Evidence map›Paper›PMID 40165950›Full record

ArticleFrontiers in immunology2025

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

Mario Framil, Lydia García-Serrano, Francisco Morandeira, Juan Francisco Luchoro, Arnau Antolí, Jose Luis Gomez-Vazquez, Àngels Sierra-Fortuny, Xavier Solanich

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
  4. Article
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

8 authors.

Mario FramilImmunology Department, Centre Diagnòstic Biomèdic, Hospital Clínic de Barcelona, Barcelona, Spain.
Lydia García-SerranoImmunology Department, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Spain.
Francisco MorandeiraImmunology Department, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Spain.
Juan Francisco LuchoroImmunology Department, Centre Diagnòstic Biomèdic, Hospital Clínic de Barcelona, Barcelona, Spain.
Arnau AntolíBellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Spain.
Jose Luis Gomez-VazquezBellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Spain.
Àngels Sierra-FortunyBellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Spain.
Xavier SolanichBellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AutoantibodiesCOVID-19Interferon Type ISARS-CoV-2ThrombosisAgedAntibodies, NeutralizingFemaleHumansMaleMiddle AgedRisk FactorsAntibodies, NeutralizingAutoantibodiesInterferon Type ICOVID-19endothelial dysfunctionICU patientsnon-neutralizing autoantibodiesthrombotic complicationstype I interferon

Identifiers

PMID40165950
PMCPMC11955489

What OpenQuestion holds

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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.