Author/Authors :
DʹAngelo، نويسنده , , Sara and Mignone، نويسنده , , Flavio and Deantonio، نويسنده , , Cecilia and Di Niro، نويسنده , , Roberto and Bordoni، نويسنده , , Roberta and Marzari، نويسنده , , Roberto and De Bellis، نويسنده , , Gianluca and Not، نويسنده , , Tarcisio and Ferrara، نويسنده , , Fortunato and Bradbury، نويسنده , , Andrew and Santoro، نويسنده , , Claudio and Sblattero، نويسنده , , Daniele، نويسنده ,
Abstract :
The aim of this study was to dissect the autoantibody response in celiac disease (CD) that remains largely unknown, with the goal of identifying the disease-specific autoantigenic protein pattern or the so called epitome. Sera from CD patients were used to select immunoreactive antigens from a cDNA phage-display library. Candidate genes were identified, the corresponding proteins produced and their immunoreactivity validated with sera from CD patients and controls. Thirteen CD-specific antigens were identified and further validated by protein microarray. The specificity for 6 of these antigens was confirmed by ELISA. Furthermore we showed that this antibody response was not abolished on a gluten free diet and was not shared with other autoimmune diseases. These antigens appear to be CD specific and independent of gluten induction. The utility of this panel extends beyond its diagnostic value and it may drive the attention to new targets for unbiased screens in autoimmunity research.
Keywords :
Autoantibody , Autoantigen , ORF-display libraries , next generation sequencing , Celiac disease , Protein microarray