# Modeling Human Airway Epithelial Barrier Penetration Using Birch Bet v 1 and Alder Aln g 1 Pollen Allergens During Sensitization Process

**Authors:** Daria N. Melnikova, Andrey E. Potapov, Tatiana V. Ovchinnikova, Ivan V. Bogdanov

PMC · DOI: 10.3390/ijms26115169 · 2025-05-28

## TL;DR

This study compares how two pollen allergens interact with human airway cells, showing how they may trigger allergic reactions.

## Contribution

The study reveals novel insights into how Aln g 1 and Bet v 1 allergens affect epithelial barrier function and immune signaling during sensitization.

## Key findings

- Both Aln g 1 and Bet v 1 allergens disrupt liposomes modeling pulmonary surfactant.
- Aln g 1 and Bet v 1 show similar transport efficiency through an artificial epithelial barrier.
- Aln g 1 upregulates immune-related genes like IL-33, TSLP, IL-1β, and CXCL8 in epithelial cells.

## Abstract

Pollen allergy is rated as a major public health problem, causing significant morbidity and adversely affecting the quality of people’s lives. The airway epithelium serves as the first line of defense in the respiratory system, playing a crucial role in orchestrating immune responses to allergens. In this work, we studied the important transport steps in the major alder pollen allergen Aln g 1 through the human airway epithelium in comparison with those of the birch pollen allergen Bet v 1. Using fluorescence spectroscopy, we showed that both allergens can destroy liposomes with a composition modeling the adult human pulmonary surfactant. Using a polarized Calu-3 monolayer, we showed similar efficiencies of Aln g 1 and Bet v 1 transport through the artificial epithelial barrier. Using qPCR, we showed that Aln g 1 upregulates the expression of IL-33, TSLP, IL-1β, CXCL8 in epithelial cells, playing an important role in the sensitization process. The obtained results may improve our understanding of the primary sensitization mechanisms with the involvement of the PR-10 family of lipid-binding allergens.

## Linked entities

- **Genes:** IL33 (interleukin 33) [NCBI Gene 90865], TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480], IL1B (interleukin 1 beta) [NCBI Gene 3553], CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576]

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL33 (interleukin 33) [NCBI Gene 90865] {aka C9orf26, DVS27, IL1F11, NF-HEV, NFEHEV}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480]
- **Diseases:** Pollen allergy (MESH:D006255)
- **Chemicals:** lipid (MESH:D008055), Aln g 1 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** Calu-3 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0609)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12155471/full.md

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Source: https://tomesphere.com/paper/PMC12155471