外周血单个核细胞
2型糖尿病
白细胞介素2受体
Treg细胞
离子霉素
免疫学
超重
内分泌学
内科学
医学
体质指数
发病机制
CD28
糖尿病
CD3型
肥胖
效应器
生物
抗原
T细胞
免疫系统
CD8型
体外
生物化学
刺激
作者
Nancy Cortez-Espinosa,Juan D. Cortés-García,Ernesto Martínez-Leija,Jose Guillermo Rodríguez-Rivera,Carlos Barajas‐López,Roberto González‐Amaro,Diana Patricia Portales-Pérez
标识
DOI:10.1016/j.humimm.2015.09.007
摘要
Th17 cells are involved in the pathogenesis of multiple inflammatory diseases such as type two diabetes (T2D). CD39(+) Treg cells have been implicated as responsible for suppressing Th17 cells. The aim of this study was to evaluate the number and function of CD4(+)CD25(high)CD39(+) Treg and Th17 cells in peripheral blood mononuclear cells (PBMC) from T2D patients and healthy control subjects. The Th17 cells were detected in PBMC under culture with human anti-CD3/CD28 and PMA/ionomycin and the levels of IL-17 were assessed by ELISA and qPCR. The T2D patients with obesity showed significantly lower percentages of CD39(+) Treg cells. A negative correlation between CD39(+) Treg cells and weight, and body mass index was detected. In contrast, the low levels of CD4(+)IL-17(+) cells in overweight and obese T2D patients showed a positive correlation with glucose and HbA1c. Additionally, we found a subpopulation of Th17 cells that express CD39 and were correlated with glucose and HbA1c. Our findings suggest that the expression of CD39 on Treg cells and also in CD4(+)IL-17(+) cells from T2D patients is related to hyperglycemia as well as to overweight and obesity and therefore may participate as a modulator of the effector capacity of Th17 cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI