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Circulating gluten-specific FOXP3

Authors :
Laura, Cook
C Mee Ling, Munier
Nabila, Seddiki
David, van Bockel
Noé, Ontiveros
Melinda Y, Hardy
Jana K, Gillies
Megan K, Levings
Hugh H, Reid
Jan, Petersen
Jamie, Rossjohn
Robert P, Anderson
John J, Zaunders
Jason A, Tye-Din
Anthony D, Kelleher
Source :
The Journal of allergy and clinical immunology. 140(6)
Publication Year :
2015

Abstract

Celiac disease is a chronic immune-mediated inflammatory disorder of the gut triggered by dietary gluten. Although the effector T-cell response in patients with celiac disease has been well characterized, the role of regulatory T (Treg) cells in the loss of tolerance to gluten remains poorly understood.We sought to define whether patients with celiac disease have a dysfunction or lack of gluten-specific forkhead box protein 3 (FOXP3)Treated patients with celiac disease underwent oral wheat challenge to stimulate recirculation of gluten-specific T cells. Peripheral blood was collected before and after challenge. To comprehensively measure the gluten-specific CD4Numbers of circulating gluten-specific Treg cells and effector T cells both increased significantly after oral wheat challenge, peaking at day 6. Surprisingly, we found that approximately 80% of the ex vivo circulating gluten-specific CD4This study provides the first estimation of FOXP3

Details

ISSN :
10976825
Volume :
140
Issue :
6
Database :
OpenAIRE
Journal :
The Journal of allergy and clinical immunology
Accession number :
edsair.pmid..........de2029412ae405666210cfdeb0cb0a1b