Evidence map›Paper›PMID 41221175›Full record

ArticleClinical and experimental vaccine research2025

Cholera toxin B subunit fusion enhances the immunogenicity of the H5 stem domain against the H5N2 avian influenza virus.

Chan Lee, Seongjae Kim, Jinseon You, Minjeong Seo, Youngbin Kim, Jeongdon Park, Hye-Won Park, Jaerang Rho

Abstract read
In one paragraph

Article in Clinical and experimental vaccine research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

8 authors.

Chan LeeDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Korea.ORCID https://orcid.org/0000-0003-0164-023X
Seongjae KimDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Korea.ORCID https://orcid.org/0009-0003-7469-1211
Jinseon YouDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Korea.ORCID https://orcid.org/0000-0001-9602-2519
Minjeong SeoDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Korea.ORCID https://orcid.org/0009-0001-7333-2327
Youngbin KimDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Korea.ORCID https://orcid.org/0009-0007-2997-1838
Jeongdon ParkDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Korea.ORCID https://orcid.org/0009-0002-9502-1754
Hye-Won ParkDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Korea.ORCID https://orcid.org/0000-0002-0566-0636
Jaerang RhoDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Korea.ORCID https://orcid.org/0000-0002-0019-4939

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The development of a universal avian influenza vaccine remains a critical issue for both the global public health and poultry industries. The hemagglutinin (H) stem/stalk region of highly pathogenic avian influenza viruses (HPAIVs) is capable of inducing broadly neutralizing antibodies but is limited by its poor immunogenicity. Materials and Methods: To increase the immunogenicity of the stem domain, we engineered a recombinant fusion construct consisting of the stem domain of the H5 subtype and the nontoxic cholera toxin B subunit (CTB), a well-characterized mucosal adjuvant and immunomodulator. C57BL/6 mice were immunized intraperitoneally with the CTB-H5 stem fusion protein. Humoral immune responses and virus-neutralizing activities were subsequently assessed. Results: Mice immunized with CTB-H5 stem fusion protein developed significantly higher serum immunoglobulin G titers and increased binding affinity to the native trimeric H5 antigen. Sera from the CTB-H5 stem group demonstrated enhanced virus-neutralizing activity in plaque reduction assays against the H5N2 virus. These results suggest that CTB fusion significantly enhances the immunogenicity and protective potential of the conserved H5 stem domain against the H5N2 virus. Conclusion: These findings support the use of CTB as an effective adjuvant platform for the development of stem-based influenza vaccines targeting HPAIVs.

Indexed as

Avian influenzaCholera toxinHemagglutininInfluenza vaccineVaccine adjuvant

Identifiers

PMID41221175
PMCPMC12599431

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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.