Human glycoprotein-2 expressed in Brunner glands – A putative autoimmune target and link between Crohn's and coeliac disease

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Dirk Roggenbuck - , Brandenburg University of Technology (Autor:in)
  • Alexander Goihl - , Otto von Guericke University Magdeburg (Autor:in)
  • Mandy Sowa - , GA Generic Assays GmbH (Autor:in)
  • Steffi Lopens - , Medipan GmbH (Autor:in)
  • Stefan Rödiger - , Brandenburg University of Technology (Autor:in)
  • Peter Schierack - , Brandenburg University of Technology (Autor:in)
  • Karsten Conrad - , Institut für Immunologie (Autor:in)
  • Ulrich Sommer - , Institut für Pathologie (Autor:in)
  • Korinna Jöhrens - , Institut für Pathologie, Universitätsklinikum Carl Gustav Carus Dresden (Autor:in)
  • Robert Grützmann - , Friedrich-Alexander-Universität Erlangen-Nürnberg (Autor:in)
  • Dirk Reinhold - , Otto von Guericke University Magdeburg (Autor:in)
  • Martin W. Laass - , Klinik und Poliklinik für Kinder- und Jugendmedizin, Universitätsklinikum Carl Gustav Carus Dresden (Autor:in)

Abstract

Glycoprotein 2 (GP2) is an autoantigen in Crohn's (CD) and coeliac disease (CeD). We assessed GP2-isoform (GP21–4)-expression in intestinal biopsies of paediatric patients with CD, CeD, ulcerative colitis (UC), and healthy children (HC). Transcription of GP21–4 was elevated in proximal small intestine in CeD and CD patients (only GP22/4) compared to jejunum (CeD/CD) and large bowel (CD). CeD patients demonstrated higher duodenal GP22/4-mRNA levels compared to HC/UC patients whereas CD patients showed higher GP24-mRNA levels compared to UC patients. Duodenal synthesis of only small GP2 isoforms (GP23/4) was demonstrated in epithelial cells in patients/HC and in Brunner glands (also large isoforms) with a more frequent apical location in CD/CeD patients. All four GP2 isoforms interacted with gliadin and phosphopeptidomannan. Gliadin digestion improved binding to GP2 isoforms. GP21–4 binding to CeD/CD-related antigens, elevated duodenal GP21–4-mRNA transcription, and GP2-protein secretion in Brunner glands of CeD/CD patients suggest an autoimmune CeD/CD link.

Details

OriginalspracheEnglisch
Aufsatznummer109214
FachzeitschriftClinical immunology
Jahrgang247
PublikationsstatusVeröffentlicht - Feb. 2023
Peer-Review-StatusJa

Externe IDs

PubMed 36608744

Schlagworte

Ziele für nachhaltige Entwicklung

Schlagwörter

  • Celiac disease, Crohn's disease, Zymogen granule membrane glycoprotein GP2