Watson D B, Burns G F, Mackay I R
J Immunol. 1983 May;130(5):2442-7.
Epstein Barr virus was used to transform the B lymphocytes infiltrating metastatic tumor tissue from seven patients with melanoma. In this way it was possible to establish continuously growing B lymphoblastoid cell lines (LCL) derived from the tumor-infiltrating B lymphocytes from each of the seven patients. Antibody production of up to 50 micrograms/ml could be achieved by such cultures, and the lymphoblastoid cells could be cloned readily by limit dilution on a feeder layer of irradiated fetal fibroblasts. Preliminary analysis of the antibodies produced by lymphoblastoid cell lines established from tumors from two of the patients indicated that most were of IgM type and bound to a panel of melanoma cell target cells, as well as to some nonmelanoma tumor cell lines. Cloned LCL were produced from the tumor-infiltrating B cells from one of the patients, and of 100 such clones tested, 9% secreted antibody that bound to autologous tumor cells, and one of these clones produced antibody that appeared to be melanoma specific.
爱泼斯坦-巴尔病毒被用于转化来自7名黑色素瘤患者转移性肿瘤组织中浸润的B淋巴细胞。通过这种方式,得以建立起源自这7名患者各自肿瘤浸润B淋巴细胞的持续生长的B淋巴母细胞系(LCL)。此类培养物可实现高达50微克/毫升的抗体产生,并且淋巴母细胞可通过在经辐照的胎儿成纤维细胞饲养层上进行有限稀释而轻松克隆。对从两名患者的肿瘤中建立的淋巴母细胞系所产生抗体的初步分析表明,大多数为IgM型,可与一组黑色素瘤细胞靶细胞以及一些非黑色素瘤肿瘤细胞系结合。从其中一名患者的肿瘤浸润B细胞中产生了克隆的LCL,在测试的100个此类克隆中,9%分泌的抗体可与自体肿瘤细胞结合,其中一个克隆产生的抗体似乎是黑色素瘤特异性的。