Evidence map›Paper›PMID 40038712›Full record

ArticleVirology journal2025

Frequency of IgE antibody response to SARS-CoV-2 RBD protein across different disease severity COVID19 groups.

Juan Francisco Delgado de la Poza, Albert Rodrigo Parés, Isabel Aparicio-Calvente, Indira Bhambi Blanco, Jordi Gratacòs Masmitjà, Antoni Berenguer-Llergo, Joan Calvet Fontova

Abstract read
In one paragraph

Article in Virology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. 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

7 authors.

Juan Francisco Delgado de la PozaImmunology Laboratory, Clinic Laboratories Service, Departament de Medicina, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain. jdelgado@tauli.cat.
Albert Rodrigo ParésInflammatory Joint Diseases, Bone Metabolism, and Systemic Autoimmune Diseases Research Group, Consorci Corporació Sanitària Parc Taulí, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Sabadell, Spain.
Isabel Aparicio-CalventeImmunology Laboratory, Clinic Laboratories Service, Departament de Medicina, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Indira Bhambi BlancoImmunology Laboratory, Clinic Laboratories Service, Departament de Medicina, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Jordi Gratacòs MasmitjàRheumatology Service, Departament de Medicina, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Antoni Berenguer-LlergoInflammatory Joint Diseases, Bone Metabolism, and Systemic Autoimmune Diseases Research Group, Consorci Corporació Sanitària Parc Taulí, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Sabadell, Spain.
Joan Calvet FontovaRheumatology Service, Departament de Medicina, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCOVID-19 appears to have a progression of three stages. The latter stage is characterized by a high level of cytokine release, which in turn triggers an uncontrolled reaction known as cytokine storm where mast cells are involved. The presence of anti-IgE antibodies against SARS-CoV-2 in this phase has been previously reported, suggesting an association with the severity of the disease. Our study aims to assess the prognostic significance of IgE antibodies against SARS-CoV-2 across a spectrum of clinical presentations, including individual with mild symptoms, hospitalized patients, and those who presented a critical progression.

methodsThe study included 64 patients distributed into the following groups: 22 critically ill hospitalized individuals (Critical); 21 non-critical hospitalized patients (Severe); 21 mild symptomatic non-hospitalized cases (Mild); and 22 healthy blood donors with samples collected in October 2019. Anti-IgE antibodies against Spike (S) protein were detected using a homemade ELISA, where the plate was sensitized with the RBD of recombinant S protein.

resultsAmong 64 SARS-CoV-2 infected patients, 28.1% tested positive for IgE isotype antibodies against S protein RBD, whose prevalence was similar across severity groups: Mild 23.8%, Severe 28.6%, and Critical 31.8% (p = 0.842). Patients with IgE response exhibited higher levels of LDH compared to non-IgE responders, with a 40% increase (p = 0.037), and a non-significantly higher tendency in other inflammatory markers.

conclusionIn SARS-CoV-2 infection, roughly a fourth of patients presented an IgE isotype response, regardless of disease severity, which is associated with higher levels of LDH.

Indexed as

Antibody FormationCOVID-19Immunoglobulin EAdultAgedAged, 80 and overAntibodies, ViralEnzyme-Linked Immunosorbent AssayFemaleHumansMaleMiddle AgedPatient AcuityProtein Interaction Domains and MotifsSpike Glycoprotein, CoronavirusYoung AdultAntibodies, ViralImmunoglobulin ESpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Antibody responseIgEPrognostic factorSARS-CoV-2S protein

Identifiers

PMID40038712
PMCPMC11877796

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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.