CÚRAM Centre for Research in Medical Devices, School of Medicine, Regenerative Medicine Institute (REMEDI), College of Medicine, Nursing and Health Sciences, National University of Ireland, Galway, Ireland.
Nephrology Services, Saolta University Healthcare Group, Galway, Ireland.
Front Immunol. 2018 Dec 6;9:2845. doi: 10.3389/fimmu.2018.02845. eCollection 2018.
Chronic kidney disease (CKD) affects 11-13% of the world's population and greatly increases risk of atherosclerotic cardiovascular disease (ASCVD) and death. It is characterized by systemic inflammation and disturbances in the blood leukocytes that remain incompletely understood. In particular, abnormalities in the numbers and relative proportions of the three major monocyte subsets-classical, intermediate, and non-classical-are described in CKD and end-stage renal disease. In this study, we characterized absolute numbers of blood leukocyte subtypes in adults with renal function varying from normal to advanced CKD. The primary aim was to identify monocyte subpopulations that associated most closely with current estimated glomerular filtration rate (eGFR) and subsequent rate of eGFR decline. Leucocyte and monocyte populations were enumerated by multi-color flow cytometry of whole blood and peripheral blood mononuclear cell (PBMC) samples from adults with CKD stage 1-5 ( = 154) and healthy adults ( = 33). Multiple-linear regression analyses were performed to identify associations between numbers of leucocyte and monocyte populations and clinical characteristics including eGFR and rate of eGFR decline with adjustment for age and gender. In whole blood, total monocyte and neutrophil, but not lymphocyte, numbers were higher in adults with CKD 1-5 compared to no CKD and were significantly associated with current eGFR even following correction for age. In PBMC, classical and intermediate monocyte numbers were higher in CKD 1-5 but only intermediate monocyte numbers were significantly associated with current eGFR in an age-corrected analysis. When intermediate monocytes were further sub-divided into those with mid- and high-level expression of class II MHC (HLA-DR and HLA-DR intermediate monocytes) it was found that only DR intermediate monocytes were increased in number in CKD 1-5 compared to no CKD and were significantly associated with eGFR independently of age among the total (No CKD + CKD 1-5) study cohort as well as those with established CKD (CKD 1-5 only). Furthermore, blood number of DR intermediate monocytes alone proved to be significantly associated with subsequent rate of renal functional decline. Together, our data confirm neutrophil and monocyte subset dysregulation in CKD and identify a distinct subpopulation of intermediate monocytes that is associated with higher rate of loss of kidney function.
慢性肾脏病(CKD)影响全球 11-13%的人口,极大地增加了动脉粥样硬化性心血管疾病(ASCVD)和死亡的风险。其特征是全身性炎症和血液白细胞的紊乱,但这些仍未得到充分理解。特别是在 CKD 和终末期肾病中,描述了三种主要单核细胞亚群-经典型、中间型和非经典型的数量和相对比例的异常。在这项研究中,我们对肾功能从正常到 CKD 晚期的成年人的血液白细胞亚型的绝对数量进行了特征描述。主要目的是确定与当前估计肾小球滤过率(eGFR)最密切相关的单核细胞亚群,以及随后的 eGFR 下降速度。通过对 CKD 1-5 期(n=154)和健康成年人(n=33)的全血和外周血单个核细胞(PBMC)样本进行多色流式细胞术,对白细胞和单核细胞进行了计数。进行了多元线性回归分析,以确定白细胞和单核细胞数量与临床特征(包括 eGFR 和 eGFR 下降速度)之间的关系,这些特征包括年龄和性别调整。在全血中,与无 CKD 相比,CKD 1-5 期的成年人单核细胞总数和中性粒细胞数量较高,但淋巴细胞数量没有差异,并且与当前的 eGFR 显著相关,即使在年龄校正后也是如此。在 PBMC 中,CKD 1-5 期的经典和中间单核细胞数量较高,但仅中间单核细胞数量与年龄校正后的当前 eGFR 显著相关。当将中间单核细胞进一步细分为具有中等和高水平表达 II 类 MHC(HLA-DR 和 HLA-DR 中间单核细胞)的细胞亚群时,发现只有 CKD 1-5 期的中间单核细胞数量增加,与无 CKD 相比,与年龄无关,并且在总(无 CKD+CKD 1-5)研究队列中以及已经患有 CKD(仅 CKD 1-5)的队列中,eGFR 与年龄无关。此外,DR 中间单核细胞的血液数量单独证明与随后的肾功能下降速度显著相关。总之,我们的数据证实了 CKD 中的中性粒细胞和单核细胞亚群失调,并确定了与肾功能丧失速度较高相关的独特中间单核细胞亚群。