Evidence map›Paper›PMID 35355988›Full record

ArticleFrontiers in immunology2022

Heterologous Immune Responses of Serum IgG and Secretory IgA Against the Spike Protein of Endemic Coronaviruses During Severe COVID-19.

Wouter L Smit, Sophie van Tol, Sanne van der Wal, Femke van Vulpen, Shannon la Grouw, Lenneke van Lelyveld, Gijs Limonard, Ailko Bossink, Gert-Jan Godeke, Sandhya Shrestha and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. SIgA in various pulmonary diseases.European journal of medical research · 2023
    Review
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  7. 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

15 authors at 2 institutions in 1 country.

Wouter L SmitDepartment of Medical Microbiology and Immunology, Diakonessenhuis Utrecht, Utrecht, Netherlands.
Sophie van TolCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.
Sanne van der WalDepartment of Medical Microbiology and Immunology, Diakonessenhuis Utrecht, Utrecht, Netherlands.
Femke van VulpenDepartment of Medical Microbiology and Immunology, Diakonessenhuis Utrecht, Utrecht, Netherlands.
Shannon la GrouwDepartment of Medical Microbiology and Immunology, Diakonessenhuis Utrecht, Utrecht, Netherlands.
Lenneke van LelyveldDepartment of Intensive Care, Diakonessenhuis Utrecht, Utrecht, Netherlands.
Gijs LimonardDepartment of Pulmonary Diseases, Diakonessenhuis Utrecht, Utrecht, Netherlands.
Ailko BossinkDepartment of Pulmonary Diseases, Diakonessenhuis Utrecht, Utrecht, Netherlands.
Gert-Jan GodekeCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.
Sandhya ShresthaCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.
Johan ReimerinkCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.
Dirk EgginkCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.
Chantal ReuskenCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.
Michiel HeronDepartment of Medical Microbiology and Immunology, Diakonessenhuis Utrecht, Utrecht, Netherlands.
Steven ThijsenDepartment of Medical Microbiology and Immunology, Diakonessenhuis Utrecht, Utrecht, Netherlands.
Diakonessenhuis hospital · NLNational Institute for Public Health and the Environment · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defining immune correlates of disease severity is important to better understand the immunopathogenesis in COVID-19. Here we made use of a protein microarray platform to detect IgG- and IgA-reactive antibodies in sera and saliva respectively, and assess cross-reactivity between SARS-CoV-2 and endemic coronaviruses (eCoVs). IgG responses against the full protein of spike, but not the S1 subunit, were significantly higher in convalescent sera of patients with severe disease compared to mild disease and healthy controls. In addition, we detected reactivity of secretory IgA to eCoVs in saliva of patients with severe disease, not present in patients with moderate disease or seropositive healthy controls. These heterologous immune responses are in line with non-protective cross-reactivity, and support a potential role for immune imprinting in the pathogenesis of severe COVID-19.

Indexed as

COVID-19Antibodies, ViralCOVID-19 SerotherapyHumansImmunityImmunization, PassiveImmunoglobulin AImmunoglobulin A, SecretoryImmunoglobulin GSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, ViralImmunoglobulin AImmunoglobulin A, SecretoryImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19immune imprintingSARS-CoV-2seasonal coronavirusesspike protein

Identifiers

PMID35355988
PMCPMC8959642
OpenAlexW4220806512

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.