Evidence map›Paper›PMID 42769530›Full record

ReviewFrontiers in immunology2026

Overlapping type 2, barrier, and remodeling endotypes shape clinical expression in eosinophilic esophagitis.

Adam Wawrzeńczyk, Katarzyna Napiórkowska-Baran, Marta Tykwińska, Maciej Szota, Zbigniew Bartuzi, Józef Sławatycki, Alina Kanikowska, Krzysztof Pałgan

Abstract readReview
In one paragraph

Review 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

8 authors.

Adam WawrzeńczykDepartment of Allergology, Clinical Immunology and Internal Diseases, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, Poland.
Katarzyna Napiórkowska-BaranDepartment of Allergology, Clinical Immunology and Internal Diseases, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, Poland.
Marta TykwińskaDepartment of Allergology, Clinical Immunology and Internal Diseases, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, Poland.
Maciej SzotaDepartment of Allergology, Clinical Immunology and Internal Diseases, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, Poland.
Zbigniew BartuziDepartment of Allergology, Clinical Immunology and Internal Diseases, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, Poland.
Józef SławatyckiStudent Research Club of Clinical Immunology, Department of Allergology, Clinical Immunology and Internal Diseases, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, Poland.
Alina KanikowskaDepartment of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Poznan, Poland.
Krzysztof PałganDepartment of Allergology, Clinical Immunology and Internal Diseases, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eosinophilic esophagitis (EoE) is a chronic, immune-mediated disease of the esophagus in which symptoms, histologic activity, endoscopic severity, epithelial dysfunction, and fibrostenotic remodeling frequently diverge. Peak eosinophil density remains central to diagnosis and response assessment, but it represents only one component of a broader epithelial-immune and structural process. This review integrates epithelial alarmins, local type 2 immunity, IL-13-driven epithelial programming, eosinophil-mast-cell effector activity, and stromal remodeling within an endotype-to-phenotype framework. We propose that inflammatory, barrier-dominant, relapsing, treatment-responsive, fibrostenotic, and mixed clinical patterns reflect overlapping programs rather than discrete diseases. The strength of evidence differs across the framework: IL-13-associated epithelial activity, eosinophil-mast-cell injury, and remodeling pathways are supported by human tissue, treatment, and functional studies, whereas alarmin-dominant, barrier-relapse, and biomarker-matched treatment constructs remain largely mechanistic or hypothesis-generating. Eosinophils remain biologically active effector cells, but their number alone does not capture degranulation, mast-cell activity, epithelial repair, or accumulated structural injury. We therefore distinguish symptomatic, histologic, endoscopic, molecular, and structural or functional remission and emphasize the complementary roles of EREFS, broader histologic scoring, and structural assessment. The proposed model is a conceptual synthesis of published evidence, not a validated routine treatment-selection algorithm, but it may support future longitudinal validation and stratified research.

Indexed as

Eosinophilic EsophagitisEosinophilsAnimalsEsophagusHumansInterleukin-13Mast CellsPhenotypeInterleukin-13clinical phenotypeseosinophilic esophagitisepithelial barrierfibrostenosisIL-13molecular endotypesprecision medicinetype 2 immunity

Identifiers

PMID42769530
PMCPMC13591616

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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.