Musiani M, Zerbini M, Plazzi M, Gentilomi G, La Placa M
Institute of Microbiology, University of Bologna, Italy.
J Clin Microbiol. 1988 May;26(5):1005-8. doi: 10.1128/jcm.26.5.1005-1008.1988.
An immunocytochemical staining for the detection of antibody to Epstein-Barr virus nuclear antigen in cell smears was developed by using a three-dimensional complex of streptavidin and biotin labeled with horseradish peroxidase as the detector system. The presence of antibody against Epstein-Barr virus nuclear antigen was revealed by a dark staining of the nuclei of Raji cells. A significant correlation was found between the titers obtained with our assay and titers obtained by anticomplement immunofluorescence on 110 serum samples. Our assay did not require an Epstein-Barr virus-negative serum source for fresh complement and gave a permanent record of the reaction that could easily be observed under an ordinary light microscope.
通过使用辣根过氧化物酶标记的链霉亲和素和生物素的三维复合物作为检测系统,开发了一种用于检测细胞涂片中华氏巨细胞病毒核抗原抗体的免疫细胞化学染色方法。通过Raji细胞核的深色染色揭示了针对华氏巨细胞病毒核抗原的抗体的存在。在110份血清样本中,我们的检测方法所获得的滴度与抗补体免疫荧光法所获得的滴度之间发现了显著相关性。我们的检测方法不需要新鲜补体的爱泼斯坦-巴尔病毒阴性血清来源,并且给出了反应的永久记录,该记录可以在普通光学显微镜下轻松观察到。