Evidence map›Paper›PMID 34451966›Full record

ArticleVaccines2021

Immunogenicity and Antiviral Response of Therapeutic Hepatitis B Vaccination in a Mouse Model of HBeAg-Negative, Persistent HBV Infection.

Anna D Kosinska, Julia Festag, Martin Mück-Häusl, Marvin M Festag, Theresa Asen, Ulrike Protzer

Abstract read
In one paragraph

Article in Vaccines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

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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

6 authors.

Anna D KosinskaInstitute of Virology, Technical University of Munich/Helmholtz Zentrum München, D-81675 Munich, Germany.
Julia FestagInstitute of Virology, Technical University of Munich/Helmholtz Zentrum München, D-81675 Munich, Germany.ORCID 0000-0001-6159-8286
Martin Mück-HäuslInstitute of Virology, Technical University of Munich/Helmholtz Zentrum München, D-81675 Munich, Germany.
Marvin M FestagInstitute of Virology, Technical University of Munich/Helmholtz Zentrum München, D-81675 Munich, Germany.ORCID 0000-0003-1294-8336
Theresa AsenInstitute of Virology, Technical University of Munich/Helmholtz Zentrum München, D-81675 Munich, Germany.
Ulrike ProtzerInstitute of Virology, Technical University of Munich/Helmholtz Zentrum München, D-81675 Munich, Germany.ORCID 0000-0002-9421-1911

Funding

Deutsche Forschungsgemeinschaft TRR179, TP18Helmholtz Association PoC InitiativeHorizon 2020 Framework Programme TherVacB Consortium
6 · The paper itself

Abstract

During the natural course of chronic hepatitis B virus (HBV) infection, the hepatitis B e antigen (HBeAg) is typically lost, while the direct transmission of HBeAg-negative HBV may result in fulminant hepatitis B. While the induction of HBV-specific immune responses by therapeutic vaccination is a promising, novel treatment option for chronic hepatitis B, it remains unclear whether a loss of HBeAg may influence its efficacy or tolerability. We therefore generated an adeno-associated virus (AAV)-vector that carries a 1.3-fold overlength HBV genome with a typical stop-codon mutation in the pre-core region and initiates the replication of HBeAg(-) HBV in mouse livers. Infection of C57BL/6 mice established persistent HBeAg(-) HBV-replication without any detectable anti-HBV immunity or liver damage. HBV-carrier mice were immunized with

Indexed as

chronic hepatitis Bhepatitis B virushepatitis B virus e antigenpre-core mutationprime/boost vaccinationtherapeutic vaccination

Identifiers

PMID34451966
PMCPMC8402308

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.