Evidence map›Paper›PMID 34652831›Full record

ArticleAllergy2022

Receptor binding domain-IgG levels correlate with protection in residents facing SARS-CoV-2 B.1.1.7 outbreaks.

Hubert Blain, Edouard Tuaillon, Lucie Gamon, Amandine Pisoni, Stéphanie Miot, Valentin Delpui, Nejm Si-Mohamed, Clémence Niel, Yves Rolland, Brigitte Montes and 7 more

Abstract read
In one paragraph

Article in Allergy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Variant-Specific IgA Protects Against Omicron Infection.The Journal of infectious diseases · 2024
    Trial
  2. Article
  3. Article
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  6. Managing the Impact of COVID-19 in Nursing Homes and Long-Term Care Facilities: An Update.Journal of the American Medical Directors Association · 2022
    Article
  7. Article
  8. Observational
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  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

17 authors.

Hubert BlainDepartment of Internal Medicine and Geriatrics, MUSE University, Montpellier, France.
Edouard TuaillonPathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, EFS, Antilles University, University Hospital, Montpellier, France.
Lucie GamonClinical Research and Epidemiology Unit, University Hospital, Montpellier, France.
Amandine PisoniPathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, EFS, Antilles University, University Hospital, Montpellier, France.
Stéphanie MiotDepartment of Internal Medicine and Geriatrics, MUSE University, Montpellier, France.
Valentin DelpuiDepartment of Internal Medicine and Geriatrics, MUSE University, Montpellier, France.
Nejm Si-MohamedDepartment of Internal Medicine and Geriatrics, MUSE University, Montpellier, France.
Clémence NielPathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, EFS, Antilles University, University Hospital, Montpellier, France.
Yves RollandGérontopôle de Toulouse, INSERM 1027, Toulouse, France.
Brigitte MontesPathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, EFS, Antilles University, University Hospital, Montpellier, France.ORCID 0000-0003-2866-4274
Soraya GrocPathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, EFS, Antilles University, University Hospital, Montpellier, France.
Sophia RafasseCEMIPAI, University of Montpellier, UAR3725, CNRS, Montpellier, France.
Anne-Marie DupuyBiochemistry and Hormonology Laboratory, University Hospital, Montpellier, France.
Nathalie GrosCEMIPAI, University of Montpellier, UAR3725, CNRS, Montpellier, France.
Delphine MuriauxCEMIPAI, University of Montpellier, UAR3725, CNRS, Montpellier, France.
Marie-Christine PicotClinical Research and Epidemiology Unit, University Hospital, Montpellier, France.
Jean BousquetDepartment of Dermatology and Allergy, Universitätsmedizin, Berlin, Germany.ORCID 0000-0002-4061-4766

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLimited information exists on nursing home (NH) residents regarding BNT162b2 vaccine efficacy in preventing SARS-CoV-2 and severe COVID-19, and its association with post-vaccine humoral response.

methods396 residents from seven NHs suffering a SARS-CoV-2 B.1.1.7 (VOC-α) outbreak at least 14 days after a vaccine campaign were repeatedly tested using SARS-CoV-2 real-time reverse-transcriptase polymerase chain reaction on nasopharyngeal swab test (RT-qPCR). SARS-CoV-2 receptor-binding domain (RBD) of the S1 subunit (RBD-IgG) was measured in all residents. Nucleocapsid antigenemia (N-Ag) was measured in RT-qPCR-positive residents and serum neutralizing antibodies in vaccinated residents from one NH.

resultsThe incidence of positive RT-qPCR was lower in residents vaccinated by two doses (72/317; 22.7%) vs one dose (10/31; 32.3%) or non-vaccinated residents (21/48; 43.7%; p < .01). COVID-19-induced deaths were observed in 5 of the 48 non-vaccinated residents (10.4%), in 2 of the 31 who had received one dose (6.4%), and in 3 of the 317 (0.9%) who had received two doses (p = .0007). Severe symptoms were more common in infected non-vaccinated residents (10/21; 47.6%) than in infected vaccinated residents (15/72; 21.0%; p = .002). Higher levels of RBD-IgG (n = 325) were associated with a lower SARS-CoV-2 incidence. No in vitro serum neutralization activity was found for RBD-IgG levels below 1050 AU/ml. RBD-IgG levels were inversely associated with N-Ag levels, found as a risk factor of severe COVID-19.

conclusionsTwo BNT162b2 doses are associated with a 48% reduction of SARS-CoV-2 incidence and a 91.3% reduction of death risk in residents from NHs facing a VOC-α outbreak. Post-vaccine RBD-IgG levels correlate with BNT162b2 protection against SARS-CoV-2 B.1.1.7.

Indexed as

COVID-19VaccinesAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesDisease OutbreaksHumansImmunoglobulin GSARS-CoV-2Antibodies, ViralBNT162 VaccineCOVID-19 VaccinesImmunoglobulin GVaccinesantibody responseBNT162b2 vaccineCOVID-19efficacyneutralizing antibodiesnucleocapsid antigenemianursing homesresidentsSARS-CoV-2symptoms

Identifiers

PMID34652831
PMCPMC8652754

What OpenQuestion holds

Textmetadata
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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.