Evidence map›Paper›PMID 34861490›Full record

ArticleEBioMedicine2021

Relative Ratios of Human Seasonal Coronavirus Antibodies Predict the Efficiency of Cross-Neutralization of SARS-CoV-2 Spike Binding to ACE2.

Yannick Galipeau, Vinayakumar Siragam, Geneviève Laroche, Erika Marion, Matthew Greig, Michaeline McGuinty, Ronald A Booth, Yves Durocher, Miroslava Cuperlovic-Culf, Steffany A L Bennett and 4 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 54 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Autoantibodies targeting angiotensin-converting enzyme 2 are prevalent and not induced by SARS-CoV-2 infection.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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 3 institutions in 1 country.

Yannick GalipeauDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada.
Vinayakumar SiragamDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada.
Geneviève LarocheDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada.
Erika MarionDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada.
Matthew GreigDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada.
Michaeline McGuintyThe Ottawa Hospital Research Institute.
Ronald A BoothUniversity of Ottawa & The Ottawa Hospital Department of Pathology and Laboratory Medicine and The Eastern Ontario Regional Laboratory Association (EORLA).
Yves DurocherHuman Health Therapeutics Research Center, National Research Council Canada.
Miroslava Cuperlovic-CulfDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada; Digital Technologies Research Center, National Research Council Canada; Ottawa Institute of Systems Biology.
Steffany A L BennettDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada; Ottawa Institute of Systems Biology; University of Ottawa Centre for Infection, Immunity and Inflammation (CI3).
Angela M CrawleyDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada; The Ottawa Hospital Research Institute; University of Ottawa Centre for Infection, Immunity and Inflammation (CI3); Department of Biology, Carleton University, Canada.
Patrick M GiguèreDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada.
Curtis CooperThe Ottawa Hospital Research Institute.
Marc-André LangloisDepartment of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada; University of Ottawa Centre for Infection, Immunity and Inflammation (CI3). Electronic address: langlois@uottawa.ca.
University of Ottawa · CAOttawa Hospital · CANational Research Council Canada · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntibodies raised against human seasonal coronaviruses (sCoVs), which are responsible for the common cold, are known to cross-react with SARS-CoV-2 antigens. This prompts questions about their protective role against SARS-CoV-2 infections and COVID-19 severity. However, the relationship between sCoVs exposure and SARS-CoV-2 correlates of protection are not clearly identified.

methodsWe performed a cross-sectional analysis of cross-reactivity and cross-neutralization to SARS-CoV-2 antigens (S-RBD, S-trimer, N) using pre-pandemic sera from four different groups: pediatrics and adolescents, individuals 21 to 70 years of age, older than 70 years of age, and individuals living with HCV or HIV. Data was then further analysed using machine learning to identify predictive patterns of neutralization based on sCoVs serology.

findingsAntibody cross-reactivity to SARS-CoV-2 antigens varied between 1.6% and 15.3% depending on the cohort and the isotype-antigen pair analyzed. We also show a range of neutralizing activity (0-45%) with median inhibition ranging from 17.6 % to 23.3 % in serum that interferes with SARS-CoV-2 spike attachment to ACE2 independently of age group. While the abundance of sCoV antibodies did not directly correlate with neutralization, we show that neutralizing activity is rather dependent on relative ratios of IgGs in sera directed to all four sCoV spike proteins. More specifically, we identified antibodies to NL63 and OC43 as being the most important predictors of neutralization.

interpretationOur data support the concept that exposure to sCoVs triggers antibody responses that influence the efficiency of SARS-CoV-2 spike binding to ACE2, which may potentially impact COVID-19 disease severity through other latent variables.

fundingThis study was supported by a grant by the CIHR (VR2 -172722) and by a grant supplement by the CITF, and by a NRC Collaborative R&D Initiative Grant (PR031-1).

Indexed as

AdolescentAdultAgedAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralCommon ColdCoronavirus 229E, HumanCoronavirus NL63, HumanCoronavirus OC43, HumanCOVID-19Cross ReactionsCross-Sectional StudiesHumansMiddle AgedSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2229ECOVID-19HKU1human coronavirusesNL63OC43pre-existing immunitySARS-CoV-2seasonal coronavirus

Identifiers

PMID34861490
PMCPMC8629681
OpenAlexW3215251263

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.