Evidence map›Paper›PMID 40348847›Full record

ArticleScientific reports2025

Comparison of the induction of neutralizing antibodies against Bas congo virus using several vaccine modalities.

Eun-Sil Park, Tomoki Yoshikawa, Hideki Tani, Masanobu Kimura, Yoshihiro Kaku, Koichi Imaoka, Ken Maeda, Masayuki Saijo, Shigeru Morikawa

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 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
–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

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

9 authors.

Eun-Sil ParkDepartment of Veterinary Science, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, 162-8640, Japan. peunsil@niid.go.jp.
Tomoki YoshikawaDepartment of Virology I, National Institute of Infectious Diseases, Japan Institute for Health Security, Musashimurayama, 208-0011, Japan.
Hideki TaniDepartment of Virology, Toyama Institute of Health, Toyama, 939-0363, Japan.
Masanobu KimuraResearch Center for Biosafety, Laboratory Animal and Pathogen Bank, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, 162-8640, Japan.
Yoshihiro KakuDepartment of Veterinary Science, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, 162-8640, Japan.
Koichi ImaokaResearch Center for Biosafety, Laboratory Animal and Pathogen Bank, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, 162-8640, Japan.
Ken MaedaDepartment of Veterinary Science, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, 162-8640, Japan.
Masayuki SaijoDepartment of Virology I, National Institute of Infectious Diseases, Japan Institute for Health Security, Musashimurayama, 208-0011, Japan.
Shigeru MorikawaDepartment of Veterinary Science, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, 162-8640, Japan.

Funding

Japan Agency for Medical Research and Development 19fk0108072Japan Agency for Medical Research and Development 24fk0108660Japan Agency for Medical Research and Development,Japan 22fk0108615Japan Society for the Promotion of Science JP22K08612Japan Society for the Promotion of Science,Japan 17K18386
6 · The paper itself

Abstract

The Bas-Congo virus (BASV) is a novel rhabdovirus that causes viral hemorrhagic fever in 2009. Since BASV has not been isolated, there is limited information on BASV, and potential therapeutics or vaccines have not yet been developed. In the present study, we used the synthetic cDNA of the BASV-G protein to develop 4 different types of vaccine, using a recombinant BASV-G protein, a plasmid DNA that expresses the BASV-G protein, a recombinant vaccinia virus that expresses the BASV-G protein, and a pseudotype virus based on hydrogen peroxide-inactivated vesicular stomatitis virus (VSV) that expresses the BASV-G protein (BASVpv). BASVpv was generated and used for the evaluation of neutralizing antibodies and the induction of virus neutralizing antibody upon inoculation (BASVpv/GFP) of these candidates in rabbits. The results showed that both the recombinant vaccinia virus and the hydrogen peroxide-inactivated VLPs effectively induced neutralizing antibodies, even with a single inoculation.

Indexed as

Antibodies, NeutralizingAntibodies, ViralViral VaccinesAnimalsRabbitsVaccinia virusViral Envelope ProteinsAntibodies, NeutralizingAntibodies, ViralViral Envelope ProteinsViral Vaccines

Identifiers

PMID40348847
PMCPMC12065830

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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.