Non-neutralizing anti-type I interferon autoantibodies could increase thrombotic risk in critical COVID-19 patients

Bibliographic Details
Title: Non-neutralizing anti-type I interferon autoantibodies could increase thrombotic risk in critical COVID-19 patients
Authors: Mario Framil, Lydia García-Serrano, Francisco Morandeira, Juan Francisco Luchoro, Arnau Antolí, Jose Luis Gomez-Vazquez, Àngels Sierra-Fortuny, Xavier Solanich
Source: Frontiers in Immunology, Vol 16 (2025)
Publisher Information: Frontiers Media S.A., 2025.
Publication Year: 2025
Collection: LCC:Immunologic diseases. Allergy
Subject Terms: non-neutralizing autoantibodies, type I interferon, COVID-19, thrombotic complications, endothelial dysfunction, ICU patients, Immunologic diseases. Allergy, RC581-607
More Details: During the COVID-19 pandemic, approximately 15% of patients with severe COVID-19 pneumonia were reported to have neutralizing anti-type I interferon (IFN) autoantibodies, which impaired the antiviral response and led to a poorer prognosis. However, the physiological impact of non-neutralizing autoantibodies remains unclear. In our cohort of COVID-19 patients admitted to intensive care, the presence of non-neutralizing anti-type I IFN autoantibodies increased the risk of thrombotic complications, likely via a cytokine carrier mechanism, prolonging the half-life of cytokines and dysregulating vascular endothelial function. Previous studies have associated non-neutralizing anti-type I IFN autoantibodies with an increased risk of cardiovascular complications in autoimmune diseases like systemic lupus erythematosus, but their relevance in infectious diseases remains uncertain. Stratifying anti-type I IFN autoantibodies based on their neutralizing capacity may have clinical significance not only in terms of susceptibility to infectious diseases but also in predicting cardiovascular and thrombotic events.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1664-3224
Relation: https://www.frontiersin.org/articles/10.3389/fimmu.2025.1556731/full; https://doaj.org/toc/1664-3224
DOI: 10.3389/fimmu.2025.1556731
Access URL: https://doaj.org/article/e829327374e8487e994b862b1bfdf17a
Accession Number: edsdoj.829327374e8487e994b862b1bfdf17a
Database: Directory of Open Access Journals
More Details
ISSN:16643224
DOI:10.3389/fimmu.2025.1556731
Published in:Frontiers in Immunology
Language:English