Department of Translational Medicine, Section of Medical Protein Chemistry, Lund University, Malmö, Sweden.
Region Skåne, Laboratory Medicine, Clinical Chemistry, Malmö, Sweden.
Front Immunol. 2020 Oct 2;11:582737. doi: 10.3389/fimmu.2020.582737. eCollection 2020.
To examine whether C4d plasma levels correlate with treatment response and C4d kidney deposition in systemic lupus erythematosus (SLE) with lupus nephritis (LN).
C4d plasma levels were analyzed by a unique assay specifically detecting C4d arising from complement activation and C4 plasma levels were quantified with competitive ELISA. SLE patients with LN (71) and active SLE patients without LN (22) plus 145 controls were included. For 52 LN patients samples were available both at baseline and after immunosuppressive treatment. C4d kidney deposition was detected using immunohistochemistry in two matching kidney biopsies of 12 LN patients.
In comparison to population-based controls, plasma C4d levels were significantly increased in SLE patients (0.33 mg/L versus 0.94 mg/ml, < 0.0001) with significantly higher levels in LN patients (1.02 mg/L) than in non-renal SLE patients (0.57 mg/L, = 0.004). The C4d/C4 ratio was also significantly higher in LN (11.2) than in non-renal SLE patients (2.5, = 0.0002). According to ROC curve analysis, C4d was found to be an accurate marker to discriminate LN from non-renal SLE patients ( = 0.004). The C4d/C4 ratio displayed even higher specificity, sensitivity and overall accuracy as marker for LN than C4d and C4 alone. At baseline, C4d levels correlated significantly with urine-albumin to creatinine ratio ( = 0.43, = 0.011) and with renal activity index ( = 0.37, = 0.002). Immunohistochemical staining showed glomerular deposits of C4d in kidney biopsies, which strikingly correlated with plasma C4d levels ( = 0.7, = 0.0002). Plasma C4d declined significantly after treatment in patients that experienced favorable clinical and histopathological response ( < 0.0001), while levels remained mainly unchanged in non-responders.
Plasma C4d discriminates LN from active non-renal SLE, correlates with C4d kidney deposits and appears valuable in monitoring responsiveness to various treatments. The C4d/C4 ratio might be superior to C4d alone.
探讨补体因子 D(C4d)在系统性红斑狼疮(SLE)合并狼疮性肾炎(LN)患者血浆中的水平是否与治疗反应及 C4d 肾脏沉积相关。
采用一种独特的检测方法分析 C4d 血浆水平,该方法特异性检测补体激活产生的 C4d,同时采用竞争 ELISA 定量检测 C4 血浆水平。纳入 71 例 LN 患者、22 例活动期非 LN 系统性红斑狼疮(SLE)患者及 145 例对照者。52 例 LN 患者在基线和免疫抑制治疗后均有样本。采用免疫组化方法在 12 例 LN 患者的 2 对匹配的肾活检标本中检测 C4d 肾脏沉积。
与基于人群的对照组相比,SLE 患者的血浆 C4d 水平明显升高(0.33mg/L 比 0.94mg/ml,<0.0001),LN 患者(1.02mg/L)高于非肾脏 SLE 患者(0.57mg/L,=0.004)。LN 患者的 C4d/C4 比值也明显高于非肾脏 SLE 患者(11.2 比 2.5,=0.0002)。根据 ROC 曲线分析,C4d 是区分 LN 与非肾脏 SLE 患者的准确标志物(=0.004)。C4d/C4 比值作为 LN 的标志物比 C4d 和 C4 本身具有更高的特异性、敏感性和总体准确性。在基线时,C4d 水平与尿白蛋白/肌酐比值(=0.43,=0.011)和肾脏活动指数(=0.37,=0.002)显著相关。免疫组化染色显示肾活检中 C4d 的肾小球沉积,与血浆 C4d 水平呈显著相关(=0.7,=0.0002)。在经历了有利的临床和组织病理学反应的患者中,C4d 水平在治疗后显著下降(<0.0001),而在无反应者中水平基本保持不变。
血浆 C4d 可区分 LN 与活动期非肾脏 SLE,与 C4d 肾脏沉积相关,在监测对各种治疗的反应方面可能具有价值。C4d/C4 比值可能优于单独的 C4d。