A Randomized Double-Blind, Placebo-Controlled Dose-Response Study to Assess the Gluten Threshold Dose in Celiac Disease
- Author(s)
- Daveson, AJM; Colgrave, ML; Craig, E; Vitak, A; Ware, RS; Schafer, J; Sehgal, A; Bose, U; Hardy, MY; Tye-Din, JA; Anderson, RP;
- Details
- Publication Year 2026-08,Volume 171,Issue #2,Page 285-297
- Journal Title
- Gastroenterology
- Abstract
- BACKGROUND & AIMS: Celiac disease is an immune-mediated enteropathy triggered by gluten ingestion. The effect of very small gluten exposures remains uncertain, contributing to international variations in food-labeling standards. Interleukin 2 (IL2) rises rapidly after gluten ingestion, serving as a biomarker of immune activation. We aimed to identify the lowest gluten dose that elicits a measurable IL2 response and accompanying symptoms in treated celiac disease. METHODS: We conducted a randomized double-blind, placebo-controlled adaptive dose-response trial in adults with biopsy-proven celiac disease on a gluten-free diet for >2 years. Participants (n = 51; median age, 52 years; 69% were female) underwent 3 oral gluten (1-1000 mg) or placebo challenges at 4-week intervals at a tertiary clinical trials center in Brisbane, Australia. The primary outcome was a >/=2-fold rise in serum IL2 within 6 hours. Secondary outcomes were patient-reported symptoms. Eliciting dose (ED(p), ie, the dose at which p% of people respond) was estimated by interval-censored survival analysis. RESULTS: Fifty-one participants completed 153 challenges. Gluten induced dose-dependent IL2 elevations, with >/=2-fold increases in 83% at 1000 mg, 83% at 610 mg, 36% at 90 mg, 17% at 13 mg, 27% at 8 mg, and 17% at 3 mg; none responded to 5 mg, 2 mg, 1 mg, or placebo. Estimated ED(50) was 111 mg (95% CI, 0-244 mg), ED(10) was 2.4 mg (95% CI, 0-5.3 mg), ED(05) was 0.8 mg (95% CI, 0-1.8 mg), and ED(01) was 0.1 mg (95% CI, 0.0-0.3 mg). Symptom scores increased after challenges but not beyond placebo. CONCLUSIONS: Acute IL2 release occurs at gluten doses below current food-labeling thresholds. Symptoms are unreliable at exposures <1000 mg. These findings provide a framework for defining exposure limits based on immune activation. (Australian and New Zealand Clinical Trials Registry, Number: 12621000781842).
- Publisher
- Elsevier
- Keywords
- Humans; *Celiac Disease/immunology/diet therapy/blood/diagnosis; Female; Middle Aged; Double-Blind Method; *Glutens/administration & dosage/immunology/adverse effects; Male; *Interleukin-2/blood; Adult; Aged; Diet, Gluten-Free; Biomarkers/blood; Dose-Response Relationship, Drug; Administration, Oral; Time Factors; Treatment Outcome; Celiac Disease; Eliciting Dose; Interleukin 2
- Research Division(s)
- Immunology
- PubMed ID
- 41903816
- Publisher's Version
- https://doi.org/10.1053/j.gastro.2026.03.011
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2026-04-27 02:50:38
Last Modified: 2026-07-30 09:26:01