Author/Authors :
Tye-Din، نويسنده , , Jason A. and Anderson، نويسنده , , Robert P. and Ffrench، نويسنده , , Rosemary A. and Brown، نويسنده , , Gregor J. and Hodsman، نويسنده , , Peter M. Siegel، نويسنده , , Matthew and Botwick، نويسنده , , Wendy and Shreeniwas، نويسنده , , Revati Shreeniwas، نويسنده ,
Abstract :
Effective treatment of celiac disease is an unmet medical need. A glutenase that destroys immunogenic gluten peptides may be clinically valuable. Twenty patients with celiac disease were randomly assigned to ingest a large gluten meal (16 g daily for 3 days) pre-treated with ALV003, a mixture of highly specific glutenases (n = 10), or pre-treated with placebo (n = 10). Peripheral blood T-cell IFN-γ ELISpot responses to gliadin and an immunogenic 33mer and symptoms were assessed. While baseline IFN-γ ELISpot responses to gliadin and the 33mer were negative in all patients, a significant ELISpot response to gliadin or the 33mer was observed in 6 of 10 patients consuming placebo-treated gluten and 0 of 10 consuming ALV003 pre-treated gluten (p = 0.011). Symptoms typically associated with gluten ingestion occurred in both groups and were not significantly reduced by ALV003 pre-treatment. ALV003 pre-treatment can abolish immune responses induced by gluten in patients with celiac disease.
Keywords :
Mucosal immunology , Celiac disease , gluten , IFN-? ELISpot , Enzymology