Evidence map›Paper›PMID 38378856›Full record

ArticleScientific reports2024

Immunogenicity and protective efficacy of a co-formulated two-in-one inactivated whole virus particle COVID-19/influenza vaccine.

Chimuka Handabile, Marumi Ohno, Toshiki Sekiya, Naoki Nomura, Tomomi Kawakita, Mamiko Kawahara, Masafumi Endo, Tomohiro Nishimura, Minako Okumura, Shinsuke Toba and 11 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.3field-weighted citation impact, top 13% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Understanding and controlling pandemic influenza.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2026
    Review
  3. Review
  4. 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

21 authors at 6 institutions in 2 countries.

Chimuka HandabileInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Marumi OhnoInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Toshiki SekiyaInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Naoki NomuraInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Tomomi KawakitaInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Mamiko KawaharaDivision of Biologics Development, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Masafumi EndoKM Biologics Co. Ltd, Kumamoto, Japan.
Tomohiro NishimuraKM Biologics Co. Ltd, Kumamoto, Japan.
Minako OkumuraKM Biologics Co. Ltd, Kumamoto, Japan.
Shinsuke TobaShionogi Pharmaceutical Research Center, Shionogi & Company, Limited, Toyonaka, Japan.
Michihito SasakiInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Yasuko OrbaInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Brendon Y ChuaInternational Collaboration Unit, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Louise C RowntreeDepartment of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Thi H O NguyenDepartment of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Masashi ShingaiInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Akihiko SatoInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Hirofumi SawaInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Kazumasa OgasawaraDivision of Biologics Development, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Katherine KedzierskaInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
Hiroshi KidaInstitute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan. kida@vetmed.hokudai.ac.jp.
Hokkaido University · JPKM Biologics (Japan) · JPPeter Doherty Institute · AUFutaba (Japan) · JPShionogi (Japan) · JPUniversity of Melbourne · AU

Funding

Australian National Health and Medical Research Council #1173871Australian National Health and Medical Research Council #1194036Japan Agency for Medical Research and Development JP223fa627005Japan Agency for Medical Research and Development JP23wm0125008JSPS 21H02376JSPS 22K15483JSPS 23K15362Ministry of Education, Culture, Sports, Science and Technology 1801
6 · The paper itself

Abstract

Due to the synchronous circulation of seasonal influenza viruses and severe acute respiratory coronavirus 2 (SARS-CoV-2) which causes coronavirus disease 2019 (COVID-19), there is need for routine vaccination for both COVID-19 and influenza to reduce disease severity. Here, we prepared individual WPVs composed of formalin-inactivated SARS-CoV-2 WK 521 (Ancestral strain; Co WPV) or influenza virus [A/California/07/2009 (X-179A) (H1N1) pdm; Flu WPV] to produce a two-in-one Co/Flu WPV. Serum analysis from vaccinated mice revealed that a single dose of Co/Flu WPV induced antigen-specific neutralizing antibodies against both viruses, similar to those induced by either type of WPV alone. Following infection with either virus, mice vaccinated with Co/Flu WPV showed no weight loss, reduced pneumonia and viral titers in the lung, and lower gene expression of proinflammatory cytokines, as observed with individual WPV-vaccinated. Furthermore, a pentavalent vaccine (Co/qFlu WPV) comprising of Co WPV and quadrivalent influenza vaccine (qFlu WPV) was immunogenic and protected animals from severe COVID-19. These results suggest that a single dose of the two-in-one WPV provides efficient protection against SARS-CoV-2 and influenza virus infections with no evidence of vaccine interference in mice. We propose that concomitant vaccination with the two-in-one WPV can be useful for controlling both diseases.

Indexed as

COVID-19Influenza A Virus, H1N1 SubtypeInfluenza, HumanInfluenza VaccinesAnimalsAntibodies, ViralCOVID-19 VaccinesHumansImmunogenicity, VaccineMiceSARS-CoV-2VaccinationVirionAntibodies, ViralCOVID-19 VaccinesInfluenza Vaccines

Identifiers

PMID38378856
PMCPMC10879490
OpenAlexW4391970863

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.