Evidence map›Paper›PMID 34908443›Full record

ArticleJournal of virology2022

A Single Vaccine Protects against SARS-CoV-2 and Influenza Virus in Mice.

Kangli Cao, Xiang Wang, Haoran Peng, Longfei Ding, Xiangwei Wang, Yangyang Hu, Lanlan Dong, Tianhan Yang, Xiujing Hong, Man Xing and 8 more

Abstract read
In one paragraph

Article in Journal of virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

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  15. A potential bivalent mRNA vaccine candidate protects against both RSV and SARS-CoV-2 infections.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
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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

18 authors.

Kangli Cao *Zhongshan Hospital & Institutes of Biomedical Sciences, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Xiang Wang *Shanghai Public Health Clinical Centergrid.470110.3, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Haoran Peng *Department of Microbiology, Second Military Medical Universitygrid.73113.37, Shanghai, People's Republic of China.
Longfei Ding *Shanghai Public Health Clinical Centergrid.470110.3, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Xiangwei WangShanghai Public Health Clinical Centergrid.470110.3, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Yangyang HuShanghai Public Health Clinical Centergrid.470110.3, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Lanlan DongZhongshan Hospital & Institutes of Biomedical Sciences, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Tianhan YangShanghai Public Health Clinical Centergrid.470110.3, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Xiujing HongZhongshan Hospital & Institutes of Biomedical Sciences, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Man XingDepartment of Pathogen Biology, School of Basic Medical Sciences, Tianjin Medical Universitygrid.265021.2, Tianjin, People's Republic of China.
Duoduo LiShanghai Public Health Clinical Centergrid.470110.3, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Cuisong ZhuShanghai Public Health Clinical Centergrid.470110.3, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Xiangchuan HeZhongshan Hospital & Institutes of Biomedical Sciences, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Chen ZhaoShanghai Public Health Clinical Centergrid.470110.3, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Ping ZhaoDepartment of Microbiology, Second Military Medical Universitygrid.73113.37, Shanghai, People's Republic of China.
Dongming ZhouShanghai Public Health Clinical Centergrid.470110.3, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Xiaoyan ZhangZhongshan Hospital & Institutes of Biomedical Sciences, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.
Jianqing XuZhongshan Hospital & Institutes of Biomedical Sciences, Fudan Universitygrid.8547.e, Shanghai, People's Republic of China.ORCID 0000-0003-0896-9273

Funding

National Natural Science Foundation of China (NSFC) 81761128007
6 · The paper itself

Abstract

The ongoing SARS-CoV-2 pandemic poses a severe global threat to public health, as do influenza viruses and other coronaviruses. Here, we present chimpanzee adenovirus 68 (AdC68)-based vaccines designed to universally target coronaviruses and influenza. Our design is centered on an immunogen generated by fusing the SARS-CoV-2 receptor-binding domain (RBD) to the conserved stalk of H7N9 hemagglutinin (HA). Remarkably, the constructed vaccine effectively induced both SARS-CoV-2-targeting antibodies and anti-influenza antibodies in mice, consequently affording protection from lethal SARS-CoV-2 and H7N9 challenges as well as effective H3N2 control. We propose our AdC68-vectored coronavirus-influenza vaccine as a universal approach toward curbing respiratory virus-causing pandemics.

Indexed as

ChAdOx1 nCoV-19Influenza VaccinesAnimalsCOVID-19FemaleHEK293 CellsHumansInfluenza A Virus, H7N9 SubtypeMiceMice, Inbred BALB CMice, Inbred ICRMice, TransgenicOrthomyxoviridae InfectionsPandemicsSARS-CoV-2ChAdOx1 nCoV-19Influenza Vaccinesadenoviral vectorCOVID-19influenzaSARS-CoV-2 variantsvaccine

Identifiers

PMID34908443
PMCPMC8865568

What OpenQuestion holds

Textmetadata
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.