Key result
Polyclonal antibodies raised against 14 synthetic gluten peptides successfully discriminated wheat, barley, and oat prolamins during indirect ELISA assessments.
Why the study?
Current gluten immunoassays cannot discriminate gluten sources, causing inaccurate quantification and hindering compliance with food-labeling regulations for celiac disease.
Polyclonal antibodies raised against synthetic gluten peptides can successfully discriminate between wheat, barley, and oat prolamins, potentially improving food safety monitoring for celiac patients.
May advance gluten detection methods for celiac safety; leaves open translation from animal models to clinical use.
Celiac disease (CD) is triggered by ingestion of gluten-containing cereals such as wheat, barley, rye and in some cases oat. The only way for affected individuals to avoid symptoms of this condition is to adopt a gluten-free diet. Thus, gluten-free foodstuffs need to be monitored in order to ensure their innocuity. For this purpose, commercial immunoassays based on recognition of defined linear gluten sequences are currently used. These immunoassays are designed to detect or quantify total gluten regardless of the cereal, and often result in over or underestimation of the exact gluten content. In addition, Canadian regulations require a declaration of the source of gluten on the label of prepackaged foods, which cannot be done due to the limitations of existing methods. In this study, the development of new antibodies targeting discrimination of gluten sources was conducted using synthetic peptides as immunization strategy. Fourteen synthetic peptides selected from unique linear amino acid sequences of gluten were bioconjugated to Concholepas concholepas hemocyanin (CCH) as protein carrier, to elicit antibodies in rabbit. The resulting polyclonal antibodies (pAbs) successfully discriminated wheat, barley and oat prolamins during indirect ELISA assessments. pAbs raised against rye synthetic peptides cross-reacted evenly with wheat and rye prolamins but could still be useful to successfully discriminate gluten sources in combination with the other pAbs. Discrimination of gluten sources can be further refined and enhanced by raising monoclonal antibodies using a similar immunization strategy. A methodology capable of discriminating gluten sources, such as the one proposed in this study, could facilitate compliance with Canadian regulations on this matter. This type of discrimination could also complement current immunoassays by settling the issue of over and underestimation of gluten content, thus improving the safety of food intended to CD and wheat-allergic patients.
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Poirier et al. (2021) studied Celiac disease. Polyclonal antibodies from synthetic gluten peptides was evaluated on Discrimination of gluten sources via indirect ELISA. Polyclonal antibodies raised against 14 synthetic gluten peptides successfully discriminated wheat, barley, and oat prolamins during indirect ELISA assessments.
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