Evidence map›Paper›PMID 37679361›Full record

ArticleNPJ vaccines2023

A mosaic influenza virus-like particles vaccine provides broad humoral and cellular immune responses against influenza A viruses.

Xuejie Liu, Tianyi Zhao, Liangliang Wang, Zhuolin Yang, Chuming Luo, Minchao Li, Huanle Luo, Caijun Sun, Huacheng Yan, Yuelong Shu

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Stabilized mosaic hemagglutinin immunogens as novel universal influenza virus vaccines.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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  16. Structural characterization of influenza group 1 chimeric hemagglutinins as broad vaccine immunogens.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

10 authors at 2 institutions in 1 country.

Xuejie LiuSchool of Public Health (Shenzhen), Sun Yat-sen University, 518107, Shenzhen, China.
Tianyi ZhaoSchool of Public Health (Shenzhen), Sun Yat-sen University, 518107, Shenzhen, China.
Liangliang WangSchool of Public Health (Shenzhen), Sun Yat-sen University, 518107, Shenzhen, China.
Zhuolin YangSchool of Public Health (Shenzhen), Sun Yat-sen University, 518107, Shenzhen, China.
Chuming LuoSchool of Public Health (Shenzhen), Sun Yat-sen University, 518107, Shenzhen, China.
Minchao LiSchool of Public Health (Shenzhen), Sun Yat-sen University, 518107, Shenzhen, China.
Huanle LuoSchool of Public Health (Shenzhen), Sun Yat-sen University, 518107, Shenzhen, China.ORCID http://orcid.org/0000-0002-0367-6888
Caijun SunSchool of Public Health (Shenzhen), Sun Yat-sen University, 518107, Shenzhen, China. suncaijun@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-2000-7053
Huacheng YanCenter for Disease Control and Prevention of Southern Military Theatre, 510610, Guangzhou, China. watshing@126.com.
Yuelong ShuSchool of Public Health (Shenzhen), Sun Yat-sen University, 518107, Shenzhen, China. shuylong@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0001-9279-0916
Sun Yat-sen University · CNGuangzhou Center for Disease Control and Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of a universal influenza vaccine to elicit broad immune responses is essential in reducing disease burden and pandemic impact. In this study, the mosaic vaccine design strategy and genetic algorithms were utilized to optimize the seasonal influenza A virus (H1N1, H3N2) hemagglutinin (HA) and neuraminidase (NA) antigens, which also contain most potential T-cell epitopes. These mosaic immunogens were then expressed as virus-like particles (VLPs) using the baculovirus expression system. The immunogenicity and protection effectiveness of the mosaic VLPs were compared to the commercial quadrivalent inactivated influenza vaccine (QIV) in the mice model. Strong cross-reactive antibody responses were observed in mice following two doses of vaccination with the mosaic VLPs, with HI titers higher than 40 in 15 of 16 tested strains as opposed to limited cross HI antibody levels with QIV vaccination. After a single vaccination, mice also show a stronger level of cross-reactive antibody responses than the QIV. The QIV vaccinations only elicited NI antibodies to a small number of vaccine strains, and not even strong NI antibodies to its corresponding vaccine components. In contrast, the mosaic VLPs caused robust NI antibodies to all tested seasonal influenza virus vaccine strains. Here, we demonstrated the mosaic vaccines induces stronger cross-reactive antibodies and robust more T-cell responses compared to the QIV. The mosaic VLPs also provided protection against challenges with ancestral influenza A viruses of both H1 and H3 subtypes. These findings indicated that the mosaic VLPs were a promising strategy for developing a broad influenza vaccine in future.

Identifiers

PMID37679361
PMCPMC10485063
OpenAlexW4386526449

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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.