Human herpesvirus 6 can be detected in cerebrospinal fluid without associated symptoms after allogeneic hematopoietic cell transplantation

被引:29
作者
Hill, Joshua A. [1 ,2 ]
Boeckh, Michael J. [1 ,2 ]
Sedlak, Ruth Hall [3 ]
Jerome, Keith R. [2 ,3 ]
Zerr, Danielle M. [2 ,4 ]
机构
[1] Univ Washington, Div Allergy & Infect Dis, Seattle, WA 98195 USA
[2] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98109 USA
[3] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[4] Seattle Childrens Res Inst, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
Herpesvirus; hhv-6; Transplant; Encephalitis; CNS; Neurologic; ACUTE LIMBIC ENCEPHALITIS; CLINICAL-FEATURES;
D O I
10.1016/j.jcv.2014.07.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Human herpesvirus 6 (HHV-6) is an opportunistic pathogen after hematopoietic cell transplantation (HCT) that is associated with central nervous system (CNS) dysfunction. Objectives: The aim of this study was to determine the frequency and significance of HHV-6 DNA detection in cerebrospinal fluid (CSF) after HCT. Study design: We identified patients with HHV-6 DNA in CSF using quantitative PCR. Patients with neurologic symptoms and HHV-6 DNA in CSF without identification of an alternative etiology were categorized as having HHV-6 CNS dysfunction. Results: Among 3902 allogeneic HCT recipients from 1998 to 2012,51 of 124 tested patients had HHV-6 DNA in CSF; 37 met criteria for HHV-6 CNS dysfunction and 14(27%) did not. Patients with an alternative diagnosis had longer time to HHV-6 detection and lower viral load in CSF. Six patients without HHV-6 CNS dysfunction were not treated and had no morbidity attributable to HHV-6. Kaplan-Meier analysis demonstrated poor overall survival among all patients. Variables associated with higher all-cause mortality in a multivariable Cox model included alternative diagnosis (adjusted hazard ratio [aHR], 8.4; 95% CI, 1.7-40.9; P =0.009) and higher peak plasma viral load (logio scale) (aHR, 1.4; 95% CI, 1.1-1.9; P = 0.01). Conclusion: We identified a number of allogeneic HCT recipients with HHV-6 DNA in CSF who did not meet criteria for HHV-6 CNS dysfunction. All patients had poor survival. Whether CSF HHV-6 DNA detection in patients without associated CNS dysfunction independently contributes to mortality and warrants treatment is unclear; management of these patients warrants further investigation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:289 / 292
页数:4
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