Clinical Testing of Gliadin Fractions in Coeliac Patients

Author:

Ciclitira P. J.1,Evans D. J.2,Fagg N. L. K.3,Lennox E. S.4,Dowling R. H.1

Affiliation:

1. Gastroenterology Unit, Department of Medicine, Guy's Hospital, London

2. Department of Histopathology, Hammersmith Hospital, London

3. Department of Histopathology, Guy's Hospital, London

4. MRC Laboratory of Molecular Biology, Cambridge, U.K.

Abstract

1. Since the toxic fraction of cereal flour which damages the small bowel mucosa of patients with coeliac disease has not been fully defined in vivo, we studied the effect of intraduodenal infusions of different doses of unfractionated gliadin and of α-, β-, γ- and ω-gliadin subfractions on the morphology of multiple jejunal biopsies taken from two patients with treated coeliac disease. 2. A dose-response study with increasing quantities of unfractionated gliadin in one coeliac patient showed that 1000 mg produced marked damaged in serial jejunal biopsies taken 2–3 h after commencing the infusion and that the changes had almost completely disappeared 72 h later. 3. α-, β-, γ- and ω-gliadin were prepared, checked for purity and investigated for toxicity in two coeliac patients. After an intraduodenal challenge with 1000 mg of the four gliadin sub-fractions these were shown to have induced damage in the mucosa of jejunal biopsies taken 6 h later. 4. These observations confirm the results of studies in vitro, which suggest that not only α- but β-, γ- and ω-gliadin are enterotoxic in coeliac disease.

Publisher

Portland Press Ltd.

Subject

General Medicine

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