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Indoleamine 2,3-Dioxygenase (IDO) Regulates Th17/Treg Immunity in Experimental IgA Nephropathy.

Abstract
IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide. Current studies have shown that the Th17/Treg immune balance may be involved in the occurrence of IgAN, but the exact mechanism is still unclear. Indoleamine 2,3-dioxygenase (IDO) is an enzyme that catalyses degradation of tryptophan (Trp) through the kynurenine (Kyn) pathway; it can control inflammation and immune response by inducing Trp starvation. IDO may be a key molecule in regulating the Th17/Treg immune balance. However, it is not clear whether IDO is involved in the IgAN disease occurrence by regulating the Th17/Treg immune balance. In this study, an IgAN mouse model was established. The mice were intraperitoneally inoculated with IDO inhibitor 1-MT or agonist ISS-ODN to observe whether the IDO signalling pathway participates in the occurrence and development of IgAN by regulating the Th17/Treg immune balance. The results showed that IDO inhibitor 1-MT significantly increased renal injury and glomerular IgA accumulation and up-regulated Th17/Treg and Th17-related cytokine expression in IgAN mice, while ISS-ODN significantly decreased renal injury and glomerular IgA accumulation, down-regulated Th17/Treg expression and inhibited Th17-related cytokine expression in IgAN mice. In conclusion, IDO was involved in the occurrence and progress of IgAN by regulating the Th17/ Treg balance.
AuthorsY Yang, K Liu, Y Chen, Y Gong, Y Liang
JournalFolia biologica (Folia Biol (Praha)) Vol. 65 Issue 2 Pg. 101-108 ( 2019) ISSN: 0015-5500 [Print] Czech Republic
PMID31464185 (Publication Type: Journal Article)
Chemical References
  • Cytokines
  • Indoleamine-Pyrrole 2,3,-Dioxygenase
Topics
  • Animals
  • Cytokines (metabolism)
  • Female
  • Glomerulonephritis, IGA (enzymology, immunology)
  • Immunity
  • Indoleamine-Pyrrole 2,3,-Dioxygenase (metabolism)
  • Kidney (injuries, metabolism, pathology)
  • Mice, Inbred BALB C
  • Signal Transduction
  • T-Lymphocytes, Regulatory (immunology)
  • Th17 Cells (immunology)

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