Fan H, Gulley M L
Department of Pathology, University of Texas Health Science Center, Sun Antonio, TX.
Methods Mol Med. 2001;49:301-11. doi: 10.1385/1-59259-081-0:301.
In situ hybridization (ISH) to Epstein-Barr virus (EBV)-encoded RNA (EBER) is considered the "gold standard" for detecting and localizing latent EBV in biopsy samples. Transcripts from the EBER1 and EBER2 genes are an appropriate target because they are the most abundant viral RNA in latently infected cells, exceeding 1 million transcripts per cell. Furthermore, EBERs are consistently expressed in virtually all EB V-infected tumors and in the lymphoid tissues of infectious mononucleosis (1-5). As a result, EBERs represent a naturally amplified target for detecting and localizing latent EBV in histologic samples. The only EBV-related disorder in which EBER is consistently absent is oral hairy leukoplakia, an infection of squamous epithelial cells in which the virus undergoes lytic viral replication rather than latent infection (6).
针对爱泼斯坦-巴尔病毒(EBV)编码RNA(EBER)的原位杂交(ISH)被认为是检测和定位活检样本中潜伏EBV的“金标准”。EBER1和EBER2基因的转录本是合适的靶标,因为它们是潜伏感染细胞中最丰富的病毒RNA,每个细胞超过100万个转录本。此外,EBERs在几乎所有EBV感染的肿瘤以及传染性单核细胞增多症的淋巴组织中持续表达(1-5)。因此,EBERs是检测和定位组织学样本中潜伏EBV的天然扩增靶标。EBER始终不存在的唯一EBV相关疾病是口腔毛状白斑病,这是一种鳞状上皮细胞感染,其中病毒进行裂解性病毒复制而非潜伏感染(6)。