# Immune and epithelial responses to textile dyes: the role of chemical structure in toxicity

**Authors:** Lizette M. Cortes

PMC · DOI: 10.3389/falgy.2025.1636419 · 2026-01-09

## TL;DR

This study examines how different textile dyes affect immune and epithelial cells, finding that dye toxicity and inflammation depend on their chemical structure.

## Contribution

The study links specific chemical structures of dyes to their immunotoxic and epithelial effects, offering new insights into dye-induced toxicity mechanisms.

## Key findings

- Disperse Blue 124 increased pro-inflammatory cytokines without cytotoxicity, indicating high sensitization potential.
- Disperse Blue 1 caused high cytotoxicity despite moderate cytokine production, suggesting direct cell damage.
- Nanostring analysis showed epithelial inflammation and barrier disruption with Blue 1 and 124, but not with Blue 79.1 and 183.

## Abstract

Continuous exposure to textile dyes can result in potential health risks, such as inflammatory and allergic responses. We investigated immunotoxicity, and epithelial responses induced by Disperse Blue 1, 124, 79.1, and 183 when in co-culture with swine peripheral blood mononuclear cells (PBMCs), intestinal porcine epithelial cells (IPEC), and human epidermal skin scaffolds. PBMC cytokine production (IFN-γ and TNF-α), cell viability, IPEC gene expression profiles (by Nanostring analysis) and histopathology of human epidermis were evaluated. Disperse Blue 124 strongly increased pro-inflammatory cytokines without significant cytotoxicity, suggesting high sensitization potential. Contrarily, Disperse Blue 1 exhibited high cytotoxicity despite moderate cytokine production. Nanostring analysis revealed prominent epithelial inflammation (CCL20 upregulation) and compromised barrier integrity (CLDN-4) with Blue 1 and Blue 124, but not Blue 79.1 and 183. Histopathology further confirmed epidermal damage, with Blue 1 and 124. Therefore, dye-induced effects correlated with chemical structure, molecular weight, hydrophobicity, and functional groups, supporting the hypothesis that structural properties influence toxicity and absorption.

## Linked entities

- **Genes:** IFNG (interferon gamma) [NCBI Gene 3458], TNF (tumor necrosis factor) [NCBI Gene 7124], CCL20 (C-C motif chemokine ligand 20) [NCBI Gene 6364], CLDN4 (claudin 4) [NCBI Gene 1364]
- **Chemicals:** Disperse Blue 1 (PubChem CID 17190), Disperse Blue 124 (PubChem CID 84802), Disperse Blue 79.1 (PubChem CID 77172), Disperse Blue 183 (PubChem CID 75325)
- **Species:** Mus musculus (taxon 10090), Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CLDN4 (claudin 4) [NCBI Gene 1364] {aka CPE-R, CPER, CPETR, CPETR1, WBSCR8, hCPE-R}, CCL20 (C-C motif chemokine ligand 20) [NCBI Gene 6364] {aka CKb4, Exodus, LARC, MIP-3-alpha, MIP-3a, MIP3A}
- **Diseases:** inflammation (MESH:D007249), allergic responses (MESH:D004342), cytotoxicity (MESH:D064420)
- **Chemicals:** Disperse Blue 1 (MESH:C048853), Blue 124 (-), Disperse Blue 124 (MESH:C069319)
- **Species:** Homo sapiens (human, species) [taxon 9606], Sus scrofa (pig, species) [taxon 9823]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12827529/full.md

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Source: https://tomesphere.com/paper/PMC12827529