Evidence map›Paper›PMID 35216022›Full record

ArticleViruses2022

Multiple Neuraminidase Containing Influenza Virus-like Particle Vaccines Protect Mice from Avian and Human Influenza Virus Infection.

Hae-Ji Kang, Ki-Back Chu, Keon-Woong Yoon, Gi-Deok Eom, Jie Mao, Min-Ju Kim, Su-Hwa Lee, Eun-Kyung Moon, Fu-Shi Quan

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In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 13 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 2 institutions in 1 country.

Hae-Ji KangDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, Korea.
Ki-Back ChuDepartment of Medical Zoology, Kyung Hee University School of Medicine, Seoul 02447, Korea.
Keon-Woong YoonDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, Korea.
Gi-Deok EomDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, Korea.
Jie MaoDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, Korea.
Min-Ju KimDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, Korea.
Su-Hwa LeeDepartment of Medical Zoology, Kyung Hee University School of Medicine, Seoul 02447, Korea.
Eun-Kyung MoonDepartment of Medical Zoology, Kyung Hee University School of Medicine, Seoul 02447, Korea.ORCID 0000-0003-1121-2052
Fu-Shi QuanDepartment of Medical Zoology, Kyung Hee University School of Medicine, Seoul 02447, Korea.ORCID 0000-0003-0419-9339
Kyung Hee University · KRKyung Hee University Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Avian influenza virus remains a threat for humans, and vaccines preventing both avian and human influenza virus infections are needed. Since virus-like particles (VLPs) expressing single neuraminidase (NA) subtype elicited limited heterosubtypic protection, VLPs expressing multiple NA subtypes would enhance the extent of heterosubtypic immunity. Here, we generated avian influenza VLP vaccines displaying H5 hemagglutinin (HA) antigen with or without avian NA subtypes (N1, N6, N8) in different combinations. BALB/c mice were intramuscularly immunized with the VLPs to evaluate the resulting homologous and heterosubtypic immunity upon challenge infections with the avian and human influenza viruses (A/H5N1, A/H3N2, A/H1N1). VLPs expressing H5 alone conferred homologous protection but not heterosubtypic protection, whereas VLPs co-expressing H5 and NA subtypes elicited both homologous and heterosubtypic protection against human influenza viruses in mice. We observed that VLP induced neuraminidase inhibitory activities (NAI), virus-neutralizing activity, and virus-specific antibody (IgG, IgA) responses were strongly correlated with the number of different NA subtype expressions on the VLPs. VLPs expressing all 3 NA subtypes resulted in the highest protection, indicated by the lowest lung titer, negligible body weight changes, and survival in immunized mice. These results suggest that expressing multiple neuraminidases in avian HA VLPs is a promising approach for developing a universal influenza A vaccine against avian and human influenza virus infections.

Indexed as

AnimalsAntibodies, ViralFemaleHemagglutinin Glycoproteins, Influenza VirusInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeInfluenza A Virus, H5N1 SubtypeInfluenza VaccinesMiceMice, Inbred BALB CNeuraminidaseOrthomyxoviridae InfectionsSurvival AnalysisVaccinationVaccines, Virus-Like ParticleAntibodies, Viralhemagglutinin, avian influenza A virusHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesNeuraminidaseVaccines, Virus-Like Particleavian influenza virusheterosubtypic immunityneuraminidasevirus-like particles

Identifiers

PMID35216022
PMCPMC8875606
OpenAlexW4212774086

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LicenceCC BY
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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.