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ABSTRACT: Background
Certain immunotoxic peptides from gluten are resistant to gastrointestinal digestion and can interact with celiac-patient factors to trigger an immunologic response. A gluten-free diet (GFD) is the only effective treatment for celiac disease (CD), and its compliance should be monitored to avoid cumulative damage. However, practical methods to monitor diet compliance and to detect the origin of an outbreak of celiac clinical symptoms are not available.Objective
We assessed the capacity to determine the gluten ingestion and monitor GFD compliance in celiac patients by the detection of gluten and gliadin 33-mer equivalent peptidic epitopes (33EPs) in human feces.Design
Fecal samples were obtained from healthy subjects, celiac patients, and subjects with othe
SUBMITTER: Comino I
PROVIDER: S-EPMC3278243 | biostudies-literature | 2012 Mar
REPOSITORIES: biostudies-literature