Ambinder R F, Wingard J R, Burns W H, Hayward S D, Saral R, Perry H R, Santos G W, Hayward G S
J Clin Microbiol. 1985 Mar;21(3):353-6. doi: 10.1128/jcm.21.3.353-356.1985.
An assay for the presence of Epstein-Barr virus (EBV) DNA was developed by using a cloned EBV DNA probe. After preliminary testing showed the assay to be sensitive and specific, it was applied to 135 mouthwashes from bone marrow transplant recipients, and 21 of these tests were positive. The concentration of EBV DNA in mouthwashes in some cases was as high as 10(8) genome equivalents per ml. When compared with the lymphocyte transformation assay on the same samples, the sensitivity was 75% and the specificity was 97%. In contrast to the lymphocyte transformation assay, the hybridization was semiquantitative and yielded results in 72 h. Potential applications include monitoring the effects of various interventions, such as immunosuppressive and antiviral chemotherapy, on EBV shedding.
利用克隆的爱泼斯坦-巴尔病毒(EBV)DNA探针开发了一种检测EBV DNA存在的检测方法。初步测试表明该检测方法灵敏且特异后,将其应用于135份骨髓移植受者的漱口水样本,其中21份检测呈阳性。在某些情况下,漱口水样本中EBV DNA的浓度高达每毫升10⁸个基因组当量。与对相同样本进行的淋巴细胞转化试验相比,该杂交检测的灵敏度为75%,特异性为97%。与淋巴细胞转化试验不同,杂交是半定量的,且72小时内即可得出结果。其潜在应用包括监测各种干预措施(如免疫抑制和抗病毒化疗)对EBV脱落的影响。