Devens B, Galili N, Deutsch O, Naor D, Klein E
Eur J Immunol. 1978 Aug;8(8):573-8. doi: 10.1002/eji.1830080807.
Unprimed spleen cells from A and C57BL/6 mice could not produce cytotoxic responses to their syngeneic tumors: a Moloney virus-induced in vitro subline YAC-1 and a Rauscher virus-induced in vitro subline RBL5, respectively. Spleen cells from A and C57BL/6 mice immunized with YAC-1 OR RBL5 (which cross-react serologically) generated significant syngeneic cytotoxicities after cultivation in vitro. The in vivo carried tumor of A mice, unlike the in vitro sublines, could not stimulate a priming effect. In contrast, YAC stimulated the formation of suppressor cells in both A and C57BL/6 mice. The suppressor cells abrogated the priming effect of the syngeneic tumors, but not the priming effect of the allogeneic tumors. Furthermore, YAC did not suppress normal allogeneic anti-tumor responses. The theoretical and the practical implications of these studies are discussed.
来自A系和C57BL/6系小鼠的未致敏脾细胞,分别对其同基因肿瘤(莫洛尼病毒诱导的体外亚系YAC-1和劳舍尔病毒诱导的体外亚系RBL5)无法产生细胞毒性反应。用YAC-1或RBL5(二者存在血清学交叉反应)免疫的A系和C57BL/6系小鼠的脾细胞,在体外培养后产生了显著的同基因细胞毒性。与体外亚系不同,A系小鼠体内携带的肿瘤无法刺激引发效应。相反,YAC在A系和C57BL/6系小鼠中均刺激了抑制细胞的形成。这些抑制细胞消除了同基因肿瘤的引发效应,但并未消除异基因肿瘤的引发效应。此外,YAC并未抑制正常的异基因抗肿瘤反应。本文讨论了这些研究的理论和实际意义。