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在异基因干细胞移植后,JC多瘤病毒再激活很常见,其抢先检测可能预防致命并发症。

JC polyomavirus reactivation is common following allogeneic stem cell transplantation and its preemptive detection may prevent lethal complications.

作者信息

Wittmann T, Horowitz N, Benyamini N, Henig I, Zuckerman T, Rowe J M, Kra-Oz Z, Szwarcwort Cohen M, Oren I, Avivi I

机构信息

Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel.

1] Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel [2] Department of Hematology and Bone Marrow Transplantation, Rambam Health Care Campus, Haifa, Israel.

出版信息

Bone Marrow Transplant. 2015 Jul;50(7):984-91. doi: 10.1038/bmt.2015.68. Epub 2015 Apr 13.

Abstract

Extended application of allogeneic stem cell transplantation (alloSCT) is expected to increase the frequency of JC polyomavirus (JCPyV)-related progressive multifocal leukoencephalopathy (PML). The aim of this study was to assess frequency, risk factors and course of JCPyV reactivation in allografted hematology patients. This retrospective study included consecutive adult patients, treated with alloSCT between January 2008 and December 2011. Quantitative JCPyV-PCR analysis was performed on whole blood DNA samples, originally drawn for cytomegalovirus detection since transplant date. The study included 164 patients diagnosed with hematological malignancies. Patients received reduced-intensity conditioning (n=74) or myeloablative conditioning (n=90), followed by alloSCT. Twenty patients developed transient and 20 had persistent JCPyV reactivation. Two of the patients with persistent reactivation showed a gradual increase in JCPyV levels, preceding PML development by 96 and 127 days. Cessation of immunosuppression resulted in complete resolution of neurological symptoms in one patient, while the other died of PML. Seventy percent of the 'persistently reactivating' patients died. Multivariate analysis confirmed age to be the only significant predictive factor for JCPyV reactivation. In conclusion, JCPyV reactivation occurs in a quarter of allografted patients. Preemptive detection of JCPyV reactivation in high-risk subjects and early discontinuation of immunosuppressive therapy may prevent development of lethal PML.

摘要

异体干细胞移植(alloSCT)的广泛应用预计会增加与JC多瘤病毒(JCPyV)相关的进行性多灶性白质脑病(PML)的发生率。本研究的目的是评估接受同种异体移植的血液学患者中JCPyV再激活的发生率、危险因素及病程。这项回顾性研究纳入了2008年1月至2011年12月期间接受alloSCT治疗的成年连续患者。对自移植之日起最初为检测巨细胞病毒而采集的全血DNA样本进行JCPyV定量PCR分析。该研究纳入了164例被诊断为血液系统恶性肿瘤的患者。患者接受了减低强度预处理(n = 74)或清髓性预处理(n = 90),随后进行alloSCT。20例患者出现短暂性JCPyV再激活,20例出现持续性JCPyV再激活。两名持续性再激活患者的JCPyV水平逐渐升高,在发生PML前96天和127天。停用免疫抑制治疗后,一名患者的神经症状完全缓解,而另一名患者死于PML。70%的“持续性再激活”患者死亡。多变量分析证实年龄是JCPyV再激活的唯一显著预测因素。总之,JCPyV再激活发生在四分之一的同种异体移植患者中。对高危受试者进行JCPyV再激活的抢先检测并早期停用免疫抑制治疗可能预防致命性PML的发生。

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