Evidence map›Paper›PMID 39940781›Full record

ArticleInternational journal of molecular sciences2025

Development of Cell-Assembled Human Endomysial-Type Biomatrix Substrate for the Detection of Celiac Disease Autoantibodies.

Ilma R Korponay-Szabó, Róbert Király, Judit Gyimesi, Markku Mäki

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

4 authors.

Ilma R Korponay-SzabóDepartment of Pediatrics, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0003-0554-2629
Róbert KirályDepartment of Biochemistry and Molecular Biology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0002-1606-3132
Judit GyimesiCeliac Disease Center, Heim Pál National Pediatric Institute, 1089 Budapest, Hungary.
Markku MäkiFaculty of Medicine and Health Technology, Tampere University, 33520 Tampere, Finland.

Funding

European Union Interreg Danube Transnational Programme DTP571 CD SKILLS
6 · The paper itself

Abstract

The endomysial antibody (EMA) immunofluorescent test is a highly specific method to detect disease-specific autoantibodies in celiac disease (CD) by their binding to natural transglutaminase-2 autoantigen in tissue sections, and it is used as a compulsory confirmatory test in the non-invasive diagnosis of CD. The classical EMA substrates are the monkey esophagus and the human umbilical cord. It is increasingly difficult to use these tissues due to ethical concerns and animal welfare regulations. In this study, we developed, in cell culture, an endomysium-type extracellular biomatrix assembled by human umbilical cord vein-derived endothelial cells which binds CD antibodies in a similar pattern as monkey esophagus and has similar macromolecular composition. Evaluating retrospectively and prospectively tested patient cohorts, including 130 CD cases and 105 non-celiac controls, IgA-class celiac antibody detection on the biomatrix was equally specific (100%) as EMA testing on tissues, and had higher sensitivity (95.6% versus 91.2%). Both EMA tests were less sensitive, but more specific than transglutaminase-based ELISA measurements. The decellularization of the biomatrix improved sensitivity, enabled the detection of IgG-class celiac antibodies, and allowed for simple reading without previous training. This easily available cell-assembled biomatrix substrate may replace substrate tissues in diagnostic EMA testing in the future.

Indexed as

AutoantibodiesCeliac DiseaseExtracellular MatrixAdultAgedAnimalsAutoantigensFemaleGTP-Binding ProteinsHumansHuman Umbilical Vein Endothelial CellsImmunoglobulin AImmunoglobulin GMaleMiddle AgedProtein Glutamine gamma Glutamyltransferase 2AutoantibodiesAutoantigensGTP-Binding ProteinsImmunoglobulin AImmunoglobulin GProtein Glutamine gamma Glutamyltransferase 2Transglutaminasesceliac diseasediagnostic accuracyendomysial antibodiesmonkey esophagustransglutaminase antibodies

Identifiers

PMID39940781
PMCPMC11817494

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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.