White L, Trickett A, Norris M D, Tobias V, Sosula L, Marshall G M, Stewart B W
Children's Leukaemia and Cancer Research Unit, Prince of Wales Children's Hospital, Sydney, New South Wales, Australia.
Cancer Res. 1990 May 15;50(10):3078-86.
There are few effective models for the study of human lymphoid neoplasms, including in vivo xenografts in immunocompromised animals. Exploiting the additional immune privilege of the anterior chamber of the nude mouse eye, a novel method of direct heterotransplantation of cells from childhood leukemias and lymphomas has been developed. The establishment and characterization of 18 lymphoid xenograft cell lines maintained in the nude mouse intraocular model are reported. Cell sources for heterotransplantation were specimens of bone marrow, peripheral blood, or lymphomatous masses obtained at either diagnosis or recurrence of disease in the patients. The 18 patients and resultant cell lines were grouped into four immunophenotypic categories: Category 1, B-lineage (pre-B and early pre-B), "common" acute lymphatic leukemias; Category 2, cell lines of similar immunophenotype derived from patients with unusual features; Category 3, B-cell neoplasms and cell lines; and Category 4, neoplasms and cell lines in part or totally of T-cell origin. With reference to these groupings, rates of ingraftment from clinical specimens varied according to immunophenotype and disease status: Category 1, 1 of 15 at diagnosis, 5 of 7 at relapse; Category 2, 1 of 1 at diagnosis, 2 of 2 at relapse; Category 3, 6 of 6 at diagnosis; and Category 4, 2 of 9 at diagnosis, 1 of 1 with persistent disease. Rearrangements of the genes for immunoglobulin heavy chain or kappa light chain and for beta subunit of the T-cell receptor gene were demonstrated according to immunophenotype, with the exception of one cell line which showed no rearrangements. Evidence of Epstein-Barr virus DNA was shown in only one cell line, of B-cell immunophenotype. Cytology, histopathology, and electron microscopy in representative patient and xenograft samples demonstrated correlations between the specimens of origin and cells or sections from ingrafted tumors in mice. It is concluded that the direct heterotransplantation of cells from childhood leukemias and lymphomas to the anterior chamber of the nude mouse eye provides a relevant and reproducible model for the maintenance and study of human lymphoid neoplasms.
对于人类淋巴肿瘤的研究,几乎没有有效的模型,包括免疫缺陷动物体内的异种移植。利用裸鼠眼前房额外的免疫赦免特性,已经开发出一种将儿童白血病和淋巴瘤细胞直接进行异种移植的新方法。本文报道了在裸鼠眼内模型中维持的18种淋巴异种移植细胞系的建立及特征。异种移植的细胞来源是患者在疾病诊断或复发时获取的骨髓、外周血或淋巴瘤肿块标本。这18例患者及由此产生的细胞系被分为四个免疫表型类别:第1类,B系(前B和早前B)“常见”急性淋巴细胞白血病;第2类,来自具有不寻常特征患者的免疫表型相似的细胞系;第3类,B细胞肿瘤和细胞系;第4类,部分或完全起源于T细胞的肿瘤和细胞系。参照这些分组,临床标本的植入率因免疫表型和疾病状态而异:第1类,诊断时15例中有1例,复发时7例中有5例;第2类,诊断时1例中有1例,复发时2例中有2例;第3类,诊断时6例中有6例;第4类,诊断时9例中有2例,持续性疾病患者1例中有1例。根据免疫表型证实了免疫球蛋白重链或κ轻链基因以及T细胞受体基因β亚基基因的重排,但有一个细胞系未显示重排。仅在一个B细胞免疫表型的细胞系中显示出爱泼斯坦-巴尔病毒DNA的证据。代表性患者和异种移植样本的细胞学、组织病理学和电子显微镜检查表明,起源标本与小鼠移植肿瘤的细胞或切片之间存在相关性。结论是,将儿童白血病和淋巴瘤细胞直接异种移植到裸鼠眼前房为人类淋巴肿瘤的维持和研究提供了一个相关且可重复的模型。