| Literature DB >> 31013255 |
Chiara Donadei1,2, Andrea Angeletti1,2, Chiara Cantarelli1,3, Vivette D D'Agati4, Gaetano La Manna2, Enrico Fiaccadori3, Julian K Horwitz1, Huabao Xiong1, Chiara Guglielmo1, Susan Hartzell1, Joren C Madsen5, Umberto Maggiore3, Peter S Heeger1, Paolo Cravedi1.
Abstract
IL-17-producing CD4+ cells (TH17) are pathogenically linked to autoimmunity including to autoimmune kidney disease. Erythropoietin's (EPO) newly recognized immunoregulatory functions and its predominant intra-renal source suggested that EPO physiologically regulates TH17 differentiation, thereby serving as a barrier to the development of autoimmune kidney disease. Using in vitro studies of human and murine cells and in vivo models, we show that EPO ligation of its receptor (EPO-R) on CD4+ T cells directly inhibits TH17 generation and promotes trans-differentiation of TH17 into IL-17-FOXP3+CD4+ T cells. Mechanistically, EPO/EPO-R ligation abrogates upregulation of SGK1 gene expression and blocks p38 activity to prevent SGK1 phosphorylation, thereby inhibiting RORC-mediated transcription of IL-17 and IL-23 receptor genes. In a murine model of TH17-dependent aristolochic acid (ArA)-induced, interstitial kidney disease associated with reduced renal EPO production, we demonstrate that transgenic EPO overexpression or recombinant EPO (rEPO) administration limits TH17 formation and clinical/histological disease expression. EPO/EPO-R ligations on CD4+ T cells abrogate, while absence of T cell-expressed EPO-R augments, TH17 induction and clinical/histological expression of pristane-induced glomerulonephritis (associated with decreased intrarenal EPO). rEPO prevents spontaneous glomerulonephritis and TH17 generation in MRL-lpr mice. Together, our findings indicate that EPO physiologically and therapeutically modulate TH17 cells to limit expression of TH17-associated autoimmune kidney disease.Entities:
Keywords: Adaptive immunity; Immunology; Nephrology; T cells; Tolerance
Year: 2019 PMID: 31013255 PMCID: PMC6542617 DOI: 10.1172/jci.insight.127428
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708