Evidence map›Paper›PMID 39394212›Full record

ArticleNPJ vaccines2024

Recombinant RSV G protein vaccine induces enhanced respiratory disease via IL-13 and mucin overproduction.

Eigo Kawahara, Kota Senpuku, Yoshino Kawaguchi, Shinya Yamamoto, Koubun Yasuda, Etsushi Kuroda, Noriko Ouji-Sageshima, Toshihiro Ito, Toshiro Hirai, Takehiko Shibata and 1 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Article
  10. Early Origins of Asthma and Allergies: Clues From Studies in China.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2025
    Review
  11. Review
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

11 authors.

Eigo KawaharaLaboratory of Nano-Design for Innovative Drug Development, Graduate School of Pharmaceutical Sciences, Osaka University, Osaka, Japan.
Kota SenpukuLaboratory of Nano-Design for Innovative Drug Development, Graduate School of Pharmaceutical Sciences, Osaka University, Osaka, Japan.
Yoshino KawaguchiVaccine Creation Group, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Shinya YamamotoThe Research Foundation for Microbial Diseases of Osaka University, Osaka, Japan.
Koubun YasudaDepartment of Immunology, Hyogo College of Medicine, Hyogo, Japan.
Etsushi KurodaDepartment of Immunology, Hyogo College of Medicine, Hyogo, Japan.
Noriko Ouji-SageshimaDepartment of Immunology, Nara Medical University, Nara, Japan.
Toshihiro ItoDepartment of Immunology, Nara Medical University, Nara, Japan.
Toshiro HiraiLaboratory of Nano-Design for Innovative Drug Development, Graduate School of Pharmaceutical Sciences, Osaka University, Osaka, Japan.ORCID http://orcid.org/0000-0002-9212-1664
Takehiko ShibataDepartment of Microbiology, Tokyo Medical University, Tokyo, Japan.
Yasuo YoshiokaLaboratory of Nano-Design for Innovative Drug Development, Graduate School of Pharmaceutical Sciences, Osaka University, Osaka, Japan. y-yoshioka@biken.osaka-u.ac.jp.ORCID http://orcid.org/0000-0002-7265-9221

Funding

Japan Agency for Medical Research and Development (AMED) 243fa727001h0003Japan Agency for Medical Research and Development (AMED) JP223fa627002MEXT | Japan Science and Technology Agency (JST) JPMJSP2138MEXT | Japan Society for the Promotion of Science (JSPS) 23H02652
6 · The paper itself

Abstract

The G protein expressed on the surface of respiratory syncytial virus (RSV) is important for adhesion to host cells and as a vaccine target antigen. The corresponding vaccines can effectively eliminate RSV. However, they exacerbate pulmonary immunopathology including eosinophilic infiltration in the lungs after an RSV challenge in animal models, raising concerns about enhanced respiratory disease (ERD); thus, approaches that mitigate these effects are urgently needed. Herein, we aimed to examine the mechanisms of G protein vaccine-induced ERD in mice, using recombinant G protein as a vaccine antigen. After the RSV challenge, G protein-vaccinated mice exhibited lung weight gain, lung tissue damage, and increased infiltration of eosinophils, neutrophils, and CD4

Identifiers

PMID39394212
PMCPMC11470036

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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.