Devens B, Naor D
J Immunol. 1979 Apr;122(4):1397-401.
Splenocytes from A mice injected with YAC-1 or RBL5 could generate, after in vitro culture with or without stimulation, a genetically nonrestricted cytotoxic response against the allogenic tumor RBL5. YAC-1 tumor is an in vitro carried tumor induced in A mice (H-2a) by Moloney virus. RBL5 tumor is a Rauscher virus-induced tumor of C57BL/6 mice (H-2b). These tumors cross-react serologically. The effector cells that were generated after the in vitro cultivation recognized tumor-associated antigens on the target cells. H-2 alloantigens were not recognized by the effector cells. The effector cells that killed RBL5 tumor in a genetically nonrestricted manner were identified as T cells. The in vivo carried tumor YAC, in contrast to the in vitro carried tumor YAC-1, could not induce anti-RBL5 reactive cells in A mice. Instead, YAC tumor induced suppressor cells in A mice, which could abrogate the anti-RBL5 cytotoxic response of RBL5-primed splenocytes, but not that of YAC-1 primed splenocytes.
用YAC-1或RBL5注射的A系小鼠的脾细胞,在体外培养(有无刺激)后,可产生针对同种异体肿瘤RBL5的基因非限制性细胞毒性反应。YAC-1肿瘤是由莫洛尼病毒在A系小鼠(H-2a)体内诱导产生的体外携带肿瘤。RBL5肿瘤是劳舍尔病毒诱导的C57BL/6小鼠(H-2b)的肿瘤。这些肿瘤在血清学上发生交叉反应。体外培养后产生的效应细胞识别靶细胞上的肿瘤相关抗原。效应细胞不识别H-2同种异体抗原。以基因非限制性方式杀伤RBL5肿瘤的效应细胞被鉴定为T细胞。与体外携带的肿瘤YAC-1相比,体内携带的肿瘤YAC不能在A系小鼠中诱导抗RBL5反应性细胞。相反,YAC肿瘤在A系小鼠中诱导产生抑制细胞,该抑制细胞可消除RBL5致敏脾细胞的抗RBL5细胞毒性反应,但不能消除YAC-1致敏脾细胞的抗RBL5细胞毒性反应。