Evidence map›Paper›PMID 40338109›Full record

ArticleInfluenza and other respiratory viruses2025

Evaluating Bacillus Calmette-Guérin Polysaccharide Nucleic Acid as an Adjuvant for Influenza Vaccines in Mice.

Sijing Yan, Fan Yang, Jia Ji, Xiantian Lin, Ping Wang, Han Wu, Linfang Cheng, Fumin Liu, Nanping Wu, Hangping Yao and 2 more

Abstract read
In one paragraph

Article in Influenza and other respiratory viruses, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Sijing YanState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Fan YangState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Jia JiState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Xiantian LinState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Ping WangState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Han WuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Linfang ChengState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Fumin LiuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Nanping WuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Hangping YaoState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Wade S J WuAdvin Biotech, Inc., San Diego, California, USA.
Haibo WuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.ORCID 0000-0001-5550-5186

Funding

National Science Foundation of the People's Republic of China 32273092Zhejiang Provincial Natural Science Foundation of China LY24H190001
6 · The paper itself

Abstract

backgroundTo enhance influenza vaccine efficacy, it is essential to investigate new adjuvants that are both safe and effective. In a recent study utilizing a mouse model, Bacillus Calmette-Guérin polysaccharide nucleic acid (BCG-PSN) emerged as a promising candidate vaccine adjuvant.

methodsThis study evaluated the immunomodulatory effects of BCG-PSN on influenza vaccines hemagglutinin antigen and aluminum adjuvant as controls. Mice were immunized with H1N1 antigen and adjuvants, and serum antibody levels were measured using hemagglutination inhibition, enzyme-linked immunosorbent assay, and microneutralization assays. Flow cytometry and enzyme-linked immunospot assays assessed T cell phenotypes and cytokine expression. The protective effects were tested through challenge experiments, and the adjuvants were further evaluated in a quadrivalent seasonal influenza vaccine.

resultsBCG-PSN adjuvant exhibited favorable safety profiles and demonstrated an ability to elevate total antibody titers, particularly enhancing neutralizing antibody production when co-administered with the H1N1 antigen. BCG-PSN increased cytokine levels and the proportion of CD8+ T lymphocytes, indicating its capacity to enhance cellular immunity. Upon viral challenge in mice, BCG-PSN mitigated the production of inflammatory factors and reduced lung pathology, effectively protecting the mice. Furthermore, BCG-PSN displayed heightened immunogenicity against a mixture of four antigens.

conclusionsBCG-PSN is a reliable and efficient adjuvant for influenza vaccines, holding promise for enhancing vaccine efficacy and increasing immune responses.

Indexed as

Adjuvants, ImmunologicInfluenza VaccinesMycobacterium bovisOrthomyxoviridae InfectionsPolysaccharides, BacterialAnimalsAntibodies, NeutralizingAntibodies, ViralBCG VaccineCytokinesFemaleInfluenza A Virus, H1N1 SubtypeMiceMice, Inbred BALB CAdjuvants, ImmunologicAntibodies, NeutralizingAntibodies, ViralBCG VaccineCytokinesInfluenza VaccinesPolysaccharides, BacterialadjuvantBCG polysaccharide nucleic acidcellular immunityhumoral immunityinfluenza vaccine

Identifiers

PMID40338109
PMCPMC12058303

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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.