Chauvenet P H, McArthur C P, Smith R T
J Immunol. 1979 Dec;123(6):2575-81.
Chemically induced tumors of mice exhibit apparently unique antigenicity upon syngeneic transplantation into appropriately immunized hosts. An in vitro counterpart of this pattern in terms of specificity has not been reported. Data are presented that demonstrate that immune peritoneal exudates contain cells cytotoxic for the specific immunogen tumor but with rare exceptions, not toward other syngeneic methylcholanthrene-induced fibrosarcomas. Only tumors highly immunogenic by transplantation criteria induce cytotoxic PEC regularly; nonimmunogenic tumors consistently fail to do so. The effector cell responsible is eliminated by pretreatment with anti-Thy.1 but not anti-Ig plus complement. In concomitant experiments, PEC populations cytotoxic in vitro also conveyed adoptive protection against the specific tumor in syngeneic hosts. This in vitro assay appears to provide a tool for studying T cell-mediated cytotoxicity toward a set of unique surface antigens present on chemically induced tumors.
化学诱导的小鼠肿瘤在同基因移植到适当免疫的宿主中时表现出明显独特的抗原性。关于这种特异性模式在体外的对应情况尚未见报道。本文提供的数据表明,免疫腹膜渗出液中含有对特定免疫原性肿瘤具有细胞毒性的细胞,但极少数情况除外,这些细胞对其他同基因甲基胆蒽诱导的纤维肉瘤没有细胞毒性。只有根据移植标准具有高度免疫原性的肿瘤才能定期诱导产生细胞毒性的腹膜渗出细胞(PEC);无免疫原性的肿瘤始终无法做到这一点。起作用的效应细胞可通过抗Thy.1预处理而被清除,但抗Ig加补体则不能。在相关实验中,体外具有细胞毒性的PEC群体也能在同基因宿主中对特定肿瘤提供过继性保护。这种体外检测方法似乎为研究针对化学诱导肿瘤上存在的一组独特表面抗原的T细胞介导的细胞毒性提供了一种工具。