Santoro Jonathan D, Hemond Christopher C
Division of Child Neurology, Department of Neurology, Stanford University School of Medicine, Palo Alto, California.
Department of Neurology, University of Massachusetts Medical Center, Worcester, Massachusetts.
Transpl Infect Dis. 2019 Feb;21(1):e13003. doi: 10.1111/tid.13003. Epub 2018 Oct 15.
Human herpesvirus 6 (HHV6) is a cause of post-transplant acute limbic encephalitis (PALE). Seizures are associated with this disorder yet no predictive biomarkers have been identified. The objective of this study was to evaluate lab and neurodiagnostic biomarkers in patients with HHV6 associated PALE.
A retrospective chart review was performed at our institutions between 2000 and 2017. Patients were identified through a clinical database. Inclusion criteria included: age less than 18 years, HHV6 (quantitative real-time PCR or meningoencephalitis panel) tested in CSF and serum. Biomarkers of serum and CSF viral load, EEG, and MRI were reviewed along with clinical data.
In total, 11 patients met inclusion criteria. All patients had undergone hematopoietic stem cell transplantation. Five of 11 patients had seizures as part of their clinical course, all being controlled with antiepileptic monotherapy. Seizure semiology was focal-onset in three cases and generalized in two. Neuroimaging was normal in all patients within seven days but six patients developed T2 signal intensities in the temporal lobes on repeat imaging between 14-28 days. The median CSF HHV6 viral load for all patients was 47 300 copies/mL although the median viral load was 2586 copies/mL in patients who had seizure compared to 473 969 copies/mL in those who had not (P = 0.02). Those with seizures tended to be younger (median 6.5 years compared to 11 years, P = 0.27). All patients with seizures had an EEG with 80% demonstrating abnormalities.
In patients with post-hematopoietic stem cell transplant HHV6 associated PALE, lower CSF viral load may be associated with a higher likelihood to have seizures. This may indicate a primary infection as opposed to secondary reactivation phenomenon.
人类疱疹病毒6型(HHV6)是移植后急性边缘叶脑炎(PALE)的病因。癫痫发作与该疾病相关,但尚未确定预测性生物标志物。本研究的目的是评估HHV6相关PALE患者的实验室和神经诊断生物标志物。
2000年至2017年在我们机构进行了一项回顾性病历审查。通过临床数据库识别患者。纳入标准包括:年龄小于18岁,脑脊液和血清中检测到HHV6(定量实时PCR或脑膜脑炎检测组)。审查了血清和脑脊液病毒载量、脑电图和磁共振成像的生物标志物以及临床数据。
共有11名患者符合纳入标准。所有患者均接受了造血干细胞移植。11名患者中有5名在临床过程中出现癫痫发作,均通过抗癫痫单药治疗得到控制。癫痫发作的症状学在3例中为局灶性发作,2例为全身性发作。所有患者在7天内神经影像学检查均正常,但6例患者在14 - 28天的重复成像中颞叶出现T2信号强度。所有患者脑脊液中HHV6病毒载量的中位数为47300拷贝/mL,尽管癫痫发作患者的病毒载量中位数为2586拷贝/mL,未发作患者为473969拷贝/mL(P = 0.02)。癫痫发作患者往往更年轻(中位数为6.5岁,而未发作患者为11岁,P = 0.27)。所有癫痫发作患者的脑电图检查中80%显示异常。
在造血干细胞移植后HHV6相关PALE患者中,脑脊液病毒载量较低可能与癫痫发作的可能性较高有关。这可能表明是原发性感染而非继发性再激活现象。