Unknown

Dataset Information

0

Deficiency of immunoregulatory indoleamine 2,3-dioxygenase 1in juvenile diabetes.


ABSTRACT: A defect in indoleamine 2,3-dioxygenase 1 (IDO1), which is responsible for immunoregulatory tryptophan catabolism, impairs development of immune tolerance to autoantigens in NOD mice, a model for human autoimmune type 1 diabetes (T1D). Whether IDO1 function is also defective in T1D is still unknown. We investigated IDO1 function in sera and peripheral blood mononuclear cells (PBMCs) from children with T1D and matched controls. These children were further included in a discovery study to identify SNPs in IDO1 that might modify the risk of T1D. T1D in children was characterized by a remarkable defect in IDO1 function. A common haplotype, associated with dysfunctional IDO1, increased the risk of developing T1D in the discovery and also confirmation studies. In T1D patients sharing such a common IDO1 haplotype, incubation of PBMCs in vitro with tocilizumab (TCZ) - an IL-6 receptor blocker - would, however, rescue IDO1 activity. In an experimental setting with diabetic NOD mice, TCZ was found to restore normoglycemia via IDO1-dependent mechanisms. Thus, functional SNPs of IDO1 are associated with defective tryptophan catabolism in human T1D, and maneuvers aimed at restoring IDO1 function would be therapeutically effective in at least a subgroup of T1D pediatric patients.

SUBMITTER: Orabona C 

PROVIDER: S-EPMC5926942 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Deficiency of immunoregulatory indoleamine 2,3-dioxygenase 1in juvenile diabetes.

Orabona Ciriana C   Mondanelli Giada G   Pallotta Maria T MT   Carvalho Agostinho A   Albini Elisa E   Fallarino Francesca F   Vacca Carmine C   Volpi Claudia C   Belladonna Maria L ML   Berioli Maria G MG   Ceccarini Giulia G   Esposito Susanna Mr SM   Scattoni Raffaella R   Verrotti Alberto A   Ferretti Alessandra A   De Giorgi Giovanni G   Toni Sonia S   Cappa Marco M   Matteoli Maria C MC   Bianchi Roberta R   Matino Davide D   Iacono Alberta A   Puccetti Matteo M   Cunha Cristina C   Bicciato Silvio S   Antognelli Cinzia C   Talesa Vincenzo N VN   Chatenoud Lucienne L   Fuchs Dietmar D   Pilotte Luc L   Van den Eynde Benoît B   Lemos Manuel C MC   Romani Luigina L   Puccetti Paolo P   Grohmann Ursula U  

JCI insight 20180322 6


A defect in indoleamine 2,3-dioxygenase 1 (IDO1), which is responsible for immunoregulatory tryptophan catabolism, impairs development of immune tolerance to autoantigens in NOD mice, a model for human autoimmune type 1 diabetes (T1D). Whether IDO1 function is also defective in T1D is still unknown. We investigated IDO1 function in sera and peripheral blood mononuclear cells (PBMCs) from children with T1D and matched controls. These children were further included in a discovery study to identify  ...[more]

Similar Datasets

| S-EPMC4553081 | biostudies-literature
| S-EPMC7935521 | biostudies-literature
| S-EPMC4368142 | biostudies-literature
| S-EPMC9786828 | biostudies-literature
| S-EPMC6318801 | biostudies-literature
| S-EPMC5522192 | biostudies-literature
| S-EPMC3441469 | biostudies-literature
| S-EPMC1221754 | biostudies-other
| S-EPMC3645912 | biostudies-literature
| S-EPMC3190733 | biostudies-literature