Evidence map›Paper›PMID 42183239›Full record

ArticleFrontiers in immunology2026

A human-on-human assay for detecting anti-myocardial antibodies in patients with myocardial disease.

Anne Auer, Johanna Siegel, Stasa Janjatovic, Margarete Heinrichs, Stefan Störk, Peter Heuschmann, Caroline Morbach, Katrin Streckfuss-Bömeke, Gustavo C Ramos, Katrin G Heinze

Abstract read
In one paragraph

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Anne Auer *Rudolf Virchow Center for Integrative and Translational Bioimaging, Julius-Maximilians-Universität Würzburg (JMU), Würzburg, Germany.
Johanna Siegel *Department of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
Stasa JanjatovicInstitute of Pharmacology and Toxicology, Julius-Maximilians-Universität Würzburg (JMU), Würzburg, Germany.
Margarete HeinrichsDepartment of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
Stefan StörkDepartment of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
Peter HeuschmannInstitute of Clinical Epidemiology and Biometry, Julius-Maximilians-Universität Würzburg (JMU), Würzburg, Germany.
Caroline MorbachDepartment of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
Katrin Streckfuss-BömekeInstitute of Pharmacology and Toxicology, Julius-Maximilians-Universität Würzburg (JMU), Würzburg, Germany.
Gustavo C RamosDepartment of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
Katrin G HeinzeRudolf Virchow Center for Integrative and Translational Bioimaging, Julius-Maximilians-Universität Würzburg (JMU), Würzburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adaptive immune responses, particularly the production of anti-myocardial antibodies, have been implicated as critical mediators in myocardial healing and remodeling following myocardial infarction (MI), acute myocarditis (Myo), and heart failure (HF). However, current methods for detecting heart-reactive antibodies in patients are insufficient, as most rely on heart tissue slices from primates or other species. These approaches pose technical, logistical, and ethical challenges, including the risk of false negative results due to lack of inter-species cross-reactivity. To address these limitations, we developed a human cell-based assay to screen for patient-derived serum or plasma reactivity against human cardiomyocytes differentiated from induced pluripotent stem cells (iPSC-CMs). This human-on-human test system can detect cardiomyocyte-specific immunoglobulins present in patient plasma by applying indirect immunofluorescence staining, followed by convenient visualization through either confocal microscopy or standard widefield systems available in clinical laboratories. Overall, this approach provides a physiologically relevant and ethically responsible model for rapid, accurate testing of anti-myocardial antibodies across various clinical settings, thus offering accessible tools to stratify patients with myocardial disease according to their adaptive immune response status.

Indexed as

AutoantibodiesCardiomyopathiesMyocardiumMyocytes, CardiacHumansInduced Pluripotent Stem CellsMyocardial InfarctionMyocarditisAutoantibodiesantibodiesanti-myocardialhuman iPSC-CMsimmunofluorescencemyocardial infarctionmyocarditis

Identifiers

PMID42183239
PMCPMC13194094

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