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Gluten-sensitive enteropathy coincides with decreased capability of intestinal T cells to secrete IL-17 and IL-22 in a macaque model for celiac disease.

Abstract
Celiac disease (CD) is an autoimmune disorder caused by intolerance to dietary gluten. The interleukin (IL)-17 and IL-22 function as innate regulators of mucosal integrity. Impaired but not well-understood kinetics of the IL-17/22 secretion was described in celiac patients. Here, the IL-17 and IL-22-producing intestinal cells were studied upon their in vitro stimulation with mitogens in class II major histocompatibility complex-defined, gluten-sensitive rhesus macaques. Pediatric biopsies were collected from distal duodenum during the stages of disease remission and relapse. Regardless of dietary gluten content, IL-17 and IL-22-producing cells consisted of CD4+ and CD8+ T lymphocytes as well as of lineage-negative (Lin-) cells. Upon introduction of dietary gluten, capability of intestinal T cells to secrete IL-17/22 started to decline (p<0.05), which was paralleled with gradual disruption of epithelial integrity. These data indicate that IL-17/22-producing cells play an important role in maintenance of intestinal mucosa in gluten-sensitive primates.
AuthorsHuanbin Xu, Stephanie L Feely, Xiaolei Wang, David X Liu, Juan T Borda, Jason Dufour, Weiwei Li, Pyone P Aye, Gaby G Doxiadis, Chaitan Khosla, Ronald S Veazey, Karol Sestak
JournalClinical immunology (Orlando, Fla.) (Clin Immunol) Vol. 147 Issue 1 Pg. 40-49 (Apr 2013) ISSN: 1521-7035 [Electronic] United States
PMID23518597 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
CopyrightCopyright © 2013 Elsevier Inc. All rights reserved.
Chemical References
  • Interleukin-17
  • Interleukins
  • Glutens
Topics
  • Animals
  • CD4-Positive T-Lymphocytes (immunology, metabolism)
  • CD8-Positive T-Lymphocytes (immunology, metabolism)
  • Celiac Disease (immunology, metabolism)
  • Disease Models, Animal
  • Duodenum (immunology, metabolism, pathology)
  • Flow Cytometry
  • Glutens (immunology)
  • Humans
  • Interleukin-17 (immunology, metabolism)
  • Interleukins (immunology, metabolism)
  • Intestinal Mucosa (immunology, metabolism, pathology)
  • Intestines (immunology, pathology)
  • Lymphocyte Count
  • Macaca mulatta
  • Microscopy, Confocal
  • T-Lymphocytes (immunology, metabolism)
  • Interleukin-22

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