Gupta Ranjan, Yadav Akhilesh, Aggarwal Amita
Department of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, 226014, India.
Department of Rheumatology, All India Institute of Medical Sciences, New Delhi, India.
Clin Rheumatol. 2021 Mar;40(3):941-948. doi: 10.1007/s10067-020-05343-6. Epub 2020 Aug 18.
Activated macrophages expressing CD163 (M2) are the most abundant macrophage subtype in renal biopsies from lupus nephritis (LN) patients. We studied the role of proteolytically cleaved soluble CD163 (sCD163) as a biomarker of LN disease activity.
SLE patients were classified as active LN (AN), inactive disease (ID), and active non-renal disease (ANR). Urine and plasma samples were collected at baseline from all patients and at 3 monthly follow-up from AN patients. sCD163 was measured by ELISA. Urine values were normalized to urinary creatinine excretion and expressed as pg/mg. Urine samples from 25 healthy controls (HC) and 20 rheumatoid arthritis patients served as disease controls (DC).
Among the 122 patients studied (114 females, 57 AN, 42 ID, 23 ANR), baseline median urinary sCD163 in the AN group (114.01 pg/mg) was significantly higher (p < 0.001) as compared with ID (10.34 pg/mg), ANR (3.82 pg/mg), HC (0 pg/mg), and DC (7.56 pg/mg) groups and showed modest correlation with renal SLEDAI (r = 0.47; p < 0.001). Urinary sCD163 performed the best on receiver operating characteristics (ROC) analysis (AUC = 0.76) at baseline to differentiate between AN and ANR as compared with plasma sCD163, anti-ds DNA antibodies, and C3 and C4. In follow-up study, urinary sCD163 decreased significantly (p < 0.001) in AN patients at 3 (22.07 pg/mg), 6 (12.7 pg/mg), 9 (11.09 pg/mg), and 12 months (7.2 pg/mg). In 4 patients who had either relapse or developed CKD, urinary sCD163 levels correlated with the changing disease activity.
Urinary sCD163 is a good biomarker of LN disease activity. Key Points • Urinary sCD163 levels are raised in patients with active lupus nephritis and correlate with renal SLEDAI. • Urinary sCD163 levels fall after treatment and may be helpful in monitoring response to therapy in lupus nephritis.
表达CD163的活化巨噬细胞(M2)是狼疮性肾炎(LN)患者肾活检中最丰富的巨噬细胞亚型。我们研究了蛋白水解裂解的可溶性CD163(sCD163)作为LN疾病活动生物标志物的作用。
将SLE患者分为活动性LN(AN)、非活动性疾病(ID)和活动性非肾脏疾病(ANR)。在基线时从所有患者收集尿液和血浆样本,并在AN患者随访3个月时收集样本。通过ELISA检测sCD163。将尿液值标准化为尿肌酐排泄量,并以pg/mg表示。来自25名健康对照(HC)和20名类风湿性关节炎患者的尿液样本用作疾病对照(DC)。
在研究的122例患者中(114例女性,57例AN,42例ID,23例ANR),AN组的基线尿sCD163中位数(114.01 pg/mg)与ID组(10.34 pg/mg)、ANR组(3.82 pg/mg)、HC组(0 pg/mg)和DC组(7.56 pg/mg)相比显著更高(p < 0.001),并且与肾脏SLEDAI呈适度相关(r = 0.47;p < 0.001)。在基线时,与血浆sCD163、抗双链DNA抗体、C3和C4相比,尿sCD163在区分AN和ANR的受试者工作特征(ROC)分析中表现最佳(AUC = 0.76)。在随访研究中,AN患者在3个月(22.07 pg/mg)、6个月(12.7 pg/mg)、9个月(11.09 pg/mg)和12个月(7.2 pg/mg)时尿sCD163显著下降(p < 0.001)。在4例复发或发展为CKD的患者中,尿sCD163水平与疾病活动变化相关。
尿sCD163是LN疾病活动的良好生物标志物。要点:•活动性狼疮性肾炎患者尿sCD163水平升高,且与肾脏SLEDAI相关。•治疗后尿sCD163水平下降,可能有助于监测狼疮性肾炎的治疗反应。