Evidence map›Paper›PMID 39285168›Full record

ArticleNPJ vaccines2024

CircRNA based multivalent neuraminidase vaccine induces broad protection against influenza viruses in mice.

Xinyu Yue, Cailing Zhong, Rui Cao, Sizhe Liu, Zhiran Qin, Lin Liu, Yanmei Zhai, Wanyu Luo, Yikai Lian, Mengjie Zhang and 16 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
–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

24 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. mRNA Vaccines for Influenza: Hope for a Universal Vaccine?BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Roles and Applications of Circular RNA in Virus Infection.International journal of molecular sciences · 2025
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article
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

26 authors.

Xinyu Yue *School of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Cailing Zhong *School of Pharmaceutical Sciences, Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Rui Cao *School of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Sizhe Liu *School of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Zhiran QinInstitute of Infectious Disease, Shenzhen Bay Laboratory, Shenzhen, Guangdong, China.
Lin LiuSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Yanmei ZhaiSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Wanyu LuoSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Yikai LianInstitute of Infectious Disease, Shenzhen Bay Laboratory, Shenzhen, Guangdong, China.
Mengjie ZhangInstitute of Infectious Disease, Shenzhen Bay Laboratory, Shenzhen, Guangdong, China.
Hongjie LuSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Yuanyuan WangSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Mengxin XuSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Shuning LiuSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Kexin LvSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Yuzhu SunSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Xingchen ZhuSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Haoting MaiSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.
Jing LiaoGMU-GIBH Joint School of Life Sciences, Guangzhou Medical University, Guangzhou, China.
Jingyi YangVaccine and Immunology Research Center, Translational Medical Research Institute, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Lei DengHunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha, China.
Yang LiuInstitute of Infectious Disease, Shenzhen Bay Laboratory, Shenzhen, Guangdong, China.
Caijun SunSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China.ORCID http://orcid.org/0000-0002-2000-7053
Ke-Wei ZhengSchool of Biomedical Sciences, Hunan University, Changsha, China. zhengkewei@hnu.edu.cn.ORCID http://orcid.org/0000-0002-4110-4776
Yuelong ShuSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China. shuylong@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0001-9279-0916
Yao-Qing ChenSchool of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-Sen University, Shenzhen, China. chenyaoqing@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-4659-1550

Funding

National Natural Science Foundation of China (National Science Foundation of China) 31970881, 92169104
6 · The paper itself

Abstract

Developing broad-spectrum influenza vaccines is crucial for influenza control and potential pandemic preparedness. Here, we reported a novel vaccine design utilizing circular RNA (circRNA) as a delivery platform for multi-subtype neuraminidases (NA) (influenza A N1, N2, and influenza B Victoria lineage NA) immunogens. Individual NA circRNA lipid nanoparticles (LNP) elicited robust NA-specific antibody responses with neuraminidase inhibition activity (NAI), preventing the virus from egressing and infecting neighboring cells. Additionally, the administration of circRNA LNP induced cellular immunity in mice. To achieve a universal influenza vaccine, we combined all three subtypes of NA circRNA-LNPs to generate a trivalent circRNA vaccine. The trivalent vaccine elicited a balanced antibody response against all three NA subtypes and a Th1-biased immune response in mice. Moreover, it protected mice against the lethal challenge of matched and mismatched H1N1, H3N2, and influenza B viruses, encompassing circulating and ancestral influenza virus strains. This study highlights the potential of delivering multiple NA antigens through circRNA-LNPs as a promising strategy for effectively developing a universal influenza vaccine against diverse influenza viruses.

Identifiers

PMID39285168
PMCPMC11405689

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.