Dynamics of BKPyV reactivation and risk of hemorrhagic cystitis after allogeneic hematopoietic stem cell transplantation

被引:7
作者
Hoeller, Konstantin [1 ]
Fabeni, Lavinia [2 ]
Herling, Marco [3 ,4 ]
Holtick, Udo [3 ,4 ]
Scheid, Christof [3 ,4 ]
Knops, Elena [1 ]
Luebke, Nadine [1 ]
Kaiser, Rolf [1 ]
Pfister, Herbert [1 ]
Di Cristanziano, Veronica [1 ]
机构
[1] Univ Cologne, Inst Virol, Cologne, Germany
[2] Natl Inst Infect Dis L Spallanzani IRCCS, Rome, Italy
[3] Univ Hosp Cologne, Dept Internal Med 1, Ctr Integrated Oncol CIO Koln Bonn, Cologne, Germany
[4] Univ Hosp Cologne, Excellence Cluster Cellular Stress Response & Agi, Cologne, Germany
关键词
BKPyV; BKPyV subtype; hematopoietic stem cell transplantation; hemorrhagic cystitis; immunosuppression; latent infection; polyomavirus; viral reactivation; BK VIRUS-INFECTION; POLYOMAVIRUS BK; NEPHROPATHY; RECIPIENTS; IDENTIFICATION; ASSOCIATION; PREVALENCE; VIREMIA; PLASMA; URINE;
D O I
10.1111/ejh.12895
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectivesAim of this retrospective study was to analyze the dynamics of BKPyV reactivation in allogeneic hematopoietic stem cell transplant recipients in order to identify patients with higher risk to develop BKPyV-associated hemorrhagic cystitis (BKPyV-associated HC). MethodsThe study included 58 allo-HSCT recipients from the University Hospital of Cologne detected BKPyV positive by real-time PCR between 2009 and 2015. For correlative analysis, the first detected BKPyV-DNA load in urine and in plasma as well as the onset and severity of HC following the first day of conditioning regimen was considered. Phylogenetic analysis of BKPyV isolates was performed. ResultsIn 25 of 58 patients, BKPyV-DNA was detected in urine only (group U), whereas 33 patients developed additional viremia (group P). A chronologic sequence viruria-viremia-HC was identified. Viral load of >10(6) copies/mL at first viruria and evidence of viremia after 45days from the start of conditioning represented risk factors for the onset of HC. Molecular characterization revealed a non-stereotypic distribution of viral subtypes across groups U and P. ConclusionsMonitoring of BKPyV-DNA by real-time PCR after initiation of conditioning, regularly performed in clinical practice, can be a crucial tool for the early identification of patients with higher risk of BKPyV-associated HC.
引用
收藏
页码:133 / 140
页数:8
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