Evidence map›Paper›PMID 36560407›Full record

ArticleVaccines2022

Immunogenicity and Efficacy of Monovalent and Bivalent Formulations of a Virus-Like Particle Vaccine against SARS-CoV-2.

Matthew D Resch, Ke Wen, Ryan Mazboudi, Hannah Mulhall Maasz, Mirjana Persaud, Kaitlyn Garvey, Leslie Gallardo, Paul Gottlieb, Aleksandra Alimova, Reza Khayat and 4 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. 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

14 authors at 4 institutions in 2 countries.

Matthew D ReschTechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY 10523, USA.ORCID 0000-0001-5346-3023
Ke WenTechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY 10523, USA.
Ryan MazboudiTechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY 10523, USA.
Hannah Mulhall MaaszTechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY 10523, USA.
Mirjana PersaudTechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY 10523, USA.
Kaitlyn GarveyTechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY 10523, USA.
Leslie GallardoTechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY 10523, USA.
Paul GottliebCUNY School of Medicine, The City College of New York, New York, NY 10031, USA.ORCID 0000-0002-1963-2732
Aleksandra AlimovaCUNY School of Medicine, The City College of New York, New York, NY 10031, USA.
Reza KhayatDepartment of Chemistry and Biochemistry, The City College of New York, New York, NY 10031, USA.ORCID 0000-0001-6601-2184
Jorge MoralesMicroscopy Facility, Division of Science, The City College of New York, New York, NY 10031, USA.
Helle Bielefeldt-OhmannSchool of Chemistry and Molecular Biosciences, University of Queensland, St. Lucia, QLD 4072, Australia.
Richard A BowenDepartment of Biomedical Sciences, Colorado State University, Fort Collins, CO 80521, USA.
Jose M GalarzaTechnoVax, Inc., 6 Westchester Plaza, Elmsford, NY 10523, USA.
TechnoVax (United States) · USCity College of New York · USColorado State University · USThe University of Queensland · AU

Funding

Universal VLP-Based Flu Vaccine:Broadly protective (universal) virus-like particle (VLP) based influenza vaccine that can neutralize a broad spectrum of influenza A virus subtypes.R44AI106145 · NIAID · TECHNOVAX, INC. · PI GALARZA, JOSE M. · 2018 to 2019
$1.5M
NIAID NIH HHS R44 AI106145
6 · The paper itself

Abstract

Virus-like particles (VLPs) offer great potential as a safe and effective vaccine platform against SARS-CoV-2, the causative agent of COVID-19. Here, we show that SARS-CoV-2 VLPs can be generated by expression of the four viral structural proteins in a mammalian expression system. Immunization of mice with a monovalent VLP vaccine elicited a potent humoral response, showing neutralizing activity against multiple variants of SARS-CoV-2. Subsequent immunogenicity and efficacy studies were performed in the Golden Syrian hamster model, which closely resembles the pathology and progression of COVID-19 in humans. Hamsters immunized with a bivalent VLP vaccine were significantly protected from infection with the Beta or Delta variant of SARS-CoV-2. Vaccinated hamsters showed reduced viral load, shedding, replication, and pathology in the respiratory tract. Immunized hamsters also showed variable levels of cross-neutralizing activity against the Omicron variant. Overall, the VLP vaccine elicited robust protective efficacy against SARS-CoV-2. These promising results warrant further study of multivalent VLP vaccines in Phase I clinical trials in humans.

Indexed as

protective efficacySARS-CoV-2vaccinevirus-like particleVLP

Identifiers

PMID36560407
PMCPMC9782034
OpenAlexW4309855223

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.