Non-invasive urinary sediment double-immunostaining predicts BK polyomavirus associated-nephropathy in kidney transplant recipients

被引:8
作者
Chen, Xu-Tao [1 ]
Chen, Wen-Fang [2 ]
Hou, Xiao-Tao [3 ]
Yang, Shi-Cong [2 ]
Yang, Hui-Fei [4 ]
Li, Jun [1 ]
Deng, Rong-Hai [1 ]
Huang, Yang [1 ]
Nuertai, Yelidana [5 ]
Wang, Chang-Xi [1 ]
Qiu, Jiang [1 ]
Huang, Gang [1 ]
机构
[1] Sun Yat Sen Univ, Dept Organ Transplantat, Affiliated Hosp 1, Guangzhou 510080, Peoples R China
[2] Sun Yat Sen Univ, Dept Pathol, Affiliated Hosp 1, Guangzhou 510080, Peoples R China
[3] Guangzhou KingMed Ctr Clin Lab Co Ltd, Guangzhou Int Biotech Isl, Guangzhou 510005, Peoples R China
[4] Jinan Univ, Fuda Canc Hosp, Guangzhou 510640, Peoples R China
[5] Sun Yat Sen Univ, Zhongshan Sch Med, Guangzhou 510080, Peoples R China
基金
中国国家自然科学基金;
关键词
BK polyomavirus; BKPyVAN; decoy cells; double-immunostaining; kidney transplantation; REAL-TIME PCR; ACCURATELY PREDICTS; VIRUS; IMMUNOSUPPRESSION; REPLICATION; MARKER; DIFFERENTIATION; REDUCTION; CARCINOMA; VIREMIA;
D O I
10.21037/atm.2020.01.15
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The positive predictive value (PPV) of urinary decoy cells for diagnosing BK polyomavirus associated-nephropathy (BKPyVAN) is low. This study was designed to increase the PPV of urinary decoy cells for diagnosing BKPyVAN in kidney transplant recipients. Methods: A total of 105 urine sediment samples from 105 patients with positive BK viruria and decoy cells were evaluated by automatic double-immunostaining with anti-HGD (a renal tubular marker) antibody + anti-SV40-T antibody or anti-SlOOP (an urothelial marker) antibody + anti-SV40-T antibody. Results: Of the 105 patients, 76 (72.4%) had both HGD(+)/SV40-T(+) cells and S 100P(+)/SV40-T(+) cells (group A), 24 (22.9%) had only SIOOP(+)/SV40-T(+) cells (group B), and 5 (4.6%) had only S100P(-)/ HGD(-)/SV40-T(+) cells (group C). Seventy patients in group A (92.1%), 3 patients in group B (12.5%), and no patients in group C were diagnosed with BKPyVAN. The area under the ROC curve of predicting BKPyVAN by decoy cells was 0.531 (0.431-0.630), with an optimal cut-off value of 29 (per 10 high power field), a sensitivity of 45.8% (95% CI: 34.0-58.0%), and a specificity of 68.8% (95% CI: 50.0-83.9%). Besides, the area under the ROC curve of predicting BKPyVAN by plasma BKPyV load was 0.735 (95% CI: 0.632-0.822), with an optimal cut-off value of 1,000 copies/mL a sensitivity of 61.1% (95% CI: 48.9-72.4%) and a specificity of 84.2% (95% CI: 60.4-96.6%). In contrast, the PPV, negative predictive value, sensitivity, and specificity of HGD(+)/SV40-T(+) cells for diagnosing BKPyVAN were 92.1% [95% confidence interval (CI): 83.0-96.7%], 89.7% (95% CI: 71.5-97.3%), 95.9% (95% CI: 87.7-98.9%), and 81.3% (95% CI: 63.0-92.1%) respectively. Conclusions: Double-immunostaining with anti-HGD or anti-S1OOP and anti-SV40-T antibodies helps to identify the origin of decoy cells and diagnose BKPyVAN.
引用
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页数:13
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