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
收藏
页数:13
相关论文
共 43 条
[1]   BK Polyomavirus Virus Glomerular Tropism: Implications for Virus Reactivation from Latency and Amplification during Immunosuppression [J].
Alcendor, Donald J. .
JOURNAL OF CLINICAL MEDICINE, 2019, 8 (09)
[2]   Simultaneous immunostaining with anti-S100P and anti-SV40 antibodies revealed the origin of BK virus-infected decoy cells in voided urine samples [J].
Ariyasu, S. ;
Yanai, H. ;
Sato, M. ;
Shinno, Y. ;
Taniguchi, K. ;
Yamadori, I. ;
Miki, Y. ;
Sato, Y. ;
Yoshino, T. ;
Takahashi, K. .
CYTOPATHOLOGY, 2015, 26 (04) :250-255
[3]   Sustained BK Viruria as an Early Marker for the Development of BKV-Associated Nephropathy: Analysis of 4128 Urine and Serum Samples [J].
Babel, Nina ;
Fendt, Juliane ;
Karaivanov, Stoyan ;
Bold, Gantuja ;
Arnold, Steffen ;
Sefrin, Anett ;
Lieske, Evelyn ;
Hoffzimmer, Martin ;
Dziubianau, Mikalai ;
Bethke, Nicole ;
Meisel, Christian ;
Gruetz, Gerald ;
Reinke, Petra .
TRANSPLANTATION, 2009, 88 (01) :89-95
[4]   Quantification of BK Virus Standards by Quantitative Real-Time PCR and Droplet Digital PCR Is Confounded by Multiple Virus Populations in the WHO BKV International Standard [J].
Bateman, Allen C. ;
Greninger, Alexander L. ;
Atienza, Ederlyn E. ;
Limaye, Ajit P. ;
Jerome, Keith R. ;
Cook, Linda .
CLINICAL CHEMISTRY, 2017, 63 (03) :761-769
[5]   Advances in Urine Microscopy [J].
Becker, Gavin J. ;
Garigali, Giuseppe ;
Fogazzi, Giovanni B. .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2016, 67 (06) :954-964
[6]  
Brennan DC., American Journal of Transplantation
[7]   A prospective longitudinal study of BK virus infection in 104 renal transplant recipients [J].
Bressollette-Bodin, C ;
Coste-Burel, M ;
Hourmant, M ;
Sebille, V ;
Andre-Garnier, E ;
Imbert-Marcille, BM .
AMERICAN JOURNAL OF TRANSPLANTATION, 2005, 5 (08) :1926-1933
[8]   Glomerular changes in BK virus nephropathy [J].
Celik, B ;
Randhawa, PS .
HUMAN PATHOLOGY, 2004, 35 (03) :367-370
[9]   Glomerular Parietal Epithelial Cells Infection Is Associated With Poor Graft Outcome in Kidney Transplant Recipients With BK Polyomavirus-Associated Nephropathy [J].
Chen, Xu-Tao ;
Yang, Shi-Cong ;
Chen, Wen-Fang ;
Li, Jun ;
Deng, Su-Xiong ;
Qiu, Jiang ;
Fei, Ji-Guang ;
Deng, Rong-Hai ;
Chen, Yan-Yang ;
Chen, Pei-Song ;
Huang, Yang ;
Wang, Chang-Xi ;
Huang, Gang .
JOURNAL OF INFECTIOUS DISEASES, 2019, 219 (12) :1879-1886
[10]   Immunohistochemical differentiation of high-grade prostate carcinoma from urothelial carcinoma [J].
Chuang, Ai-Ying ;
DeMarzo, Angelo M. ;
Veltri, Robert W. ;
Sharma, Rajni B. ;
Bieberich, Charles J. ;
Epstein, Jonathan I. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2007, 31 (08) :1246-1255