Chang K L, Albújar P F, Chen Y Y, Johnson R M, Weiss L M
Division of Pathology, City of Hope National Medical Center, Duarte, CA 91010.
Blood. 1993 Jan 15;81(2):496-501.
The Epstein-Barr virus (EBV) has been implicated in the pathogenesis of Hodgkin's disease (HD). This study was undertaken to determine whether the association of EBV with HD showed geographical variation, as in Burkitt's lymphoma. We studied 32 formalin-fixed, paraffin-embedded cases of HD occurring in Peru. EBV DNA-RNA in situ hybridization was performed using a 30-base biotinylated antisense oligonucleotide complementary to the EBER1 gene of EBV. EBV immunohistochemistry was also performed, using a monoclonal antibody (MoAb) to the latent membrane protein (LMP1) of EBV. Identification of the precise cellular subset staining with EBV was accomplished via double-labeling with MoAbs directed against Reed-Sternberg cells (LeuM1/CD15) and B cells (L26/CD20). EBV RNA was identified in all or virtually all of the Reed-Sternberg cells and variants in 30 of the 32 (94%) cases of HD by in situ hybridization. LMP1 expression was identified in 83% of the EBER1-positive cases. Double-labeling studies confirmed the localization of EBV RNA to CD15-expressing Hodgkin's cells. This study found an extremely high prevalence of EBV in Peruvian HD, in contrast to the much lower percentage of EBV-associated cases of HD occurring in "Western" patients.
爱泼斯坦-巴尔病毒(EBV)被认为与霍奇金淋巴瘤(HD)的发病机制有关。本研究旨在确定EBV与HD的关联是否如在伯基特淋巴瘤中那样存在地理差异。我们研究了32例发生在秘鲁的经福尔马林固定、石蜡包埋的HD病例。使用与EBV的EBER1基因互补的30个碱基的生物素化反义寡核苷酸进行EBV DNA-RNA原位杂交。还使用针对EBV潜伏膜蛋白(LMP1)的单克隆抗体(MoAb)进行了EBV免疫组织化学检测。通过用针对里德-斯腾伯格细胞(LeuM1/CD15)和B细胞(L26/CD20)的MoAb进行双重标记,确定了EBV染色的精确细胞亚群。通过原位杂交,在32例HD病例中的30例(94%)的所有或几乎所有里德-斯腾伯格细胞及其变体中检测到了EBV RNA。在83%的EBER1阳性病例中检测到LMP1表达。双重标记研究证实了EBV RNA定位于表达CD15的霍奇金细胞。本研究发现秘鲁HD中EBV的患病率极高,这与“西方”患者中EBV相关HD病例的低得多的比例形成对比。