Evidence map›Paper›PMID 42021980›Full record

ArticleThe World Allergy Organization journal2026

Autoallergy in chronic rhinosinusitis and its clinical relevance.

Jorge Sánchez, Andres Sánchez, Julian Arango, Dalgys Martinez, Leonardo Puerta

Abstract read
In one paragraph

Article in The World Allergy Organization journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jorge SánchezGroup of Clinical and Experimental Allergy, Hospital "Alma Mater de Antioquia", University of Antioquia, Medellín, Colombia.
Andres SánchezGroup of Clinical and Experimental Allergy, Hospital "Alma Mater de Antioquia", University of Antioquia, Medellín, Colombia.
Julian ArangoGroup of Clinical and Experimental Allergy, Hospital "Alma Mater de Antioquia", University of Antioquia, Medellín, Colombia.
Dalgys MartinezInstitute for Immunological Research, University of Cartagena, Cartagena, Colombia.
Leonardo PuertaInstitute for Immunological Research, University of Cartagena, Cartagena, Colombia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The presence of IgE autoantibodies against human proteins ("autoallergy") has been identified in different type 2 inflammation. Objective: The aim of this study was to evaluate the presence of autoallergy in chronic rhinosinusitis (CRS) and explore its clinical impact. Methods: Cross-sectional study with CRS patients and healthy controls. Three steps were followed: 1) IgE autoantibodies against Fatty Acid Binding Protein (FABP), FABP3 and FABP4, Eosinophil Peroxidase (EPX), and Eosinophil Cationic Protein (ECP) were measured. 2) The allergenic activity of these IgE autoantibodies was evaluated with basophil activation test (BAT) and skin prick test (SPT). 3) Association of these autoantibodies with some clinical outcomes was explored. Results: 22.3% in the CRS group and 12.1% in the control group had at least 1 IgE autoantibody (IgE-AA). In CRS and control group, the most frequent IgE-AA were against EPX (15.9% versus 5.4% Conclusion: IgE autoantibodies are presented in CRS patients and are associated with severe clinical outcomes. Accordingly, autoallergy could be an endophenotype in CRS with clinical relevance as a biomarker of disease activity. Further studies with larger cohorts are warranted to validate these findings.

Indexed as

AllergyAutoimmuneEosinophilsImmunoglobulin ERhinosinusitis

Identifiers

PMID42021980
PMCPMC13098401

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