Crawford John R, Santi Maria R, Thorarinsdottir Halldora K, Cornelison Robert, Rushing Elisabeth J, Zhang Huizhen, Yao Karen, Jacobson Steven, Macdonald Tobey J
The Department of Neurology, Children's National Medical Center, The George Washington University, Washington, DC, United States.
J Clin Virol. 2009 Sep;46(1):37-42. doi: 10.1016/j.jcv.2009.05.011. Epub 2009 Jun 7.
Human herpesvirus-6 (HHV-6) has been associated with a diverse spectrum of central nervous system (CNS) diseases and reported glial tropism.
To determine if HHV-6 is present in a series of pediatric brain tumors.
Pediatric gliomas from 88 untreated patients represented in a tissue microarray (TMA) were screened for HHV-6 by nested polymerase chain reaction (PCR), in situ hybridization (ISH), and immunohistochemistry (IHC) and compared to non-glial tumors (N=22) and control brain (N=32). Results were correlated with tumor grade and overall survival.
HHV-6 U57 was detected by nested PCR in 68/120 (57%) tumors and 7/32 (22%) age-matched non-tumor brain (P=0.001). HHV-6 U31 was positive in 73/120 (61%) tumors and 11/32 (34%) controls (P=0.019). Seventy-two percent (43/60) of tumors were HHV-6 Variant A. HHV-6 U57 was confirmed by ISH in 83/150 (54%) tumors and 10/32 (31%) controls (P=0.021), revealing a non-lymphocytic origin of HHV-6. HHV-6A/B gp116/64/54 late antigen was detected by IHC in 50/124 (40%) tumors and 6/32 (18%) controls (P=0.013). Interestingly, 58% of low grade gliomas (N=67) were IHC positive compared to 19% of high grade gliomas (N=21, P=0.002) and 25% of non-gliomas (N=36, P=0.001). HHV-6A/B gp116/64/54 antigen co-localized with glial fibrillary acidic protein, confirming the astrocytic origin of antigen. Overall, there was no primary association between HHV-6A/B gp116/64/54 antigen detection and survival (P=0.861).
We provide the first reported series of HHV-6 detection in pediatric brain tumors. The predominance of HHV-6 in glial tumors warrants further investigation into potential neurooncologic disease mechanisms.
人类疱疹病毒6型(HHV-6)与多种中枢神经系统(CNS)疾病相关,并报道具有嗜神经胶质细胞特性。
确定HHV-6是否存在于一系列小儿脑肿瘤中。
通过巢式聚合酶链反应(PCR)、原位杂交(ISH)和免疫组织化学(IHC)对组织芯片(TMA)中88例未经治疗患者的小儿胶质瘤进行HHV-6筛查,并与非神经胶质细胞瘤(N = 22)和对照脑(N = 32)进行比较。结果与肿瘤分级和总生存期相关。
通过巢式PCR在68/120(57%)的肿瘤和7/32(22%)年龄匹配的非肿瘤脑中检测到HHV-6 U57(P = 0.001)。HHV-6 U31在73/120(61%)的肿瘤和11/32(34%)的对照中呈阳性(P = 0.019)。72%(43/60)的肿瘤为HHV-6 A变异株。通过ISH在83/150(54%)的肿瘤和10/32(31%)的对照中证实了HHV-6 U57(P = 0.021),揭示了HHV-6的非淋巴细胞起源。通过IHC在50/124(40%)的肿瘤和6/32(18%)的对照中检测到HHV-6A/B gp116/64/54晚期抗原(P = 0.013)。有趣的是,58%的低级别胶质瘤(N = 67)IHC呈阳性,而高级别胶质瘤为19%(N = 21,P = 0.002),非神经胶质细胞瘤为25%(N = 36,P = 0.001)。HHV-6A/B gp116/64/54抗原与胶质纤维酸性蛋白共定位,证实了抗原的星形细胞起源。总体而言,HHV-6A/B gp116/64/54抗原检测与生存期之间无主要关联(P = 0.861)。
我们提供了首次报道的小儿脑肿瘤中HHV-6检测系列。HHV-6在神经胶质细胞瘤中的优势地位值得进一步研究潜在神经肿瘤疾病机制。