Evidence map›Paper›PMID 41327585›Full record

ArticleMicrobiology and immunology2026

Hydroxypropyl Cellulose Enhances Immune Responses to the Current Seasonal Influenza Vaccine in Mice.

Nantaporn Kaewaroon, Sara Yoshimoto, Luthfi Muawan, Shintaro Shichinohe, Tokiko Watanabe

Abstract read
In one paragraph

Article in Microbiology and immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Nantaporn KaewaroonDepartment of Molecular Virology, Research Institute for Microbial Disease, The University of Osaka, Suita, Osaka, Japan.ORCID https://orcid.org/0009-0005-0974-1811
Sara YoshimotoDepartment of Molecular Virology, Research Institute for Microbial Disease, The University of Osaka, Suita, Osaka, Japan.ORCID https://orcid.org/0009-0002-2020-9437
Luthfi MuawanDepartment of Molecular Virology, Research Institute for Microbial Disease, The University of Osaka, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0002-0945-6616
Shintaro ShichinoheDepartment of Molecular Virology, Research Institute for Microbial Disease, The University of Osaka, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0002-8783-2103
Tokiko WatanabeDepartment of Molecular Virology, Research Institute for Microbial Disease, The University of Osaka, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0001-6461-5379

Funding

This study was supported by JSPS KAKENHI Grants-in-Aid for Scientific Research (B) [JP22H02521 (to Tokiko Watanabe); a Grant-in-Aid for Scientific Research (C) [JP24K09264 (to Shintaro Shichinohe)]; the AMED Research Program on Emerging and Re-emerging Infectious Diseases [JP19fk0108113 (to Tokiko Watanabe)]; AMED under Grant Numbers JP223fa627002, JP22am0401030, JP233fa827018 (to Tokiko Watanabe); AMED Advanced Research and Development Programs for Medical Innovation (AMED-CREST) [JP22gm1610010 (to Tokiko Watanabe)]; and the Takeda Science Foundation (to Tokiko Watanabe).
6 · The paper itself

Abstract

Influenza A and B viruses cause annual epidemics and continue to pose global public health concerns. The most effective approach to preventing or mitigating the severity of influenza is vaccination. Inactivated split influenza HA vaccines are commonly used worldwide due to their strong safety profile and broad range of target groups; however, their efficacy is suboptimal, especially in the elderly. Adjuvants are used to enhance the effectiveness of some influenza vaccines, but few adjuvants have been approved for human vaccines. Previously, we identified hydroxypropyl cellulose as a promising adjuvant for the split influenza HA vaccine for the 2015-2016 and 2016-2017 influenza seasons. Here, we evaluated whether hydroxypropyl cellulose could enhance the efficacy of the quadrivalent split HA vaccine for the 2023-2024 influenza season, which contains the HA proteins of A/Victoria/4897/2022 (H1N1)pdm09 and three other strains. Using a mouse model, we performed immunogenicity studies and assessed protective efficacy against challenges with homologous and heterologous H1N1pdm09 virus strains. We found that hydroxypropyl cellulose in combination with the HA vaccine generated higher virus-specific IgG antibody titers compared to the vaccine alone. The adjuvanted vaccine provided complete protection against homologous challenge and enhanced viral clearance from respiratory organs. Notably, the adjuvanted vaccine demonstrated cross-protective efficacy against heterologous H1N1pdm09 virus challenge, improving survival rates compared to vaccine alone. Our results demonstrate that hydroxypropyl cellulose has potential as an adjuvant for current seasonal influenza vaccines.

Indexed as

Adjuvants, ImmunologicAdjuvants, VaccineCelluloseInfluenza VaccinesOrthomyxoviridae InfectionsAnimalsAntibodies, ViralCross ProtectionDisease Models, AnimalFemaleHemagglutinin Glycoproteins, Influenza VirusHumansImmunoglobulin GInfluenza A Virus, H1N1 SubtypeInfluenza, HumanMiceAdjuvants, ImmunologicAdjuvants, VaccineAntibodies, ViralCelluloseHemagglutinin Glycoproteins, Influenza VirushydroxypropylcelluloseImmunoglobulin GInfluenza VaccinesVaccines, Inactivatedadjuvanthydroxypropyl celluloseseasonal influenza vaccine

Identifiers

PMID41327585
PMCPMC12868939

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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.