BK Polyomavirus in Pediatric Renal Transplantation-What We Know and What We Do Not

被引:0
作者
Chiodini, Benedetta [1 ]
Guillaume-Gentil, Pauline [1 ]
Vanhomwegen, Charlotte [2 ]
Hennaut, Elise [1 ]
Lolin, Ksenija [1 ]
Tram, Nathalie [1 ]
Le Moine, Alain [2 ]
Ismaili, Khalid [1 ]
机构
[1] Univ Libre Bruxelles ULB, Hop Univ Bruxelles HUDERF, Dept Pediat Nephrol, B-1050 Brussels, Belgium
[2] Univ Libre Bruxelles ULB, Hop Univ Bruxelles HUB, Dept Radiat Oncol, B-1070 Brussels, Belgium
关键词
BK polyomavirus; BKPyV nephropathy; kidney transplantation; VIRUS ALLOGRAFT NEPHROPATHY; POLYMERASE-CHAIN-REACTION; INTRAVENOUS IMMUNOGLOBULIN; LEFLUNOMIDE THERAPY; IMMUNE-RESPONSES; JC VIRUS; KIDNEY; RECIPIENTS; REPLICATION; VIREMIA;
D O I
10.3390/biomedicines12051093
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BK polyomavirus (BKPyV) is still a real threat in the management of kidney transplantation. Immunosuppressive treatment disrupts the equilibrium between virus replication and immune response, and uncontrolled BKPyV replication leads to nephropathy (BKPyV nephropathy). The first evidence of BKPyV reactivation in transplant recipients is the detection of viral shedding in urine, which appears in 20% to 60% of patients, followed by BKPyV viremia in 10-20% of kidney transplant recipients. BKPyV nephropathy eventually occurs in 1-10% of this population, mainly within the first 2 years post-transplantation, causing graft loss in about half of those patients. Few data exist regarding the pediatric population and we focus on them. In this paper, we review the existing diagnostic methods and summarize the evidence on the role of BKPyV humoral and cellular immunity in modulating the clinical course of BKPyV infection and as potential predictors of the outcome. We look at the known risk factors for BKPyV nephropathy in the immunosuppressed patient. Finally, we propose a sensible clinical attitude in order to screen and manage BKPyV infection in kidney transplant children.
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页数:11
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