# Food Allergen Component Sensitization Patterns in Eosinophilic Esophagitis: Insights from a Retrospective Comparative Study

**Authors:** Adam Wawrzeńczyk, Katarzyna Napiórkowska-Baran, Kinga Lis, Marta Tykwińska, Maciej Szota, Paweł Treichel, Justyna Durślewicz, Zbigniew Bartuzi

PMC · DOI: 10.3390/foods15040748 · 2026-02-18

## TL;DR

This study compares food allergen sensitization patterns in patients with eosinophilic esophagitis and chronic urticaria, revealing distinct molecular IgE profiles that may reflect dietary exposure rather than immediate allergic reactions.

## Contribution

The study identifies unique sensitization patterns to structurally stable food allergen components in EoE patients, not seen in controls, suggesting these may reflect chronic dietary exposure.

## Key findings

- Sensitization to PR-10 proteins was more common in EoE patients compared to chronic urticaria controls.
- EoE patients showed sensitization to lipid transfer proteins and plant storage proteins, which were absent in controls.
- Component-resolved diagnostics provided descriptive insights but were not useful for directly identifying trigger foods in EoE.

## Abstract

Eosinophilic esophagitis (EoE) is a chronic, food-driven inflammatory disorder of the esophagus in which repeated exposure to dietary antigens plays a central role, yet identification of clinically relevant food triggers remains largely empirical. In this retrospective, single-center study, molecular IgE sensitization profiles were descriptively characterized in adult patients with EoE (n = 22) and compared with an allergic control group with chronic urticaria (CU; n = 29) using component-resolved diagnostics. IgE sensitization was common in both cohorts and predominantly reflected inhalant-related, cross-reactive components, particularly PR-10 proteins (63.6% in EoE vs. 37.9% in CU). In contrast, sensitization to structurally stable food allergen components, including lipid transfer proteins and plant storage proteins, was observed in a subset of patients with EoE (31.8%) and was not detected in the control group (0%; p = 0.0015). These food-derived components are characterized by resistance to thermal processing and gastrointestinal digestion and may reflect patterns of sustained dietary exposure rather than acute IgE-mediated reactions. Consistent with previous observations, component-resolved diagnostics showed limited utility for the direct identification of trigger foods in eosinophilic esophagitis. Accordingly, the observed molecular sensitization patterns should be interpreted as descriptive and hypothesis-generating signals rather than as indicators of pathogenic mechanisms or clinical decision-making tools. The findings highlight the importance of considering molecular properties of food allergen components when interpreting sensitization profiles in chronic, non-IgE-mediated inflammatory diseases and underscore the need for prospective studies integrating standardized clinical and dietary outcomes.

## Linked entities

- **Diseases:** Eosinophilic esophagitis (MONDO:0005361), chronic urticaria (MONDO:0850230)

## Full-text entities

- **Genes:** PVALB (parvalbumin) [NCBI Gene 5816] {aka D22S749}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}
- **Diseases:** Food-Driven Diseases (MESH:D005517), CRD (MESH:C566443), Esophagitis (MESH:D004941), anaphylaxis (MESH:D000707), urticaria (MESH:D014581), atopic disease (MESH:D006969), atopy (MESH:C564133), CU (MESH:D000080223), chest pain (MESH:D002637), Eosinophilia (MESH:D004802), asthma (MESH:D001249), abdominal pain (MESH:D015746), atopic (MESH:C566404), EoE (MESH:D057765), eosinophilic gastrointestinal inflammation (MESH:D007249), mucosal disease (MESH:D004194), injury to (MESH:D014947), Atopic dermatitis (MESH:D003876), inflammatory disorder of the esophagus (MESH:D004938), chronic (MESH:D002908), nausea or vomiting (MESH:D020250), Allergic (MESH:D004342), heartburn (MESH:D006356), Allergic rhinitis (MESH:D065631), esophageal dysfunction (MESH:D004935), oral allergy (MESH:D006967), food allergy (MESH:D005512), weight loss (MESH:D015431), Dysphagia (MESH:D003680), Angioedema (MESH:D000799)
- **Chemicals:** Lipid (MESH:D008055), amino acid (MESH:D000596), carbohydrate (MESH:D002241), CRD (-), disulfide (MESH:D004220)
- **Species:** Actinopterygii (fishes, superclass) [taxon 7898], Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939598/full.md

---
Source: https://tomesphere.com/paper/PMC12939598