Evidence map›Paper›PMID 36371408›Full record

Trial reportNature communications2022

Durability and cross-reactivity of immune responses induced by a plant-based virus-like particle vaccine for COVID-19.

Philipe Gobeil, Stéphane Pillet, Iohann Boulay, Nathalie Charland, Aurélien Lorin, Matthew P Cheng, Donald C Vinh, Philippe Boutet, Robbert Van Der Most, François Roman and 4 more

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04450004 (A Randomized, Partially-Blinded, Dose-Ranging Phase 1 Study to Assess the Safety, Tolerability, and Immunogenicity of a Recombinant Coronavirus-Like Particle COVID 19 Vaccine in Adults 18-55 Years of Age), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

NCT04450004 phase1completednot on this map

A Randomized, Partially-Blinded, Dose-Ranging Phase 1 Study to Assess the Safety, Tolerability, and Immunogenicity of a Recombinant Coronavirus-Like Particle COVID 19 Vaccine in Adults 18-55 Years of Age

TypeinterventionalSponsorMedicagoRan2020 to 2021Enrolled180ConditionsSARS-CoV 2ArmsIntramuscular Vaccine
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Advanced Materials for SARS-CoV-2 Vaccines.Advanced materials (Deerfield Beach, Fla.) · 2022
    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

14 authors.

Philipe GobeilMedicago Inc., Suite 600, 1020 route de l'Église, Québec, QC, G1V 3V9, Canada.
Stéphane PilletMedicago Inc., Suite 600, 1020 route de l'Église, Québec, QC, G1V 3V9, Canada.
Iohann BoulayMedicago Inc., Suite 600, 1020 route de l'Église, Québec, QC, G1V 3V9, Canada.
Nathalie CharlandMedicago Inc., Suite 600, 1020 route de l'Église, Québec, QC, G1V 3V9, Canada.
Aurélien LorinMedicago Inc., Suite 600, 1020 route de l'Église, Québec, QC, G1V 3V9, Canada.
Matthew P ChengThe Research Institute of the McGill University Health Centre, 1001 Decarie Street, Montreal, QC, H4A 3J1, Canada.
Donald C VinhThe Research Institute of the McGill University Health Centre, 1001 Decarie Street, Montreal, QC, H4A 3J1, Canada.ORCID 0000-0003-1347-7767
Philippe BoutetGlaxoSmithKline (Vaccines), Avenue Fleming 20, 1300, Wavre, Belgium.
Robbert Van Der MostGlaxoSmithKline (Vaccines), rue de l'Institut 89, 1330, Rixensart, Belgium.ORCID 0000-0002-3065-6946
François RomanGlaxoSmithKline (Vaccines), Avenue Fleming 20, 1300, Wavre, Belgium.
Maria Angeles CeregidoGlaxoSmithKline (Vaccines), Avenue Fleming 20, 1300, Wavre, Belgium.
Nathalie LandryMedicago Inc., Suite 600, 1020 route de l'Église, Québec, QC, G1V 3V9, Canada.
Marc-André D'AoustMedicago Inc., Suite 600, 1020 route de l'Église, Québec, QC, G1V 3V9, Canada.
Brian J WardMedicago Inc., Suite 600, 1020 route de l'Église, Québec, QC, G1V 3V9, Canada. wardb@medicago.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the SARS-CoV-2 pandemic evolves, vaccine evaluation needs to include consideration of both durability and cross-reactivity. This report expands on previously reported results from a Phase 1 trial of an AS03-adjuvanted, plant-based coronavirus-like particle (CoVLP) displaying the spike (S) glycoprotein of the ancestral SARS-CoV-2 virus in healthy adults (NCT04450004). Humoral and cellular responses against the ancestral strain were evaluated 6 months post-second dose (D201) as secondary outcomes. Independent of dose, all vaccinated individuals retain binding antibodies, and ~95% retain neutralizing antibodies (NAb). Interferon gamma and interleukin-4 responses remain detectable in ~94% and ~92% of vaccinees respectively. In post-hoc analyses, variant-specific (Alpha, Beta, Delta, Gamma and Omicron) NAb were assessed at D42 and D201. Using a live virus neutralization assay, broad cross-reactivity is detectable against all variants at D42. At D201, cross-reactive antibodies are detectable in almost all participants against Alpha, Gamma and Delta variants (94%) and the Beta variant (83%) and in a smaller proportion against Omicron (44%). Results are similar with the pseudovirion assay. These data suggest that two doses of 3.75 µg CoVLP+AS03 elicit a durable and cross-reactive response that persists for at least 6 months post-vaccination.

Indexed as

COVID-19Vaccines, Virus-Like ParticleViral VaccinesAdultAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesHumansImmunitySARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccines, Virus-Like ParticleViral Vaccines

Identifiers

PMID36371408
PMCPMC9653456

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.