RAR相关孤儿受体γ
白细胞介素17
外周血单个核细胞
白细胞介素23
白细胞介素
免疫学
免疫荧光
内分泌学
发病机制
医学
内科学
癌症研究
炎症
化学
细胞因子
FOXP3型
免疫系统
抗体
体外
生物化学
作者
Ai Yan,Ying Zhang,Xiaocong Wang,Yueling Cui,Wei Tan
出处
期刊:Bioengineered
[Informa]
日期:2022-05-02
卷期号:13 (5): 13293-13299
被引量:7
标识
DOI:10.1080/21655979.2022.2080367
摘要
T helper 17 (Th17) cells regulate inflammatory processes and are implicated in pathogenesis of proliferative diabetic retinopathy (PDR) through modulation of interleukin-17 (IL-17). IL-35, anti-inflammatory factor, negatively mediates IL-17 expression and Th17 differentiation. In this study, the role of IL-35 in PDR was assessed. The results showed that IL-35 was down-regulated, while IL-17 was up-regulated, in peripheral blood mononuclear cells (PBMCs) of PDR patients. In addition, immunofluorescence analysis indicated that frequency of Th17 cells was enhanced in the PBMCs of PDR patients. However, incubation with IL-35 reduced the Th17 cell frequency and decreased the level of IL-17 in CD4+ T lymphocytes. Moreover, the levels of transcription factors essential for Th17 differentiation, ROR α (retinoid-related orphan receptor alpha) and ROR γt, were reduced by IL-35 treatment. In conclusion, IL-35 reduced level of IL-17 and inhibited Th17 differentiation to protect against PDR.
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