Evidence map›Paper›PMID 35289271›Full record

ArticleeLife2022

Boosting of cross-reactive antibodies to endemic coronaviruses by SARS-CoV-2 infection but not vaccination with stabilized spike.

Andrew R Crowley, Harini Natarajan, Andrew P Hederman, Carly A Bobak, Joshua A Weiner, Wendy Wieland-Alter, Jiwon Lee, Evan M Bloch, Aaron A R Tobian, Andrew D Redd and 7 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. 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
4.9field-weighted citation impact, top 4% 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, 50 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 3 countries.

Andrew R Crowley *Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Dartmouth College, Hanover, United States.
Harini Natarajan *Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Dartmouth College, Hanover, United States.
Andrew P HedermanThayer School of Engineering, Dartmouth College, Hanover, United States.
Carly A BobakBiomedical Data Science, Dartmouth College, Hanover, United States.
Joshua A WeinerThayer School of Engineering, Dartmouth College, Hanover, United States.
Wendy Wieland-AlterDepartment of Pediatrics, Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center, Lebanon, United States.
Jiwon LeeThayer School of Engineering, Dartmouth College, Hanover, United States.
Evan M BlochDepartment of Pathology, Johns Hopkins School of Medicine, Baltimore, United States.
Aaron A R TobianDepartment of Pathology, Johns Hopkins School of Medicine, Baltimore, United States.
Andrew D ReddDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, United States.
Joel N BlanksonDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, United States.
Dana WolfHadassah University Medical Center, Jerusalem, Israel.
Tessa GoetghebuerInstitute for Medical Immunology, Université libre de Bruxelles, Charleroi, Belgium.
Arnaud MarchantInstitute for Medical Immunology, Université libre de Bruxelles, Charleroi, Belgium.
Ruth I ConnorDepartment of Pediatrics, Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center, Lebanon, United States.
Peter F WrightDepartment of Pediatrics, Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center, Lebanon, United States.
Margaret E AckermanDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Dartmouth College, Hanover, United States.ORCID 0000-0002-4253-3476
Dartmouth College · USDartmouth–Hitchcock Medical Center · USUniversité Libre de Bruxelles · BEHadassah Medical Center · ILJohns Hopkins University · USNational Institutes of Health · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Fred W Kolling IV · 1985 to 2026
$91.3M
Understanding the role of RNA-binding protein mutations in cancerP20GM113132 · NIGMS · DARTMOUTH COLLEGE · PI MADDEN, DEAN R · 2016 to 2025
$25.9M
Transferred ImmunityU19AI145825 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI PASETTI, MARCELA F · 2021 to 2025
$16.0M
Unlocking the Potential of HIV-Infected Deceased Donors for Organ TransplantationR01AI120938 · NIAID · JOHNS HOPKINS UNIVERSITY · PI TOBIAN, AARON A · 2016 to 2021
$4.3M
Penile Microbiome, Inflammation and HIV Susceptibility During Sexual Debut and Maturation Among Male AdolescentsR01AI128779 · NIAID · JOHNS HOPKINS UNIVERSITY · PI TOBIAN, AARON A · 2017 to 2020
$2.1M
The Malaria Transfusion Risk (MATRix) StudyK23HL151826 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BLOCH, EVAN MARTIN · 2020 to 2024
$882k
NCI NIH HHS P30 CA023108NHLBI NIH HHS K23 HL151826NIAID NIH HHS HHSN272201400008CNIAID NIH HHS R01 AI120938NIAID NIH HHS R01 AI128779NIAID NIH HHS U19 AI145825NIGMS NIH HHS P20 GM113132NIH HHS intramuralNIH HHS K23HL151826NIH HHS P20-GM113132NIH HHS R01AI120938NIH HHS R01 AI120938S1NIH HHS R01AI120938S1NIH HHS R01AI128779NIH HHS U19AI145825
6 · The paper itself

Abstract

Preexisting antibodies to endemic coronaviruses (CoV) that cross-react with SARS-CoV-2 have the potential to influence the antibody response to COVID-19 vaccination and infection for better or worse. In this observational study of mucosal and systemic humoral immunity in acutely infected, convalescent, and vaccinated subjects, we tested for cross-reactivity against endemic CoV spike (S) protein at subdomain resolution. Elevated responses, particularly to the β-CoV OC43, were observed in all natural infection cohorts tested and were correlated with the response to SARS-CoV-2. The kinetics of this response and isotypes involved suggest that infection boosts preexisting antibody lineages raised against prior endemic CoV exposure that cross-react. While further research is needed to discern whether this recalled response is desirable or detrimental, the boosted antibodies principally targeted the better-conserved S2 subdomain of the viral spike and were not associated with neutralization activity. In contrast, vaccination with a stabilized spike mRNA vaccine did not robustly boost cross-reactive antibodies, suggesting differing antigenicity and immunogenicity. In sum, this study provides evidence that antibodies targeting endemic CoV are robustly boosted in response to SARS-CoV-2 infection but not to vaccination with stabilized S, and that depending on conformation or other factors, the S2 subdomain of the spike protein triggers a rapidly recalled, IgG-dominated response that lacks neutralization activity.

Indexed as

Antibodies, ViralAntibody SpecificityCOVID-19COVID-19 VaccinesCross ReactionsHost-Pathogen InteractionsHumansImmunoglobulin AImmunoglobulin GImmunoglobulin MNeutralization TestsSARS-CoV-2Spike Glycoprotein, CoronavirusVaccinationAntibodies, ViralCOVID-19 VaccinesImmunoglobulin AImmunoglobulin GImmunoglobulin MSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2antibodiesconformationepitopehumanimmunologyinfectious diseaseinflammationmicrobiologyneutralizationSARS-CoV-2vaccine

Identifiers

PMID35289271
PMCPMC8923670
OpenAlexW4220820680

What OpenQuestion holds

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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.