Evidence map›Paper›PMID 35617962›Full record

ArticleCell reports2022

IgG targeting distinct seasonal coronavirus- conserved SARS-CoV-2 spike subdomains correlates with differential COVID-19 disease outcomes.

Jose L Garrido, Matías A Medina, Felipe Bravo, Sarah McGee, Francisco Fuentes-Villalobos, Mario Calvo, Yazmin Pinos, James W Bowman, Christopher D Bahl, Maria Ines Barria and 2 more

Abstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–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

11 citing papers in PubMed.

  1. Article
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  8. Impact of cross-coronavirus immunity in post-acute sequelae of COVID-19.medRxiv : the preprint server for health sciences · 2022
    Article
  9. Review
  10. Article
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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

12 authors.

Jose L GarridoIchor Biologics LLC, New York, NY 10027, USA; Facultad de Medicina y Ciencia, Universidad San Sebastián, Puerto Montt 5480000, Chile.
Matías A MedinaDepartment of Microbiology, Faculty of Biological Science, Universidad de Concepción, Concepción 4070386, Chile.
Felipe BravoIchor Biologics LLC, New York, NY 10027, USA; Department of Microbiology, Faculty of Biological Science, Universidad de Concepción, Concepción 4070386, Chile.
Sarah McGeeIchor Biologics LLC, New York, NY 10027, USA.
Francisco Fuentes-VillalobosDepartment of Microbiology, Faculty of Biological Science, Universidad de Concepción, Concepción 4070386, Chile.
Mario CalvoInstitute of Medicine, Universidad Austral de Chile, Valdivia 5110566, Chile.
Yazmin PinosHospital Base San José, Osorno 5290000, Chile.
James W BowmanInstitute for Protein Innovation, Harvard Institutes of Medicine, Boston, MA 02115, USA; Division of Hematology/Oncology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; AI Proteins, Andover, MA 01810, USA.
Christopher D BahlInstitute for Protein Innovation, Harvard Institutes of Medicine, Boston, MA 02115, USA; Division of Hematology/Oncology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; AI Proteins, Andover, MA 01810, USA.
Maria Ines BarriaFacultad de Medicina y Ciencia, Universidad San Sebastián, Puerto Montt 5480000, Chile.
Rebecca A BrachmanJacobs Technion-Cornell Institute, Cornell Tech, Cornell University, New York, NY 10044, USA; 525 Bio LLC, New York, NY 10044, USA.
Raymond A AlvarezIchor Biologics LLC, New York, NY 10027, USA; 525 Bio LLC, New York, NY 10044, USA; Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: ralvarez@ichorbiologics.com.

Funding

Development of broadly neutralizing antibodies to treat hantavirus infectionsR43AI138740 · NIAID · ICHOR BIOLOGICS, LLC · PI ALVAREZ, RAYMOND · 2019 to 2020
$355k
NIAID NIH HHS R43 AI138740
6 · The paper itself

Abstract

Despite SARS-CoV-2 being a "novel" virus, early detection of anti-spike IgG in severe COVID-19 patients may be caused by the amplification of humoral memory responses against seasonal coronaviruses. Here, we examine this phenomenon by characterizing anti-spike IgG responses in non-hospitalized convalescent individuals across a spectrum of COVID-19 severity. We observe that disease severity positively correlates with anti-spike IgG levels, IgG cross-reactivity against other betacoronaviruses (β-CoVs), and FcγR activation. Analysis of IgG targeting β-CoV-conserved and non-conserved immunodominant epitopes within the SARS-CoV-2 spike protein revealed epitope-specific relationships: IgG targeting the conserved heptad repeat (HR) 2 region significantly correlates with milder disease, while targeting the conserved S2'FP region correlates with more severe disease. Furthermore, a lower HR2-to-S2'FP IgG-binding ratio correlates with greater disease severity, with ICU-hospitalized COVID-19 patients showing the lowest HR2/S2'FP ratios. These findings suggest that HR2/S2'FP IgG profiles may predict disease severity and offer insight into protective versus deleterious humoral recall responses.

Indexed as

COVID-19SARS-CoV-2HumansImmunoglobulin GSeasonsSpike Glycoprotein, CoronavirusImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2ADEantibody-mediated effector responsesCOVID-19CP: ImmunologyCP: Microbiologydisease severityFc-gamma receptor activationfusion protein regionheptad repeat regionhuman betacoronavirusOC43SARS1SARS-CoV-2

Identifiers

PMID35617962
PMCPMC9108089

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.