Evidence map›Paper›PMID 40880472›Full record

ArticleScience advances2025

STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndrome.

Virginia Andreani, Aaron James Forde, Manfred Fliegauf, Giulia Bressan, Vera Noé, Nils Ott, Shiva Saghafi, Larsen Vornholz, Sophie E Isay, Jürgen Ruland and 2 more

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. How I Treat: STAT3 hyper IgE syndrome.Journal of human immunity · 2026
    Review
  2. Article
  3. Review
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

12 authors.

Virginia AndreaniInstitute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0002-8991-038X
Aaron James FordeInstitute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0003-3754-5541
Manfred FliegaufInstitute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0001-5860-6177
Giulia BressanInstitute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Vera NoéInstitute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Nils OttInstitute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0003-3139-1924
Shiva SaghafiImmunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0001-8546-3247
Larsen VornholzTranslaTUM-Central Institute for Translational Cancer Research, Technical University of Munich, Munich, Germany.ORCID 0000-0002-8054-5603
Sophie E IsayTranslaTUM-Central Institute for Translational Cancer Research, Technical University of Munich, Munich, Germany.ORCID 0000-0002-0495-2944
Jürgen RulandTranslaTUM-Central Institute for Translational Cancer Research, Technical University of Munich, Munich, Germany.ORCID 0000-0002-8381-3597
Philipp HennekeInstitute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0001-7314-7984
Bodo GrimbacherInstitute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0002-6897-6806

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The autosomal dominant hyper-IgE syndrome (AD-HIES) is a primary immunodeficiency, which originates from heterozygous missense mutations in the signal transducer and activator of transcription 3 (

Indexed as

HaploinsufficiencyJob SyndromeSTAT3 Transcription FactorAnimalsDisease Models, AnimalFemaleHeterozygoteHumansImmunoglobulin EMaleMicePedigreeTh17 CellsImmunoglobulin ESTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID40880472
PMCPMC12396324

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.