Weiss L M, Movahed L A, Warnke R A, Sklar J
Department of Pathology, Stanford University, Calif.
N Engl J Med. 1989 Feb 23;320(8):502-6. doi: 10.1056/NEJM198902233200806.
We used slot blot hybridization, Southern blot hybridization, and in situ hybridization to investigate the presence of Epstein-Barr virus (EBV) genomes in biopsy tissues from patients with Hodgkin's disease. Slot blot hybridization performed on DNA of tissue specimens from 16 patients revealed that biopsy tissue from 3 (19 percent) contained EBV DNA. Southern blot hybridization with a DNA probe containing the 500-base-pair tandem repeated sequences located at the termini of the EBV genome confirmed the findings of the slot blot hybridization in the three positive tissue specimens and indicated the monoclonality of the EBV-infected cells in such tissues. In situ hybridization performed on the three positive specimens and on two from a previous study localized EBV nucleic acid to the Reed-Sternberg cells and variants in all specimens, with intense hybridization to Reed-Sternberg cells in two, less intense but consistent hybridization to Reed-Sternberg cells in two, and focal hybridization to Reed-Sternberg cells in one. We conclude that EBV genomes are present within Reed-Sternberg cells and variants in some patients with Hodgkin's disease and that the infected cells are monoclonal.
我们使用狭缝印迹杂交、Southern印迹杂交和原位杂交技术,来研究霍奇金病患者活检组织中是否存在爱泼斯坦-巴尔病毒(EBV)基因组。对16例患者组织标本的DNA进行狭缝印迹杂交,结果显示,3例(19%)患者的活检组织含有EBV DNA。用包含位于EBV基因组末端的500个碱基对串联重复序列的DNA探针进行Southern印迹杂交,证实了3份阳性组织标本狭缝印迹杂交的结果,并表明此类组织中EBV感染细胞的单克隆性。对3份阳性标本以及之前研究中的2份标本进行原位杂交,结果显示,在所有标本中EBV核酸均定位于里德-斯腾伯格细胞及其变异细胞,其中2份标本里德-斯腾伯格细胞有强烈杂交信号,2份标本里德-斯腾伯格细胞杂交信号较弱但一致,1份标本里德-斯腾伯格细胞有局灶性杂交信号。我们得出结论,在一些霍奇金病患者的里德-斯腾伯格细胞及其变异细胞中存在EBV基因组,且感染细胞为单克隆性。