Evidence map›Paper›PMID 39881325›Full record

ArticleJournal of nanobiotechnology2025

Avian influenza mRNA vaccine encoding hemagglutinin provides complete protection against divergent H5N1 viruses in specific-pathogen-free chickens.

Zhaoyang Wang, Chongyu Tian, Jiahang Zhu, Shiqian Wang, Xiang Ao, Yanjuan He, Huixin Chen, Xiuying Liao, Deming Kong, Yongfei Zhou and 3 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

13 authors.

Zhaoyang Wang *College of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Chongyu Tian *Institute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, 518132, China.
Jiahang Zhu *College of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Shiqian WangCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Xiang AoCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Yanjuan HeCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Huixin ChenCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Xiuying LiaoCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Deming KongCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Yongfei ZhouInstitute of Hemu Biotechnology, Beijing Hemu Biotechnology Co., Ltd, Beijing, 102206, China.
Wanbo TaiInstitute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, 518132, China. taiwb@szbl.ac.cn.
Ming LiaoCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China. mliao1968@163.com.
Huiying FanCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China. fanhy@scau.edu.cn.

Funding

National Key Research and Development Program of China 2022YFD1801003the Innovation Leading Team Program of Guangzhou City 202009020009the National Natural Science Foundation of China 82271872
6 · The paper itself

Abstract

backgroundThe rapid mutation of avian influenza virus (AIV) poses a significant threat to both the poultry industry and public health. Herein, we have successfully developed an mRNA-LNPs candidate vaccine for H5 subtype highly pathogenic avian influenza and evaluated its immunogenicity and protective efficacy.

resultsIn experiments on BALB/c mice, the vaccine candidate elicited strong humoral and a certain cellular immune responses and protected mice from the heterologous AIV challenge. Antibody and splenocyte passive transfer assays in mice suggested that antibodies played a crucial role in providing protection. Experiments involving SPF chickens have revealed that two doses of the 5 µg vaccine candidate in this study provided 100% complete protection against homologous strains, but only 50% complete protection against heterologous strains. Even immunization with two doses of the 15 µg vaccine candidate resulted in 90% complete protection against heterologous strains. To enhance the immune efficacy of the candidate vaccine, we designed 6 sequences with different secondary structures and screened out the candidate sequence with the highest expression (SY2-HA mRNA). Experiments on SPF chickens showed that two doses of 5 µg SY2-HA mRNA-LNP vaccine provided 100% complete protection against homologous and heterologous H5N1 AIV strains. Immunization tests with the SY2-HA mRNA-LNP vaccine were repeated in the SPF chicken model, inducing antibody production levels that are consistent with previous tests and providing 100% complete protection against both homologous and heterologous strains of the virus, indicating that the vaccine has a stable immune efficacy.

conclusionsThe vaccine developed in this study provides complete protection against divergent H5N1 AIV strains in chickens, offering a promising approach for the future development of mRNA vaccines against multivalent avian influenza subtypes.

Indexed as

Hemagglutinin Glycoproteins, Influenza VirusInfluenza A Virus, H5N1 SubtypeInfluenza in BirdsInfluenza VaccinesAnimalsAntibodies, ViralChickensFemaleMiceMice, Inbred BALB CRNA, MessengerSpecific Pathogen-Free OrganismsAntibodies, ViralHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesRNA, MessengerH5N1HALipid nanoparticlemRNA secondary structuremRNA vaccine

Identifiers

PMID39881325
PMCPMC11776166

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.