# A laboratory test to detect gliadin-specific CD4+ T-cells for difficult to diagnose celiac disease

**Authors:** Daan A.R. Castelijn, Nicolette J. Wierdsma, Kim de Buck, Maaike A. van Bree, Tracy-Jane T.H.D. Eisden, Jolien C. Hollander, Gerd Bouma, Hetty J. Bontkes

PMC · DOI: 10.1016/j.jtauto.2025.100301 · 2025-07-24

## TL;DR

A new lab test detects gluten-sensitive T-cells in blood to help diagnose celiac disease in difficult cases.

## Contribution

A simplified flow cytometry method using dextramers to detect gliadin-specific CD4+ T-cells in peripheral blood.

## Key findings

- Gliadin-specific T-cell frequencies were significantly higher in celiac patients compared to controls (p < 0.0001).
- A low-dose gluten challenge increased detectable T-cells in patients on a gluten-free diet.
- The test successfully aided in diagnosing challenging cases like seronegative celiac disease.

## Abstract

Discrepancy between serology and small bowel histology, such as seronegative CD, poses a diagnostic challenge in celiac disease (CD) diagnosis. Recently described methods to detect gliadin-specific T-cells are too laborious even in a specialized diagnostic setting. We developed a method, which can be implemented in specialized diagnostic laboratories.

Gliadin-specific T-cells were analyzed by α1-and α2-gliadin peptide loaded Dextramers (Dm) in healthy controls (HC, n = 18), patients with non-celiac gluten sensitivity (NCGS, n = 9), active CD (aCD, n = 7) and CD on a gluten free diet (GFD, n = 14). Control peptide (CLIP)-loaded Dm were used as background controls. The α-gliadin-Dm:CLIP-Dm ratio was calculated. In CD patients ≥5 years on GFD (n = 8), a randomized two-dose gluten challenge was performed to increase gliadin-specific T-cell frequencies.

Gliadin-specific CD4+ T-cell frequencies were significantly higher in aCD and GFD than in HC and NCGS (p ≤ 0.0001). In CD patients on a GFD ≥5 years, gliadin-specific T-cells were detectable in 6/8 patients after a week gluten challenge, and all tested positive within 4 weeks. Gliadin-specific T-cells significantly upregulated CD38 after 1 week of gluten ingestion (p < 0.008). Real world data from sixteen patients demonstrated the applicability of this test in diagnostic challenging cases.

Gliadin-specific T-cells can be detected in peripheral blood of CD patients using commercially available dextramers. These cells persist in CD patients on a GFD but may decline over time. A short term low-dose gluten challenge increased sensitivity. This simplified detection method of gliadin-specific T-cells is suitable for diagnostic challenging CD cases.

•Dextramers can detect peripheral blood gliadin-specific CD4+ T-cells with a straightforward flowcytometry analysis method.•Gliadin-specific T-cell frequency was significantly higher in CD patients compared to controls (p < 0.0001).•A low-dose gluten challenge can increase gliadin-specific T-cells to detectable levels when undetectable pre-challenge.•Gliadin-specific T-cell detection can aid in diagnosis of challenging clinical cases such as seronegative CD.

Dextramers can detect peripheral blood gliadin-specific CD4+ T-cells with a straightforward flowcytometry analysis method.

Gliadin-specific T-cell frequency was significantly higher in CD patients compared to controls (p < 0.0001).

A low-dose gluten challenge can increase gliadin-specific T-cells to detectable levels when undetectable pre-challenge.

Gliadin-specific T-cell detection can aid in diagnosis of challenging clinical cases such as seronegative CD.

## Linked entities

- **Proteins:** CD4 (CD4 molecule), CD38 (CD38 molecule)
- **Diseases:** celiac disease (MONDO:0005130)

## Full-text entities

- **Genes:** CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}, BCL2A1 (BCL2 related protein A1) [NCBI Gene 597] {aka ACC-1, ACC-2, ACC1, ACC2, BCL2L5, BFL1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** CD (MESH:D002446), sensitivity (MESH:D003807)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12329281/full.md

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Source: https://tomesphere.com/paper/PMC12329281