Key result
Analysis of 100 Belgium beers using G12/A1 monoclonal antibodies estimated at least 20 ppm gluten equivalents in 90 beers and found 10 beers to be gluten-free.
The G12/A1 monoclonal antibody method is a practical and specific way to measure potential immunotoxicity of beers for celiac patients.
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BACKGROUND: Cereals used for beer manufacturing contain gluten, which is immunotoxic for celiac patients. The gluten remaining after processes of malting and brewing is mostly hydrolyzed, which makes practical evaluation of the immunotoxicity of the gluten pools challenging. RESULTS: We analyzed the presence of gluten peptides equivalent to the major immunotoxic protease-resistant gliadin 33-mer in 100 Belgium beers, using monoclonal antibodies (G12/A1). Immunochromatographic strips and enzyme-linked immonosorbent assay G12/A1 methods estimated at least 20 ppm gluten equivalents in 90 beers and gluten-free in 10 beers. The G12/A1 reactivity of beer high-performance liquid chromatographic fractions correlated to the presence of T-cell-reactive epitopes identified by peptide sequencing. CONCLUSION: The determination of equivalent gliadin 33-mer epitopes in beers has been shown to be practical, specific, and sensitive for the measurement of potential immunotoxicity for celiac patients.
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Beers may retain immunotoxic gluten peptides; leaves open safe consumption thresholds for celiac patients and needs clinical validation.
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Comino et al. (2012) studied Celiac disease (n=100). Immunological determination of gliadin 33-mer equivalent peptides was evaluated on Presence of gluten peptides equivalent to gliadin 33-mer. Analysis of 100 Belgium beers using G12/A1 monoclonal antibodies estimated at least 20 ppm gluten equivalents in 90 beers and found 10 beers to be gluten-free.
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