Regulatory T-cell function is impaired in celiac disease

Marilena Granzotto, Sara Dal Bo, Sara Quaglia, Alberto Tommasini, Elisa Piscianz, Erica Valencic, Fortunato Ferrara, Stefano Martelossi, Alessandro Ventura, Tarcisio Not

Research output: Contribution to journalArticlepeer-review


Celiac disease (CD) is characterized by intolerance to gluten and high risk of developing autoimmune phenomena. Possible defects in immune tolerance could have a role in the pathogenesis of the disease. As regulatory T-cells (Tregs) are the main population involved in maintaining peripheral tolerance, we investigated the number of these cells in celiac patients as compared with healthy donors. Moreover, we analyzed the suppressive function of CD4+CD25+ T-cells from celiac disease patients and controls on autologous responder T-cells (CD4+CD25-). The percentage of CD4+CD25+FOXP3+ cells was not different in celiacs and in healthy controls, and among positive cells the level of expression of the two regulatory markers was comparable. However, the suppressor activity of Tregs was significantly impaired in CD patients. These results suggest that a defect in Tregs function could play a role in the pathogenesis of CD and in CD-associated autoimmunity.

Original languageEnglish
Pages (from-to)1513-1519
Number of pages7
JournalDigestive Diseases and Sciences
Issue number7
Publication statusPublished - Jul 2009


  • Autoimmunity
  • Celiac disease
  • Regulatory T-cells

ASJC Scopus subject areas

  • Gastroenterology
  • Physiology


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