Evidence map›Paper›PMID 33785745›Full record

ArticleNPJ vaccines2021

Replicating bacterium-vectored vaccine expressing SARS-CoV-2 Membrane and Nucleocapsid proteins protects against severe COVID-19-like disease in hamsters.

Qingmei Jia, Helle Bielefeldt-Ohmann, Rachel M Maison, Saša Masleša-Galić, Sarah K Cooper, Richard A Bowen, Marcus A Horwitz

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  4. Article
  5. rLVS ΔHuman vaccines & immunotherapeutics · 2025
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  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. LVS ΔmBio · 2024
    Article
  15. Article
  16. Article
  17. Review
  18. Molecular characterization of SARS-CoV-2 nucleocapsid protein.Frontiers in cellular and infection microbiology · 2024
    Review
  19. The rLVS ΔHuman vaccines & immunotherapeutics · 2023
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Qingmei JiaDivision of Infectious Diseases, Department of Medicine, 37-121 Center for Health Sciences, School of Medicine, University of California - Los Angeles, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-2328-4806
Helle Bielefeldt-OhmannSchool of Veterinary Science, University of Queensland, Brisbane, QLD, Australia.ORCID http://orcid.org/0000-0002-5332-5445
Rachel M MaisonDepartment of Biomedical Sciences, Colorado State University, Fort Collins, CO, USA.ORCID http://orcid.org/0000-0002-4003-2643
Saša Masleša-GalićDivision of Infectious Diseases, Department of Medicine, 37-121 Center for Health Sciences, School of Medicine, University of California - Los Angeles, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-8200-6670
Sarah K CooperDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO, USA.ORCID http://orcid.org/0000-0001-9656-2283
Richard A BowenDepartment of Biomedical Sciences, Colorado State University, Fort Collins, CO, USA.
Marcus A HorwitzDivision of Infectious Diseases, Department of Medicine, 37-121 Center for Health Sciences, School of Medicine, University of California - Los Angeles, Los Angeles, CA, USA. MHorwitz@mednet.ucla.edu.ORCID http://orcid.org/0000-0001-6525-7147
Colorado State University · USUniversity of California, Los Angeles · USThe University of Queensland · AU

Funding

Development of a Safe and Potent Vaccine Against Melioidosis using the LVS dcapB Vector PlatformR01AI141390 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HORWITZ, MARCUS AARON · 2019 to 2023
$3.9M
CSU Infectious Disease Research and Response Training ProgramT32AI162691 · NIAID · COLORADO STATE UNIVERSITY · PI DEAN, GREGG A · 2021 to 2025
$2.1M
NIAID NIH HHS R01 AI141390NIAID NIH HHS T32 AI162691U.S. Department of Health & Human Services | National Institutes of Health (NIH) AI141390
6 · The paper itself

Abstract

To generate an inexpensive readily manufactured COVID-19 vaccine, we employed the LVS ΔcapB vector platform, previously used to generate potent candidate vaccines against Select Agent diseases tularemia, anthrax, plague, and melioidosis. Vaccines expressing SARS-CoV-2 structural proteins are constructed using the LVS ΔcapB vector, a highly attenuated replicating intracellular bacterium, and evaluated for efficacy in golden Syrian hamsters, which develop severe COVID-19-like disease. Hamsters immunized intradermally or intranasally with a vaccine co-expressing the Membrane and Nucleocapsid proteins and challenged 5 weeks later with a high dose of SARS-CoV-2 are protected against severe weight loss and lung pathology and show reduced viral loads in the oropharynx and lungs. Protection correlates with anti-Nucleocapsid antibody. This potent vaccine should be safe; inexpensive; easily manufactured, stored, and distributed; and given the high homology between Membrane and Nucleocapsid proteins of SARS-CoV and SARS-CoV-2, potentially serve as a universal vaccine against the SARS subset of pandemic causing β-coronaviruses.

Identifiers

PMID33785745
PMCPMC8009914
OpenAlexW3146939752

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.