Low-dose IL-2 expands CD4+ regulatory T cells with a suppressive function in vitro via the STAT5-dependent pathway in patients with chronic kidney diseases. (15th October 2018)

• Record Type: Journal Article
• Authors: Li, Yuanyuan; Liu, Xueyong; Wang, Wei; Wang, Shaohua; Zhang, Jianchun; Jiang, Song; Wang, Yang; Li, Liping; Li, Jinghua; Zhang, Youkang; Huang, Haichang
• Is Part Of: Renal failure. Volume 40:Number 1(2018)
• Page Start: 280
• Page End: 288
• Publication Date: 2018-10-15
• Subjects: Chronic kidney disease -- glomerulonephritis -- cytokines -- lymphocytes -- signaling; Chronic renal failure -- Periodicals; Acute renal failure -- Periodicals; Uremia -- Periodicals; 616.614005
• DOI: 10.1080/0886022X.2018.1456462
• Languages: English
• ISSNs: 0886-022X

Abstract

Abstract: Background: Patients with chronic kidney disease (CKD) often have CD4+ regulatory T cells (Tregs) dysfunction and chronic inflammation. We aim to investigate the effect, function, and related mechanism of low-dose IL-2 on CD4 + regulatory T cells expansion in vitro from patients with CKD. Methods: A total of 148 newly diagnosed patients with CKD at Stage III and 35 healthy volunteer subjects were recruited into our studies. The number of peripheral Tregs in peripheral blood mononuclear cells isolated from CKD patients, which were characterized by FACS as CD4 + CD25 hi and CD4 + CD25 + FoxP3 + . The effect of low-dose IL-2 on expansion of Tregs, and the suppressive function of expanded Tregs were also analyzed by FACS. The levels of FoxP3 mRNA were detected by qRT-PCR. The activation of IL-2 induced Stat5 and blocking experiments were assessed by Western Blotting and FACS. Results: We found that the frequency of peripheral Tregs from CKD patients was significantly lower than that in healthy volunteer subjects. We also showed that IL-2 selectively expanded CD4 + CD25 hi and CD4 + CD25 + FoxP3 + regulatory T cells, and also upregulated the expression of FoxP3 mRNA. Our in vitro studies demonstrated that expanded CD4 + regulatory T cells from CKD patients suppressed proinflammatory Th1 and Th17 cell response. Furthermore, STAT5 activation is required for IL-2-induced expansion of regulatory T cells and expression of FoxP3 mRNA from CKD patients. Conclusions: Our findings support the clinical Treg defects in CKD patients with glomerular diseases, and the rationale of evaluating low-dose IL-2 treatment for selectively modulating CD4 + Tregs.