Carbone A, Cilia A M, Gloghini A, Capello D, Perin T, Bontempo D, Canzonieri V, Tirelli U, Volpe R, Gaidano G
Division of Pathology, Centro di Riferimento Oncologico, IRCCS, Istituto Nazionale Tumori, Aviano, Italy.
Leuk Lymphoma. 2000 Feb;36(5-6):447-56. doi: 10.3109/10428190009148391.
Primary effusion lymphoma (PEL) is a novel lymphoma entity consistently infected by HHV-8 that occurs predominantly in immunodeficient patients and is characterized by liquid growth in the serous body cavities. In order to facilitate the understanding of PEL pathogenesis and histogenesis, we have established three PEL cell lines termed CRO-AP/2, CRO-AP/3 and CRO-AP/5. All cell lines have been derived from HIV positive homosexual men affected by PEL with (in the case of CRO-AP/2 and CRO-AP/5) or without (in the case of CRO-AP/3) a previous history of Kaposi's sarcoma. The cell lines are representative of both virologic variants of PEL, i.e. HHV-8+ EBV+ PEL (CRO-AP/2 and CRO-AP/5) and HHV-8+ EBV- PEL (CRO-AP/3). Morphologic and phenotypic features of CRO-AP/2, CRO-AP/3 and CRO-AP/5 are typical of PEL, and include morphology bridging immunoblastic and anaplastic features as well as an indeterminate (non B- non T-cell) phenotype. The B-cell nature of the cell lines is documented by the presence of rearranged immunoglobulin genes. The detailed analysis of the molecular and phenotypic features of CRO-AP/2, CRO-AP/3 and CRO-AP/5 has allowed the identification of recurrent chromosomal abnormalities of PEL and has contributed to the definition of PEL as a lymphoma of post-germinal center, pre-terminally differentiated B-cells.
原发性渗出性淋巴瘤(PEL)是一种新型淋巴瘤实体,始终受到HHV - 8感染,主要发生于免疫缺陷患者,其特征是在浆膜体腔内呈液体生长。为了便于理解PEL的发病机制和组织发生,我们建立了三种PEL细胞系,分别称为CRO - AP/2、CRO - AP/3和CRO - AP/5。所有细胞系均来源于受PEL影响的HIV阳性同性恋男性,其中CRO - AP/2和CRO - AP/5有卡波西肉瘤病史,而CRO - AP/3没有。这些细胞系代表了PEL的两种病毒学变体,即HHV - 8 + EBV + PEL(CRO - AP/2和CRO - AP/5)和HHV - 8 + EBV - PEL(CRO - AP/3)。CRO - AP/2、CRO - AP/3和CRO - AP/5的形态学和表型特征是PEL的典型特征,包括兼具免疫母细胞和间变性特征的形态以及不确定的(非B非T细胞)表型。细胞系的B细胞性质通过重排免疫球蛋白基因的存在得以证明。对CRO - AP/2、CRO - AP/3和CRO - AP/5的分子和表型特征的详细分析,使得能够识别PEL反复出现的染色体异常,并有助于将PEL定义为生发中心后、终末分化前B细胞的淋巴瘤。