Adult-onset type 1 diabetes patients display decreased IGRP-specific Tr1 cells in blood

Daisuke Chujo, Thien Son Nguyen, Emile Foucat, Derek Blankenship, Jacques Banchereau, Gerald T. Nepom, Damien Chaussabel, Hideki Ueno

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

The breakdown of immune tolerance against islet antigens causes type 1 diabetes (T1D). The antigens associated with adult-onset T1D (AT1D) remain largely undefined. It is possible that AT1D patients display a unique type of CD4+ T cells specific for a certain islet antigen. Here we analyzed the cytokine production profiles of CD4+ helper T (Th) cells that are specific for three islet antigens; GAD65, preproinsulin, and IGRP in patients with AT1D, juvenile-onset T1D (JT1D), and age-, gender- and human leukocyte antigen (HLA)-matched control adults. While IGRP-specific Th cells in AT1D patients were dominantly Th1 cells, IGRP-specific Th cells in control adults and JT1D patients were dominantly Th2 and T regulatory type 1 (Tr1) cells. Notably, the frequency of IGRP-specific Tr1 cells was significantly lower in AT1D patients than in control adults and JT1D patients. In conclusion, our study suggests that IGRP-specific Th cells play a unique pathogenic role in AT1D.

Original languageEnglish
Pages (from-to)270-277
Number of pages8
JournalClinical Immunology
Volume161
Issue number2
DOIs
StatePublished - 1 Dec 2015
Externally publishedYes

Keywords

  • CD4 T cells
  • Islet antigens
  • Islet-specific glucose 6 phosphatase catalytic subunit-related protein
  • T regulatory type 1 (Tr1) cells
  • Type 1 diabetes

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