Boon T, Van Snick J, Van Pel A, Uyttenhove C, Marchand M
J Exp Med. 1980 Nov 1;152(5):1184-93. doi: 10.1084/jem.152.5.1184.
Tumor cell variants that were rejected by syngeneic mice (tum-) were obtained from mastocytoma P815 by mutagenesis (as described in the accompanying report (13). A considerable T lymphocyte-mediated lysis was observed upon incubation of these tum- variants with peritoneal exudate cells collected a few days after an intraperitoneal challenge of immune animals. Spleen cells from these animals were cytolytic after stimulation in vitro with the immunizing variant. New antigens, absent from the original P815 tum+ cells, were detected on 15 of the 21 tum- variants that were tested. All these antigens appeared to be different. No new antigen was detected on any of 10 mutagenized P815 clones that had retained their ability to form tumors. We compared the evidence obtained in vivo and in vitro for the presence of specific antigens on five tum- variants. Three variants were shown both in vivo and in vitro to carry an individual antigen. One showed no specificity either in vivo or in vitro. However, for one variant, no specificity was observed in vivo, although cytolysis tests demonstrated the existence of a singular antigenic specificity.
通过诱变从肥大细胞瘤P815获得被同基因小鼠排斥的肿瘤细胞变体(tum-)(如随附报告(13)中所述)。将这些tum-变体与免疫动物腹腔内攻击后几天收集的腹腔渗出细胞一起孵育时,观察到相当程度的T淋巴细胞介导的裂解。这些动物的脾细胞在体外用免疫变体刺激后具有细胞溶解性。在测试的21个tum-变体中的15个上检测到原始P815 tum+细胞中不存在的新抗原。所有这些抗原似乎都不同。在10个保留形成肿瘤能力的诱变P815克隆中,没有一个检测到新抗原。我们比较了在体内和体外获得的关于五个tum-变体上存在特异性抗原的证据。三个变体在体内和体外均显示携带单个抗原。一个在体内和体外均未显示出特异性。然而,对于一个变体,尽管细胞溶解试验证明存在单一抗原特异性,但在体内未观察到特异性。