Evidence map›Paper›PMID 34492082›Full record

ArticlePLoS pathogens2021

Novel virus-like nanoparticle vaccine effectively protects animal model from SARS-CoV-2 infection.

Qibin Geng, Wanbo Tai, Victoria K Baxter, Juan Shi, Yushun Wan, Xiujuan Zhang, Stephanie A Montgomery, Sharon A Taft-Benz, Elizabeth J Anderson, Audrey C Knight and 11 more

Abstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

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  15. Structural basis for mouse receptor recognition by bat SARS2-like coronaviruses.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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.

Qibin GengDepartment of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, Minnesota, United States of America.ORCID 0000-0003-4872-2400
Wanbo TaiLaboratory of Viral Immunology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
Victoria K BaxterDepartment of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.ORCID 0000-0003-0916-360X
Juan ShiLaboratory of Viral Immunology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
Yushun WanDepartment of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, Minnesota, United States of America.
Xiujuan ZhangLaboratory of Viral Immunology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.ORCID 0000-0002-5312-0909
Stephanie A MontgomeryDepartment of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.ORCID 0000-0001-8012-5302
Sharon A Taft-BenzDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Elizabeth J AndersonDivision of Comparative Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.ORCID 0000-0001-7877-1639
Audrey C KnightDivision of Comparative Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.ORCID 0000-0002-8009-8081
Kenneth H DinnonDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, United States of America.ORCID 0000-0002-8942-1551
Sarah R LeistRapidly Emerging Antiviral Drug Development Initiative, University of North Carolina, Chapel Hill, North Carolina, United States of America.ORCID 0000-0002-4989-5381
Ralph S BaricDivision of Comparative Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Jian ShangDepartment of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, Minnesota, United States of America.
Sung-Wook HongCenter for Immunology, Department of Microbiology and Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID 0000-0001-9718-726X
Aleksandra DrelichDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.
Chien-Te K TsengDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0001-5726-9834
Marc JenkinsCenter for Immunology, Department of Microbiology and Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.
Mark HeiseDivision of Comparative Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.ORCID 0000-0001-5829-8477
Lanying DuLaboratory of Viral Immunology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
Fang LiDepartment of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, Minnesota, United States of America.ORCID 0000-0002-1958-366X

Funding

Mechanisms of MERS-CoV Entry, Cross-species Transmission and PathogenesisR01AI110700 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BARIC, RALPH S, LI, FANG · 2015 to 2024
$7.4M
Respiratory Virus Vaccine and Adjuvant Exploration - Equipment SupplementU01AI149644 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BARIC, RALPH S · 2019 to 2023
$6.1M
INFECTIOUS DISEASE PATHOGENESIS TRAININGT32AI007151 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JULIANO, JONATHAN J · 1985 to 2024
$5.5M
Molecular Biology of Viral Diseases Predoctoral Training GrantT32AI007419 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Mark T Heise, CARY A MOODY · 1993 to 2026
$4.7M
Receptor recognition mechanisms of coronavirusesR01AI089728 · NIAID · UNIVERSITY OF MINNESOTA · PI Fang Li, Timothy Patrick Sheahan · 2010 to 2026
$4.7M
Structure-based design of coronavirus subunit vaccinesR01AI139092 · NIAID · NEW YORK BLOOD CENTER · PI DU, LANYING · 2018 to 2022
$4.2M
Genetic Analysis of COVID-19 Susceptibility and Resistance Determinants in the Collaborative CrossR01AI157253 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BARIC, RALPH S, HEISE, MARK T · 2020 to 2024
$3.8M
Pathogenesis of and host response to chikungunya virus infection of the central nervous systemK01OD026529 · OD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BAXTER, VICTORIA K · 2018 to 2022
$631k
NIAID NIH HHS R01 AI089728NIAID NIH HHS R01 AI110700NIAID NIH HHS R01 AI139092NIAID NIH HHS R01 AI157253NIAID NIH HHS T32 AI007151NIAID NIH HHS T32 AI007419NIAID NIH HHS U01 AI149644NIH HHS K01 OD026529
6 · The paper itself

Abstract

The key to battling the COVID-19 pandemic and its potential aftermath is to develop a variety of vaccines that are efficacious and safe, elicit lasting immunity, and cover a range of SARS-CoV-2 variants. Recombinant viral receptor-binding domains (RBDs) are safe vaccine candidates but often have limited efficacy due to the lack of virus-like immunogen display pattern. Here we have developed a novel virus-like nanoparticle (VLP) vaccine that displays 120 copies of SARS-CoV-2 RBD on its surface. This VLP-RBD vaccine mimics virus-based vaccines in immunogen display, which boosts its efficacy, while maintaining the safety of protein-based subunit vaccines. Compared to the RBD vaccine, the VLP-RBD vaccine induced five times more neutralizing antibodies in mice that efficiently blocked SARS-CoV-2 from attaching to its host receptor and potently neutralized the cell entry of variant SARS-CoV-2 strains, SARS-CoV-1, and SARS-CoV-1-related bat coronavirus. These neutralizing immune responses induced by the VLP-RBD vaccine did not wane during the two-month study period. Furthermore, the VLP-RBD vaccine effectively protected mice from SARS-CoV-2 challenge, dramatically reducing the development of clinical signs and pathological changes in immunized mice. The VLP-RBD vaccine provides one potentially effective solution to controlling the spread of SARS-CoV-2.

Indexed as

Immunogenicity, VaccineAngiotensin-Converting Enzyme 2AnimalsAntibodies, NeutralizingAntibodies, ViralCOVID-19COVID-19 VaccinesDisease Models, AnimalDrug DesignFemaleHEK293 CellsHumansLungMiceMice, Inbred BALB CNanoparticlesAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralCOVID-19 Vaccines

Identifiers

PMID34492082
PMCPMC8448314

What OpenQuestion holds

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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.