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活检恶性淋巴瘤细胞中EB病毒的检测及其连续培养

Detection of Epstein-Barr virus in biopsied malignant lymphoma cell and its continuous culture.

作者信息

Suzuki T, Oboshi S, Ishihara N, Emura I, Ohnishi Y, Sairenji T, Hinuma Y

出版信息

Gan. 1978 Apr;69(2):213-21.

PMID:210075
Abstract

In more than 80% of tumor cells in the pericardiac effusion of a case of malignant B-cell lymphoma, Epstein-Barr virus-determined nuclear antigen (EBNA) was detected by the anticomplement immunofluorescence test. Moreover, herpestype virus particles, although few in number, were demonstrated in the nucleus of lymphoma cells by an electron microscope. Tumor cells in the pericardiac effusion were seeded at 98% purity after centrifugation on Ficoll-Conray and, soon after plating, they proliferated continuously without any lag phase of growth or cell death. Therefore, the established cell line was regarded as of tumor cell origin and named Fujimaki-II cell after patient's name. On the other hand, Fujimaki-I cells were established from the biopsied tumor in the same way. These two cell lines, B-lymphocyte in nature, had both EB virus-related antigens and herpes-types virus particles. Heterotransplantation of cultured cells and tumor tissue obtained at autopsy into athymic nude mice was not successful. Transformation of cord blood lymphocytes by the virus released from Fujimaki-II cell also failed. This might be the first case of non-Burkitt type lymphoma in which the EB virus genome was directly detected in the tumor cells.

摘要

在一例恶性B细胞淋巴瘤的心包积液中,超过80%的肿瘤细胞通过抗补体免疫荧光试验检测到爱泼斯坦-巴尔病毒核抗原(EBNA)。此外,通过电子显微镜在淋巴瘤细胞核中发现了疱疹病毒样颗粒,尽管数量很少。心包积液中的肿瘤细胞经Ficoll-Conray离心后纯度达98%,接种后很快持续增殖,无生长延迟期或细胞死亡。因此,建立的细胞系被认为起源于肿瘤细胞,并以患者名字命名为藤卷-II细胞。另一方面,藤卷-I细胞以同样方式从活检肿瘤中建立。这两个细胞系本质上为B淋巴细胞,既有EB病毒相关抗原,又有疱疹病毒样颗粒。将培养细胞和尸检获得的肿瘤组织异种移植到无胸腺裸鼠中未成功。藤卷-II细胞释放的病毒对脐血淋巴细胞的转化也未成功。这可能是首例在肿瘤细胞中直接检测到EB病毒基因组的非伯基特型淋巴瘤。

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