| Literature DB >> 30635394 |
Sara Quaglia1, Fortunato Ferrara2, Luigina De Leo1, Fabiana Ziberna1, Serena Vatta1, Serena Marchiò3,4, Daniele Sblattero5, Alessandro Ventura1,5, Tarcisio Not6,5.
Abstract
An unbalance between Abs that recognize an autoantigen (idiotypes; IDs) and Igs that bind such Abs (anti-IDs) is considered a functional event in autoimmune disorders. We investigated the presence of an ID/anti-ID network in celiac disease (CD), a condition in which antitissue transglutaminase 2 (TG2) Abs are suspected to contribute to CD pathogenesis. To characterize the ID side, we reproduced by in vitro yeast display the intestine-resident Abs from CD and control patients. These TG2-specific IDs were used to identify potential anti-IDs in the serum. We observed elevated titers of anti-IDs in asymptomatic patients with predisposition to CD and demonstrated that anti-ID depletion from the serum restores a detectable humoral response against TG2. Our study provides an alternative approach to quantify CD-related autoantibodies in cases that would be defined "negative serology" with current diagnostic applications. Therefore, we suggest that developments of this technology could be designed for perspective routine tests.Entities:
Mesh:
Substances:
Year: 2019 PMID: 30635394 DOI: 10.4049/jimmunol.1800819
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422