Author/Authors :
Matthew Siegel، نويسنده , , Michael T. Bethune، نويسنده , , Jonathan Gass، نويسنده , , Jennifer Ehren، نويسنده , , Jiang Xia، نويسنده , , Alexandre Johannsen، نويسنده , , Tor B. Stuge، نويسنده , , Gary M. Gray، نويسنده , , Peter P. Lee، نويسنده , , Chaitan Khosla، نويسنده ,
Abstract :
Celiac sprue (also known as celiac disease) is an inheritable, gluten-induced enteropathy of the upper small intestine with an estimated prevalence of 0.5%–1% in most parts of the world. The ubiquitous nature of food gluten, coupled with inadequate labeling regulations in most countries, constantly poses a threat of disease exacerbation and relapse for patients. Here, we demonstrate that a two-enzyme cocktail comprised of a glutamine-specific cysteine protease (EP-B2) that functions under gastric conditions and a PEP, which acts in concert with pancreatic proteases under duodenal conditions, is a particularly potent candidate for celiac sprue therapy. At a gluten:EP-B2:PEP weight ratio of 75:3:1, grocery store gluten is fully detoxified within 10 min of simulated duodenal conditions, as judged by chromatographic analysis, biopsy-derived T cell proliferation assays, and a commercial antigluten antibody test.