Evidence map›Paper›PMID 30866759›Full record

ArticleEmerging microbes & infections2019

Protection against homo and hetero-subtypic influenza A virus by optimized M2e DNA vaccine.

Yanfeng Yao, Huadong Wang, Jianjun Chen, Zhiyong Shao, Bin He, Jie Chen, Jiaming Lan, Quanjiao Chen, Ze Chen

Open access · goldAbstract read
In one paragraph

Article in Emerging microbes & infections, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
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

14 citing papers in PubMed, 18 citations in OpenAlex.

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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

9 authors at 5 institutions in 2 countries.

Yanfeng Yaoa National Biosafety Laboratory, Wuhan Institute of Virology , Chinese Academy of Sciences , Wuhan , People's Republic of China.
Huadong Wangc Center for Brain Science, Key Laboratory of Magnetic Resonance in Biological Systems and State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics , Chinese Academy of Sciences , Wuhan , People's Republic of China.
Jianjun Chend CAS Key Laboratory of Special Pathogens and Biosafety , Chinese Academy of Sciences , Hubei , People's Republic of China.ORCID http://orcid.org/0000-0002-2966-2388
Zhiyong Shaob Institute of Animal Husbandry and Veterinary Science , Wuhan Academy of Agricultural Science and Technology , Wuhan , People's Republic of China.
Bin Heb Institute of Animal Husbandry and Veterinary Science , Wuhan Academy of Agricultural Science and Technology , Wuhan , People's Republic of China.
Jie Chenb Institute of Animal Husbandry and Veterinary Science , Wuhan Academy of Agricultural Science and Technology , Wuhan , People's Republic of China.
Jiaming Lane Department of Pathogenic Biology , Hebei Medical University , Shijiazhuang , People's Republic of China.
Quanjiao Chend CAS Key Laboratory of Special Pathogens and Biosafety , Chinese Academy of Sciences , Hubei , People's Republic of China.
Ze Chenf College of Life Science , Hunan Normal University , Changsha , People's Republic of China.
Chinese Academy of Sciences · CNAnimal Science Research Institute · CNHebei Medical University · CNHunan Normal University · CNWuhan Institute of Virology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current influenza vaccines provide hemagglutinin strain-specific protection, but rarely provide cross-protection against divergent strains. It is, therefore, particularly important to develop a universal vaccine against conserved proteins or conserved regions of the virus. In this study, we used N-terminal extracellular region of the influenza virus M2 protein (M2e) as the target antigen and constructed two optimized M2e DNA vaccines (p-tPA-p3M2e and p-p3M2e) with increased antigenic epitope density and enhanced antigen secretion. Both vaccines induced high M2e-specific humoral and cellular immune responses in the vaccinated mice. These two vaccines also conferred protection against a lethal infection of homo-subtypic H1N1 virus, with p-tPA-p3M2e being the most effective. In addition, p-tPA-p3M2e also showed cross-protection against different subtypes of the influenza virus (H9N2, H6N6, and H10N8) at varying rates (80%, 40%, and 20%, respectively). After passive immunization, M2e DNA vaccine-induced antibodies in the sera provided complete protection against homologous virus challenge. An analysis of the mechanism underlying this immunization-mediated protection indicates that M2e-specific IgG and T-cell immune responses may play critical roles in the prevention of infection and viral clearance. Taken together, our results indicate that this optimized M2e DNA vaccine is a promising candidate for the development of a universal, broad-spectrum influenza virus vaccine.

Indexed as

AnimalsCross ProtectionDogsHEK293 CellsHumansImmunity, CellularImmunity, HumoralImmunization, PassiveInfluenza A Virus, H1N1 SubtypeInfluenza, HumanInfluenza VaccinesMadin Darby Canine Kidney CellsMiceOrthomyxoviridae InfectionsVaccines, DNAViral Matrix ProteinsInfluenza VaccinesM2 protein, Influenza A virusVaccines, DNAViral Matrix ProteinsViroporin ProteinsInfluenzaM2eoptimized M2e DNA vaccinetPAUniversal influenza vaccine

Identifiers

PMID30866759
PMCPMC6455129
OpenAlexW2909089602

What OpenQuestion holds

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LicenceCC BY
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.