Said W, Chien K, Takeuchi S, Tasaka T, Asou H, Cho S K, de Vos S, Cesarman E, Knowles D M, Koeffler H P
Department of Pathology, Cedars Sinai Medical Center, Los Angeles, CA 90048, USA.
Blood. 1996 Jun 15;87(12):4937-43.
Recent molecular evidence suggests an association with a new herpesvirus, Kaposi's sarcoma-associated herpesvirus (KSHV/HHV-8), and primary effusion lymphomas (PELs). PELs have a characteristic morphology, phenotype, and clinical presentation, with malignant effusions in the absence of a contiguous solid tumor mass. We have established a cell line (KS-1) from a KSHV-positive human immunodeficiency virus (HIV)-negative patient with pleural cavity-based lymphoma that was passaged into triple-immunodeficient BNX mice. In contrast to cell lines from body cavity-based lymphomas derived from HIV-positive individuals that contain both KSHV and Epstein Barr viral genome, these cells contain only KSHV, allowing for uncontaminated virologic studies. Ultrastructural examination identified malignant cells with features of late differentiating B cells (immunoblasts). Cells with viral cytopathic effect contained typical 110-nm intranuclear herpesvirus nucleocapsids and complete cytoplasmic virions, confirming the association of PEL with KSHV.
最近的分子证据表明,一种新的疱疹病毒——卡波西肉瘤相关疱疹病毒(KSHV/HHV-8)与原发性渗出性淋巴瘤(PEL)有关。PEL具有特征性的形态、表型和临床表现,表现为无连续实体瘤块的恶性渗出液。我们从一名KSHV阳性、人类免疫缺陷病毒(HIV)阴性且患有基于胸腔的淋巴瘤患者中建立了一个细胞系(KS-1),并将其接种到三重免疫缺陷的BNX小鼠体内。与来自HIV阳性个体的体腔淋巴瘤细胞系不同,后者同时含有KSHV和EB病毒基因组,而这些细胞仅含有KSHV,这使得进行无污染的病毒学研究成为可能。超微结构检查发现具有晚期分化B细胞(免疫母细胞)特征的恶性细胞。具有病毒细胞病变效应的细胞含有典型的110纳米核内疱疹病毒核衣壳和完整的胞质病毒体,证实了PEL与KSHV的关联。