| Literature DB >> 28277888 |
Harald Hundsberger1, Anita Koppensteiner1, Elisabeth Hofmann1, Doris Ripper1, Maren Pflüger1, Valerie Stadlmann2, Christian Theodor Klein1, Birgit Kreiseder1, Michael Katzlinger3, Andreas Eger1, Florian Forster2, Albert Missbichler2, Christoph Wiesner1.
Abstract
Celiac disease (CD) is a chronic inflammatory condition caused by the ingestion of gliadin-containing food in genetically susceptible individuals. Undigested peptides of gliadin exert various effects, including increased intestinal permeability and inflammation in the small intestine. Although many therapeutic approaches are in development, a gluten-free diet is the only effective treatment for CD. Affecting at least 1% of the population in industrialized countries, it is important to generate therapeutic options against CD. Here, we describe the establishment of a high-throughput screening (HTS) platform based on AlphaLISA and electrical cell-substrate impedance sensing (ECIS) technology for the identification of anti-inflammatory and barrier-protective compounds in human enterocytes after pepsin-trypsin-digested gliadin (PT-gliadin) treatment. Our results show that the combination of these HTS technologies enables fast, reliable, simple, and label-free screening of IgY antibodies against PT-gliadin. Using this platform, we have identified a new chicken anti-PT-gliadin IgY antibody as a potential anti-CD agent.Entities:
Keywords: AlphaLISA; Caco-2 monolayer; ECIS; anti-gliadin IgY; celiac disease
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Year: 2017 PMID: 28277888 DOI: 10.1177/2472555217697435
Source DB: PubMed Journal: SLAS Discov ISSN: 2472-5552 Impact factor: 3.341