BK Polyomavirus-associated nephropathy - diagnostic and treatment standard

被引:0
作者
Al-Talib, Mohammed [1 ,2 ]
Welberry-Smith, Matthew [3 ,4 ]
Macdonald, Andrew [3 ]
Griffin, Sian [5 ]
机构
[1] Cardiff Univ, Syst Immun Res Inst, Sch Med, Div Infect & Immun, Cardiff, Wales
[2] Univ Bristol, Bristol Med Sch, 5 Tyndall Ave, Bristol, England
[3] Univ Leeds, Fac Biol Sci, Woodhouse Lane, Leeds, England
[4] Leeds Teaching Hosp NHS Trust, Dept Renal Med & Transplantat, Beckett St, Leeds, England
[5] Cardiff & Vale Univ Hlth Board, Dept Nephrol & Transplantat, Cardiff, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
BK polyomavirus-associated nephropathy; diagnosis; pathophysiology; prognosis; treatment; RENAL-TRANSPLANT RECIPIENTS; KIDNEY-TRANSPLANTATION; VIRUS; REPLICATION; VIREMIA; IMPACT; CYCLOSPORINE; INFECTIONS; TACROLIMUS; IMMUNITY;
D O I
10.1093/ndt/gfaf002
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
BK polyomavirus (BKPyV) is recognized as a significant viral complication of kidney transplantation. Prompt immunosuppression reduction reduces early graft failure rates due to BK polyomavirus-associated nephropathy (BKPyVAN), however, modulation of immunosuppression can lead to acute rejection. Medium-to-long-term graft outcomes are negatively affected by BKPyVAN, probably due to a combination of virus-induced graft damage and host immune responses against graft alloantigens potentiated by immunosuppression reduction. Kidney biopsy remains the gold-standard diagnostic test, however, false-negative findings are common due to the focal nature of BKPyVAN. BKPyV DNAemia, as measured by quantitative polymerase chain reaction, is established as a screening test but there is at present no (inter)national standardization of these assays to allow collation and comparison of data between centres. Randomized controlled trials are lacking both in terms of optimal immunosuppression reduction strategies, and for the medications variably used to attempt treatment in clinical practice. Much of the fundamental biology of BKPyV is not yet understood, and further elucidation is required to promote rational direct-acting antiviral drug design. Insights into the role of adaptive immunity in control of BKPyV have informed the design of novel treatments such as adoptive immunotherapies and neutralizing antibodies that require evaluation in clinical studies. Here, we review the current standards of diagnosis and treatment of BKPyVAN and discuss novel developments in the pathophysiology, diagnosis, outcome prediction, and management.
引用
收藏
页码:651 / 661
页数:11
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