Evidence map›Paper›PMID 33123165›Full record

ReviewFrontiers in immunology2020

Progress and Pitfalls in the Quest for Effective SARS-CoV-2 (COVID-19) Vaccines.

Katie L Flanagan, Emma Best, Nigel W Crawford, Michelle Giles, Archana Koirala, Kristine Macartney, Fiona Russell, Benjamin W Teh, Sophie Ch Wen

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 3 pooled it
–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

51 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Efficacy and Safety of BCG Revaccination WithFrontiers in immunology · 2022
    Trial
  5. Article
  6. Antibody-dependent enhancement of coronaviruses.International journal of biological sciences · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Vaccines platforms and COVID-19: what you need to know.Tropical diseases, travel medicine and vaccines · 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

9 authors.

Katie L FlanaganDepartment of Infectious Diseases, Launceston General Hospital, Launceston, TAS, Australia.
Emma BestDepartment of Paediatric Infectious Diseases, Starship Children's Hospital, Auckland, New Zealand.
Nigel W CrawfordDepartment of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.
Michelle GilesDepartment of Obstetrics and Gynaecology, Monash University, Melbourne, VIC, Australia.
Archana KoiralaDepartment of Child and Adolescent Health, University of Sydney, Sydney, NSW, Australia.
Kristine MacartneyDepartment of Child and Adolescent Health, University of Sydney, Sydney, NSW, Australia.
Fiona RussellDepartment of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.
Benjamin W TehDepartment of Infectious Diseases, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Sophie Ch WenInfection Management Prevention Services, Queensland Children's Hospital, South Brisbane, QLD, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are currently around 200 SARS-CoV-2 candidate vaccines in preclinical and clinical trials throughout the world. The various candidates employ a range of vaccine strategies including some novel approaches. Currently, the goal is to prove that they are safe and immunogenic in humans (phase 1/2 studies) with several now advancing into phase 2 and 3 trials to demonstrate efficacy and gather comprehensive data on safety. It is highly likely that many vaccines will be shown to stimulate antibody and T cell responses in healthy individuals and have an acceptable safety profile, but the key will be to confirm that they protect against COVID-19. There is much hope that SARS-CoV-2 vaccines will be rolled out to the entire world to contain the pandemic and avert its most damaging impacts. However, in all likelihood this will initially require a targeted approach toward key vulnerable groups. Collaborative efforts are underway to ensure manufacturing can occur at the unprecedented scale and speed required to immunize billions of people. Ensuring deployment also occurs equitably across the globe will be critical. Careful evaluation and ongoing surveillance for safety will be required to address theoretical concerns regarding immune enhancement seen in previous contexts. Herein, we review the current knowledge about the immune response to this novel virus as it pertains to the design of effective and safe SARS-CoV-2 vaccines and the range of novel and established approaches to vaccine development being taken. We provide details of some of the frontrunner vaccines and discuss potential issues including adverse effects, scale-up and delivery.

Indexed as

AdolescentAdultAgedAged, 80 and overAntibodies, NeutralizingAntibodies, ViralBetacoronavirusCoronavirus InfectionsCOVID-19COVID-19 VaccinesHumansMiddle AgedPandemicsPneumonia, ViralSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Viral Vaccinesadverse events of special interest (AESI)antibody dependent enhancement (ADE)bacillus Calmette-Guérin (BCG)cell mediated immunityCoalition for Epidemic Preparedness Innovations (CEPI)innate immunityneutralizing antibodiesspike protein

Identifiers

PMID33123165
PMCPMC7566192

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.