Evidence map›Paper›PMID 38563763›Full record

ArticleJournal of virology2024

A measles-vectored vaccine candidate expressing prefusion-stabilized SARS-CoV-2 spike protein brought to phase I/II clinical trials: candidate selection in a preclinical murine model.

Jérémy Brunet, Zaineb Choucha, Marion Gransagne, Houda Tabbal, Min-Wen Ku, Julian Buchrieser, Priyanka Fernandes, Damien Batalie, Jodie Lopez, Laurence Ma and 13 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2024. 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
0.4field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  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

23 authors at 4 institutions in 2 countries.

Jérémy Brunet *Institut Pasteur, Université Paris Cité, Département de Santé Globale, Paris, France.
Zaineb Choucha *Institut Pasteur, Université Paris Cité, Département de Santé Globale, Paris, France.
Marion Gransagne *Institut Pasteur, Université Paris Cité, Département de Santé Globale, Paris, France.
Houda TabbalInstitut Pasteur, Université Paris Cité, CNRS UMR3569, Génétique Moléculaire des Virus à ARN, Paris, France.
Min-Wen KuInstitut Pasteur, Université Paris Cité, Pasteur-TheraVectys Joint Lab, Paris, France.
Julian BuchrieserInstitut Pasteur, Université Paris Cité, CNRS UMR3569, Virus and Immunity Unit, Paris, France.
Priyanka FernandesInstitut Pasteur, Université Paris Cité, INSERM U1223, Innate Immunity Unit, Paris, France.
Damien BatalieInstitut Pasteur, Université Paris Cité, CNRS UMR3569, Génétique Moléculaire des Virus à ARN, Paris, France.
Jodie LopezInstitut Pasteur, Université Paris Cité, Pasteur-TheraVectys Joint Lab, Paris, France.
Laurence MaInstitut Pasteur, Université Paris Cité, Biomics, C2RT, Paris, France.
Evelyne DufourInstitut Pasteur, Université Paris Cité, CNRS UMR 3528, Production and Purification of Recombinant Proteins Technological Platform, Paris, France.
Emeline SimonInstitut Pasteur, Université Paris Cité, CNRS UMR3569, Génétique Moléculaire des Virus à ARN, Paris, France.
David HardyInstitut Pasteur, Université Paris Cité, Histopathology Platform, Paris, France.
Stéphane PetresInstitut Pasteur, Université Paris Cité, CNRS UMR 3528, Production and Purification of Recombinant Proteins Technological Platform, Paris, France.
Françoise GuinetInstitut Pasteur, Université Paris Cité, INSERM U1223, Lymphocytes and Immunity Unit, Paris, France.
Helene Strick-MarchandInstitut Pasteur, Université Paris Cité, INSERM U1223, Innate Immunity Unit, Paris, France.
Marc MonotInstitut Pasteur, Université Paris Cité, Biomics, C2RT, Paris, France.
Pierre CharneauInstitut Pasteur, Université Paris Cité, Pasteur-TheraVectys Joint Lab, Paris, France.
Laleh MajlessiInstitut Pasteur, Université Paris Cité, Pasteur-TheraVectys Joint Lab, Paris, France.
W Paul DuprexCenter for Vaccine Research, Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0003-1716-6376
Christiane Gerke *Institut Pasteur, Université Paris Cité, Innovation Office, Vaccine Programs, Paris, France.ORCID 0000-0001-9446-8031
Annette Martin *Institut Pasteur, Université Paris Cité, CNRS UMR3569, Génétique Moléculaire des Virus à ARN, Paris, France.ORCID 0000-0002-3054-3925
Nicolas Escriou *Institut Pasteur, Université Paris Cité, Département de Santé Globale, Paris, France.ORCID 0000-0002-1224-6839
Institut Pasteur · FRCentre National de la Recherche Scientifique · FRInserm · FRUniversity of Pittsburgh · US

Funding

Practices CoreUC7AI180311 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI William Paul Duprex · 2023 to 2026
$13.2M
Agence Nationale de la Recherche (ANR) 2 post-doctoral fellowshipsCoalition for Epidemic Preparedness Innovations (CEPI) Outbreak Response to Novel Coronavirus (COVID-19): Development of a vaccine against novel coronavirus SARS-CoV-2 using the clinical Phase III measles vector technologyEC | Horizon 2020 Framework Programme (H2020) 101003589 (post-doctoral fellowship)Institut Pasteur URGENCE COVID-19NIAID NIH HHS UC7 AI180311Université Sorbonne Paris Cité (USPC) doctoral fellowship
6 · The paper itself

Abstract

In the early COVID-19 pandemic with urgent need for countermeasures, we aimed at developing a replicating viral vaccine using the highly efficacious measles vaccine as vector, a promising technology with prior clinical proof of concept. Building on our successful pre-clinical development of a measles virus (MV)-based vaccine candidate against the related SARS-CoV, we evaluated several recombinant MV expressing codon-optimized SARS-CoV-2 spike glycoprotein. Candidate V591 expressing a prefusion-stabilized spike through introduction of two proline residues in HR1 hinge loop, together with deleted S1/S2 furin cleavage site and additional inactivation of the endoplasmic reticulum retrieval signal, was the most potent in eliciting neutralizing antibodies in mice. After single immunization, V591 induced similar neutralization titers as observed in sera of convalescent patients. The cellular immune response was confirmed to be Th1 skewed. V591 conferred long-lasting protection against SARS-CoV-2 challenge in a murine model with marked decrease in viral RNA load, absence of detectable infectious virus loads, and reduced lesions in the lungs. V591 was furthermore efficacious in an established non-human primate model of disease (see companion article [S. Nambulli, N. Escriou, L. J. Rennick, M. J. Demers, N. L. Tilston-Lunel et al., J Virol 98:e01762-23, 2024, https://doi.org/10.1128/jvi.01762-23]). Thus, V591 was taken forward into phase I/II clinical trials in August 2020. Unexpected low immunogenicity in humans (O. Launay, C. Artaud, M. Lachâtre, M. Ait-Ahmed, J. Klein et al., eBioMedicine 75:103810, 2022, https://doi.org/10.1016/j.ebiom.2021.103810) revealed that the underlying mechanisms for resistance or sensitivity to pre-existing anti-measles immunity are not yet understood. Different hypotheses are discussed here, which will be important to investigate for further development of the measles-vectored vaccine platform.IMPORTANCESARS-CoV-2 emerged at the end of 2019 and rapidly spread worldwide causing the COVID-19 pandemic that urgently called for vaccines. We developed a vaccine candidate using the highly efficacious measles vaccine as vector, a technology which has proved highly promising in clinical trials for other pathogens. We report here and in the companion article by Nambulli et al. (J Virol 98:e01762-23, 2024, https://doi.org/10.1128/jvi.01762-23) the design, selection, and preclinical efficacy of the V591 vaccine candidate that was moved into clinical development in August 2020, 7 months after the identification of SARS-CoV-2 in Wuhan. These unique in-human trials of a measles vector-based COVID-19 vaccine revealed insufficient immunogenicity, which may be the consequence of previous exposure to the pediatric measles vaccine. The three studies together in mice, primates, and humans provide a unique insight into the measles-vectored vaccine platform, raising potential limitations of surrogate preclinical models and calling for further refinement of the platform.

Indexed as

COVID-19 VaccinesMeasles virusSARS-CoV-2Spike Glycoprotein, CoronavirusAnimalsAntibodies, NeutralizingAntibodies, ViralCOVID-19Disease Models, AnimalFemaleGenetic VectorsHumansMeasles VaccineMiceMice, Inbred BALB CAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesMeasles VaccineSpike Glycoprotein, CoronavirusCOVID-19 vaccinemeasles vectorprefusion-stabilized spikevectored vaccine

Identifiers

PMID38563763
PMCPMC11210269
OpenAlexW4393411453

What Socratic holds

Textmetadata
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 Socratic graph.