepatitis, a result suggesting that COVID-19 vaccine booster immunogenicity is not affected by chronic hepatitis. Participants with chronic HCV infection produced a robust antibody response, but based on our linear regression analysis, this response seemed to wane faster than in participants without chronic viral hepatitis.

conclusionsOur finding that there was no significant difference in the anti-Spike antibody response between participants with and without chronic viral hepatitis adds to the evidence that the COVID-19 vaccines are immunogenic in people with chronic viral hepatitis, including in those with HBV/HDV coinfection.

Indexed as

COVID-19COVID-19 VaccinesHepatitis C, ChronicImmunogenicity, VaccineAdultAntibodies, ViralFemaleHumansImmunization, SecondaryMaleMiddle AgedMongoliaSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, CoronavirusCOVID-19hepatitisImmunogenicityMongoliaVaccine

Identifiers

PMID41872755
PMCPMC13134319

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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.