Evidence map›Paper›PMID 40303775›Full record

ArticleTransboundary and emerging diseases2023

A Bivalent Bacterium-like Particles-Based Vaccine Induced Potent Immune Responses against the Sudan Virus and Ebola Virus in Mice.

Shengnan Xu, Wujian Li, Cuicui Jiao, Zengguo Cao, Fangfang Wu, Feihu Yan, Hualei Wang, Na Feng, Yongkun Zhao, Songtao Yang and 2 more

Abstract read
In one paragraph

Article in Transboundary and emerging diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

12 authors.

Shengnan XuCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, China.
Wujian LiChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.ORCID https://orcid.org/0000-0002-3993-8499
Cuicui JiaoCollege of Veterinary Medicine, Jilin University, Changchun, China.
Zengguo CaoChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Fangfang WuChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Feihu YanChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Hualei WangCollege of Veterinary Medicine, Jilin University, Changchun, China.
Na FengChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Yongkun ZhaoChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Songtao YangChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Jianzhong WangCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, China.ORCID https://orcid.org/0000-0002-6975-130X
Xianzhu XiaCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, China.ORCID https://orcid.org/0000-0001-5090-1358

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ebola virus disease (EVD) is an acute viral hemorrhagic fever disease causing thousands of deaths. The large Ebola outbreak in 2014-2016 posed significant threats to global public health, requiring the development of multiple medical measures for disease control. Sudan virus (SUDV) and Zaire virus (EBOV) are responsible for severe disease and occasional deadly outbreaks in West Africa and Middle Africa. This study shows that bivalent bacterium-like particles (BLPs)-based vaccine, SUDV-EBOV BLPs (S/ZBLP + 2 + P), generated by mixing SUDV-BLPs and EBOV-BLPs at a 1 : 1 ratio, is immunogenic in mice. The SUDV-EBOV BLPs induced potent immune responses against SUDV and EBOV and elicited both T-helper 1 (Th1) and T-helper 2 (Th2) immune responses. The results indicated that SUDV-EBOV BLPs-based vaccine has the potential to be a promising candidate against SUDV and EBOV infections and provide a strategy to develop universal vaccines for EVD.

Indexed as

Ebola VaccinesEbolavirusHemorrhagic Fever, EbolaVaccines, Virus-Like ParticleAnimalsAntibodies, ViralFemaleMiceMice, Inbred BALB CAntibodies, ViralEbola VaccinesVaccines, Virus-Like Particle

Identifiers

PMID40303775
PMCPMC12017122

What OpenQuestion holds

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Registered trials

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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.