Evidence map›Paper›PMID 40251181›Full record

ArticleNPJ vaccines2025

Intranasal spike and nucleoprotein fusion protein-based vaccine provides cross-protection and reduced transmission against SARS-CoV-2 variants.

Zineb Lakhrif, Agathe Poupée-Beaugé, Fanny Boursin, Céline Ducournau, Louis Lantier, Nathalie Moiré, Rodolphe Carpentier, Christelle Rossignol, Marianne Maquart, Fabienne Jospin and 18 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

28 authors.

Zineb LakhrifBioMAP, UMR ISP1282 INRAe-Université, Tours, France.
Agathe Poupée-BeaugéBioMAP, UMR ISP1282 INRAe-Université, Tours, France.
Fanny BoursinBioMAP, UMR ISP1282 INRAe-Université, Tours, France.ORCID http://orcid.org/0000-0002-8610-1122
Céline DucournauBioMAP, UMR ISP1282 INRAe-Université, Tours, France.ORCID http://orcid.org/0000-0002-0920-2392
Louis LantierBioMAP, UMR ISP1282 INRAe-Université, Tours, France.
Nathalie MoiréBioMAP, UMR ISP1282 INRAe-Université, Tours, France.
Rodolphe CarpentierUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, France.
Christelle RossignolINRAe, Université de Tours, ISP, Nouzilly, France.
Marianne MaquartMAVIVH, INSERM U1259, Université de Tours, Tours, France.
Fabienne JospinCIRI, Centre International de Recherche en Infectiologie, GIMAP team, Université de Lyon, Inserm, Université Claude Bernard, ENS Lyon, France.
Laetitia MeratINRAE, UE-1277 Plateforme d'Infectiologie Expérimentale (PFIE), Centre de Recherche Val de Loire, Nouzilly, France.
Mireille Caul-FutyEpithelix Sarl, 18 Chemin des Aulx, Plan-les-Ouates, Geneva, Switzerland.
Yazdan YazdanpanahANRS|Emerging Infectious Diseases/Inserm, Paris, France. Service de Maladies Infectieuses et Tropicales, Hôpital Bichat, AP-HP, Paris, France.
Amel BouakaneANRS|Emerging Infectious Diseases/Inserm, Paris, France.
Mickael RiouINRAE, UE-1277 Plateforme d'Infectiologie Expérimentale (PFIE), Centre de Recherche Val de Loire, Nouzilly, France.
Antoine TouzéBiologie des infections à Polyomavirus team, UMR ISP1282 INRAe-Université, Tours, France.
Jean-François EléouëtUnité de Virologie et Immunologie Moléculaires, INRAe, Université Paris Saclay, Jouy en Josas, France.
Charles-Adrien RichardUnité de Virologie et Immunologie Moléculaires, INRAe, Université Paris Saclay, Jouy en Josas, France.ORCID http://orcid.org/0000-0001-5306-2297
François HelleAgents infectieux résistance et chimiothérapie Research Unit, UR4294, Jules Verne University of Picardie, Amiens, France.ORCID http://orcid.org/0000-0001-6884-2456
Sophie Le PoderUMR VIROLOGIE, INRAE, Ecole Nationale Vétérinaire d'Alfort, ANSES, Laboratoire de santé animale, Université Paris-Est, Maisons-Alfort, France.
Bernard KlonjkowskiUMR VIROLOGIE, INRAE, Ecole Nationale Vétérinaire d'Alfort, ANSES, Laboratoire de santé animale, Université Paris-Est, Maisons-Alfort, France.ORCID http://orcid.org/0000-0003-3372-0656
Nicolas MeunierUMR VIROLOGIE, INRAE, Ecole Nationale Vétérinaire d'Alfort, ANSES, Laboratoire de santé animale, Université Paris-Est, Maisons-Alfort, France.
Stéphan ZientaraUMR VIROLOGIE, INRAE, Ecole Nationale Vétérinaire d'Alfort, ANSES, Laboratoire de santé animale, Université Paris-Est, Maisons-Alfort, France.
Stéphane PaulCIRI, Centre International de Recherche en Infectiologie, GIMAP team, Université de Lyon, Inserm, Université Claude Bernard, ENS Lyon, France.ORCID http://orcid.org/0000-0002-8830-4273
Marie-Noëlle MévélecBioMAP, UMR ISP1282 INRAe-Université, Tours, France.
Nicolas Aubrey *BioMAP, UMR ISP1282 INRAe-Université, Tours, France.
Mathieu Epardaud *BioMAP, UMR ISP1282 INRAe-Université, Tours, France. mathieu.epardaud@inrae.fr.
Isabelle Dimier-Poisson *BioMAP, UMR ISP1282 INRAe-Université, Tours, France. isabelle.poisson@univ-tours.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effectiveness of intramuscular vaccines aimed at preventing severe COVID-19 remains limited due to waning immunity and the emergence of novel variants. Next-generation vaccines are needed for broader protection and blocking virus transmission. Here, we rationally designed an original nasal subunit vaccine composed of a fusion protein (SwFN) made of Wuhan spike and nucleoprotein combined with biocompatible mucosal nanocarriers (Nc). In mouse model, the nasal Nc-SwFN vaccine elicited multivalent serum and mucosal neutralizing antibodies. Robust spike and nucleoprotein cross-reactive immunity against variants was induced with a predominant phenotype of resident memory T cells in the lungs. Moreover, Nc-SwFN led to protective responses against Wuhan and Delta infection in relevant models with an absence of morbidity, mortality, and virus dissemination in the lungs and brain. Finally, Nc-SwFN drastically reduced host-to-host transmission. These promising results underscore the advantages of the nasal Nc-SwFN approach as a broad-spectrum vaccine candidate against current and emerging SARS-CoV-2 variants.

Identifiers

PMID40251181
PMCPMC12008205

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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.