Evidence map›Paper›PMID 41046834›Full record

ArticleVaccine2025

Protective efficacy of the UniFluVec influenza vaccine vector against the highly pathogenic influenza A/Indonesia/5/2005 (H5N1) strain in ferrets.

Julia Romanova, Artem Krokhin, Boris Ferko, Dirk Pleimes, Eva Vareckova, Frantisek Kostolansky, Andrej Egorov

Abstract read
In one paragraph

Article in Vaccine, 2025. 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

7 authors.

Julia RomanovaCapricorn Technologies GmbH, Technopark 1C, A-3430 Tulln, Austria. Electronic address: Julia.Romanova@capricorn-consilium.com.
Artem KrokhinCapricorn Technologies GmbH, Technopark 1C, A-3430 Tulln, Austria. Electronic address: Artem.Krokhin@capricorn-consilium.com.
Boris FerkoEF-Bio GmbH s.r.o., Harmonia 3053, 90001 Modra, Slovak Republic.
Dirk PleimesTreamid Therapeutics GmbH, Robert-Rössle-Straße 10, 13125 Berlin, Germany. Electronic address: dirk.pleimes@scinspire.org.
Eva VareckovaInstitute of Virology, Biomedical Research Centre, Dúbravská cesta 9, 841 04 Bratislava, Slovak Republic. Electronic address: Eva.Vareckova@savba.sk.
Frantisek KostolanskyInstitute of Virology, Biomedical Research Centre, Dúbravská cesta 9, 841 04 Bratislava, Slovak Republic. Electronic address: Frantisek.Kostolansky@savba.sk.
Andrej EgorovCapricorn Technologies GmbH, Technopark 1C, A-3430 Tulln, Austria. Electronic address: andrej.egorov@capricorn-consilium.com.

Funding

NIAID NIH HHS HHSN272201700029I
6 · The paper itself

Abstract

backgroundThe emergence of new influenza strains with unpredictable antigenic properties poses a significant vaccination challenge. The increasing incidence of human H5 infections underscores the urgent need for effective pre-pandemic vaccines.

methodsThe UniFluVec and UniFluVec-wtNS1 viruses were designed as H1N1pdm vaccine candidates. Both viruses contained a heterologous A/Singapore/1/57-like (H2N2) NEP gene, which served as an attenuation factor. UniFluVec additionally carried a truncated to 124 amino acids NS1 gene, and an insertion of conserved influenza sequences. UniFluVec-wtNS1 retained the wild-type NS1 gene. The impact of NS1 and NEP modifications on attenuation and phenotypic markers was assessed in cells and mice. Safety and prophylactic efficacy were assessed in ferrets following a single intranasal immunisation with the maximum feasible dose (8.7 log

resultsModifications in NS1 and NEP independently and synergistically induced a temperature-sensitive phenotype and enhanced type I/II interferon response, resulting in a highly attenuated vaccine profile. UniFluVec, incorporating both modifications within the NS genomic segment, demonstrated superior viral clearance, reducing lung damage, and ensuring 100 % survival in infected animals.

conclusionThe replication-deficient UniFluVec vector demonstrates safety, immunogenicity, and protective efficacy against the heterologous HPAIV strain in ferrets following a single intranasal administration.

Indexed as

Genetic VectorsInfluenza A Virus, H5N1 SubtypeInfluenza VaccinesOrthomyxoviridae InfectionsAdministration, IntranasalAnimalsAntibodies, ViralFemaleFerretsInfluenza A Virus, H1N1 SubtypeMiceMice, Inbred BALB CVaccine EfficacyVaccines, AttenuatedViral Nonstructural ProteinsAntibodies, ViralInfluenza VaccinesINS1 protein, influenza virusVaccines, AttenuatedViral Nonstructural ProteinsAvian influenzaChallenge modelFerretsLive influenza vaccineReplication-deficient virusUniFluVec vector

Identifiers

PMID41046834
PMCPMC13669906

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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.