Department of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, Thessaloniki, Greece.
Department of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, Thessaloniki, Greece.
Clin Immunol. 2020 Jun;215:108423. doi: 10.1016/j.clim.2020.108423. Epub 2020 Apr 15.
Aim of the present study was to investigate the possible involvement of TNF-α signaling pathway and T-lymphocyte activation in DN. Eighty-two diabetic patients [39 male, age 69.5(56-78)years] were divided into three groups, according to Albumin/Creatinine ratio (ACR) levels, Group I (ACR < 30 μg/mg), Group II (ACR 30-300 μg/mg), Group III (ACR > 300 μg/mg). Urinary Tumor Necrosis Factor-α (TNF-α), and serum TNF-α, ΤNF-receptor 1 (TNFR1), TNFR2, B7-1, CD28, Cytoxic T-Lymphocyte-Associated protein-4 (CTLA4), were estimated. There were significant differences between Groups I, II, III regarding the concentration of urinary TNF-α (p < .001), serum TNFR1 (p < .001), serum TNFR2(p < .001), CTLA4 (p < .001) and CD28(p = .034). In multivariate analysis, independent parameters correlated with ACR were serum TNFR1 (p = .003), TNFR2 (p = .012) and urinary TNF-α (p = .015) levels. There was a significant correlation between markers of T-cell activation and TNF-α signaling pathway activation. Activation of TNF-α signaling pathway and T-lymphocytes seem to synergize and participate in the development of DN in type II DM.
本研究旨在探讨 TNF-α 信号通路和 T 淋巴细胞活化在糖尿病肾病(DN)中的可能作用。82 例糖尿病患者[39 例男性,年龄 69.5(56-78)岁]根据白蛋白/肌酐比值(ACR)水平分为三组,组 I(ACR<30μg/mg),组 II(ACR 30-300μg/mg),组 III(ACR>300μg/mg)。测定尿肿瘤坏死因子-α(TNF-α)和血清 TNF-α、TNF 受体 1(TNFR1)、TNFR2、B7-1、CD28、细胞毒性 T 淋巴细胞相关蛋白 4(CTLA4)。三组间尿 TNF-α(p<0.001)、血清 TNFR1(p<0.001)、血清 TNFR2(p<0.001)、CTLA4(p<0.001)和 CD28(p=0.034)浓度存在显著差异。多元分析显示,与 ACR 相关的独立参数为血清 TNFR1(p=0.003)、TNFR2(p=0.012)和尿 TNF-α(p=0.015)水平。T 细胞活化标志物与 TNF-α 信号通路活化之间存在显著相关性。TNF-α 信号通路和 T 淋巴细胞的活化似乎协同作用并参与 2 型糖尿病患者 DN 的发生发展。