Evidence map›Paper›PMID 24736006›Full record

ArticleVaccine2014

Purified coronavirus spike protein nanoparticles induce coronavirus neutralizing antibodies in mice.

Christopher M Coleman, Ye V Liu, Haiyan Mu, Justin K Taylor, Michael Massare, David C Flyer, Gale E Smith, Matthew B Frieman

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 187 papers.

0numbers the graph read from it
0cells of the map it votes in
187citing papers in PubMed
10.1field-weighted citation impact, top 1% 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

187 citing papers in PubMed, 305 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review on Approved and Inprogress COVID-19 Vaccines.Iranian journal of pharmaceutical research : IJPR · 2022
    Review
  20. Review

127 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Christopher M Coleman *University of Maryland School of Medicine 685 West Baltimore St Baltimore, MD 21201.
Ye V Liu *Novavax, Inc. 22 Firstfield Rd Gaithersburg, MD 20852.
Haiyan MuNovavax, Inc. 22 Firstfield Rd Gaithersburg, MD 20852.
Justin K TaylorUniversity of Maryland School of Medicine 685 West Baltimore St Baltimore, MD 21201.
Michael MassareNovavax, Inc. 22 Firstfield Rd Gaithersburg, MD 20852.
David C FlyerNovavax, Inc. 22 Firstfield Rd Gaithersburg, MD 20852.
Gale E Smith *Novavax, Inc. 22 Firstfield Rd Gaithersburg, MD 20852.
Matthew B Frieman *University of Maryland School of Medicine 685 West Baltimore St Baltimore, MD 21201.
Novavax (United States) · USUniversity of Maryland, Baltimore · US

Funding

Role of the Epithelial Growth Factor Receptor in SARS Coronavirus PathogenesisR01AI095569 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI FRIEMAN, MATTHEW BRYAN · 2011 to 2016
$2.3M
NIAID NIH HHS R01 AI095569
6 · The paper itself

Abstract

Development of vaccination strategies for emerging pathogens are particularly challenging because of the sudden nature of their emergence and the long process needed for traditional vaccine development. Therefore, there is a need for development of a rapid method of vaccine development that can respond to emerging pathogens in a short time frame. The emergence of severe acute respiratory syndrome coronavirus (SARS-CoV) in 2003 and Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in late 2012 demonstrate the importance of coronaviruses as emerging pathogens. The spike glycoproteins of coronaviruses reside on the surface of the virion and are responsible for virus entry. The spike glycoprotein is the major immunodominant antigen of coronaviruses and has proven to be an excellent target for vaccine designs that seek to block coronavirus entry and promote antibody targeting of infected cells. Vaccination strategies for coronaviruses have involved live attenuated virus, recombinant viruses, non-replicative virus-like particles expressing coronavirus proteins or DNA plasmids expressing coronavirus genes. None of these strategies has progressed to an approved human coronavirus vaccine in the ten years since SARS-CoV emerged. Here we describe a novel method for generating MERS-CoV and SARS-CoV full-length spike nanoparticles, which in combination with adjuvants are able to produce high titer antibodies in mice.

Indexed as

NanoparticlesAdjuvants, ImmunologicAnimalsAntibodies, NeutralizingAntibodies, ViralCoronavirusCoronavirus InfectionsCross ProtectionMiceMice, Inbred BALB CNeutralization TestsRecombinant ProteinsSpike Glycoprotein, CoronavirusViral VaccinesAdjuvants, ImmunologicAntibodies, NeutralizingAntibodies, ViralRecombinant ProteinsSpike Glycoprotein, CoronavirusViral VaccinesMiddle East Respiratory Syndrome CoronavirusNeutralizing antibodySevere Acute Respiratory Syndrome CoronavirusVaccine

Identifiers

PMID24736006
PMCPMC4058772
OpenAlexW2031436792

What OpenQuestion 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 OpenQuestion graph.