Evidence map›Paper›PMID 40473642›Full record

ArticleNPJ vaccines2025

Chimeric hemagglutinin and M2 mRNA vaccine for broad influenza subtype protection.

Dongrong Yi, Qian Liu, Saisai Guo, Quanjie Li, Yongxin Zhang, Ning Li, Qili Zhang, Kai Lv, Ni An, Lu Han and 14 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

24 authors.

Dongrong Yi *Institute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Qian Liu *Institute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Saisai Guo *Institute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Quanjie Li *Institute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Yongxin Zhang *Institute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Ning Li *RinuaGene Biotechnology Co., Ltd., Suzhou, Jiangsu, China.
Qili ZhangRinuaGene Biotechnology Co., Ltd., Suzhou, Jiangsu, China.
Kai LvInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Ni AnBeijing Tsinghua Changgung Hospital, Beijing, China.
Lu HanRinuaGene Biotechnology Co., Ltd., Suzhou, Jiangsu, China.
Hua ChenRinuaGene Biotechnology Co., Ltd., Suzhou, Jiangsu, China.
Yi WangRinuaGene Biotechnology Co., Ltd., Suzhou, Jiangsu, China.
Chunyan ChangRinuaGene Biotechnology Co., Ltd., Suzhou, Jiangsu, China.
Huihan ShaoInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Jing WangInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Xiaoyu LiInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China.
Linlin BaoInstitute of Laboratory Animals Science, Chinese Academy of Medical Sciences, Beijing, China.
Dayan WangNational Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
Guoyang LiaoInstitute of Medical Biology, Chinese Academy of Medical Sciences, Kunming, China.
Chunjian HuangRinuaGene Biotechnology Co., Ltd., Suzhou, Jiangsu, China.
Weiguo ZhangRinuaGene Biotechnology Co., Ltd., Suzhou, Jiangsu, China. weiguo.zhang@rinuagene.com.
Yijie DongRinuaGene Biotechnology Co., Ltd., Suzhou, Jiangsu, China. yijie.dong@rinuagene.com.
Yuelong ShuKey Laboratory of Pathogen Infection Prevention and Control (MOE), State Key Laboratory of Respiratory Health and Multimorbidity, National Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China. yshu@mail.ipbcams.ac.cn.
Shan CenInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing, China. shancen@imb.pumc.edu.cn.ORCID http://orcid.org/0000-0003-3358-0411

Funding

Natural Science Foundation of Beijing Municipality (Beijing Natural Science Foundation) 7242097
6 · The paper itself

Abstract

Since multiple and unpredicted influenza viruses cause seasonal epidemics and even high-risk pandemics, developing a universal influenza vaccine is essential to provide broad protection against various influenza subtypes. Combined with the mRNA lipid nanoparticle-encapsulated (mRNA-LNP) vaccine platform and chimeric immunogen strategy, we developed a novel cocktail mRNA vaccine encoding chimeric HAs (cH5/1-BV, cH7/3) and intact M2 (termed Fluaxe), which confers broad protection against major circulating IAVs and IBVs, as well as highly pathogenic avian influenza. Two-dose intramuscular immunization of Fluaxe in mice elicited cross-reactive neutralizing antibodies, T cell responses, and long-lived immunity, resulting in robust protection against multiple lethal influenza virus infections and severe acute lung injuries. In particular, intramuscular administration stimulated systemic immunity together with a prominent lung tropism of memory cells. Moreover, Fluaxe immunization inhibited the inflammatory response induced by influenza infection. In summary, we conclude that Fluaxe can elicit broad cross-protection against numerous influenza subtypes.

Identifiers

PMID40473642
PMCPMC12141470

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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.