Department of Internal Medicine, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Department of Immunology, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
Lupus. 2020 Apr;29(4):379-388. doi: 10.1177/0961203320904997. Epub 2020 Feb 10.
TNF-like weak inducer of apoptosis (TWEAK), monocyte chemoattractant protein-1 (MCP-1) and neutrophil gelatinase-associated lipocalin (NGAL) are proinflammatory cytokines/chemokines that are considered as potential biomarkers reflecting disease activity in systemic lupus erythematosus (SLE). In this study, we aimed to investigate the association of serum (s) and urine (u) levels of TWEAK, MCP-1 and NGAL with disease activity in both renal and extra-renal SLE.
Thirty active patients with SLE (15 renal and 15 extra-renal) were recruited. Thirty-one inactive patients with SLE (16 renal and 15 extra-renal), 14 patients with ANCA-associated vasculitis (AAV) all of whom had active renal involvement and 20 healthy volunteers were selected as control groups. Serum and urine levels of TWEAK, MCP-1 and NGAL were tested using ELISA.
Serum and urine levels of TWEAK and NGAL were significantly higher in the active SLE group compared to the inactive SLE group (sTWEAK = 0.005; uTWEAK = 0.026; sNGAL < 0.001; uNGAL = 0.002), whilst no significant differences regarding serum and urine MCP-1 levels were observed ( = 0.189 and = 0.106, respectively). uTWEAK ( = 0.237), sMCP-1 ( = 0.141), uMCP-1 ( = 0.206), sNGAL ( = 0.419) and uNGAL ( = 0.443) levels did not differ between patients with active renal and extra-renal SLE. Serum TWEAK was higher in patients with active renal SLE ( = 0.006). There were no differences between active renal SLE and active renal AAV. Levels of all biomarkers were correlated with the SLE Disease Activity Index.
sTWEAK, uTWEAK, sNGAL and uNGAL are biomarkers showing disease activity in SLE. However, our results implicate that these biomarkers may not be specific for SLE, and can be elevated in patients with active renal involvement of AAV.
TNF 样凋亡弱诱导因子(TWEAK)、单核细胞趋化蛋白-1(MCP-1)和中性粒细胞明胶酶相关脂质运载蛋白(NGAL)是促炎细胞因子/趋化因子,被认为是反映系统性红斑狼疮(SLE)疾病活动的潜在生物标志物。在这项研究中,我们旨在探讨血清(s)和尿液(u)中 TWEAK、MCP-1 和 NGAL 水平与肾脏和肾脏外 SLE 疾病活动的关系。
招募了 30 名活动性 SLE 患者(15 名肾脏受累和 15 名肾脏外受累)。选择 31 名非活动性 SLE 患者(16 名肾脏受累和 15 名肾脏外受累)、14 名抗中性粒细胞胞质抗体相关血管炎(AAV)患者(均有活动期肾脏受累)和 20 名健康志愿者作为对照组。使用 ELISA 检测 TWEAK、MCP-1 和 NGAL 的血清和尿液水平。
与非活动性 SLE 组相比,活动性 SLE 组的血清和尿液 TWEAK 和 NGAL 水平显著升高(sTWEAK=0.005;uTWEAK=0.026;sNGAL<0.001;uNGAL=0.002),而血清和尿液 MCP-1 水平无显著差异(=0.189 和=0.106)。uTWEAK(=0.237)、sMCP-1(=0.141)、uMCP-1(=0.206)、sNGAL(=0.419)和 uNGAL(=0.443)水平在活动性肾脏和肾脏外 SLE 患者之间无差异。sTWEAK 在活动性肾脏 SLE 患者中较高(=0.006)。活动性肾脏 SLE 与活动性肾脏 AAV 之间无差异。所有生物标志物水平与 SLE 疾病活动指数相关。
sTWEAK、uTWEAK、sNGAL 和 uNGAL 是 SLE 疾病活动的生物标志物。然而,我们的结果表明,这些生物标志物可能不是 SLE 的特异性标志物,并且可能在活动性 AAV 肾脏受累患者中升高。