Veit B C, Feldman J D
Int J Cancer. 1975 Mar 15;15(3):367-76. doi: 10.1002/ijc.2910150302.
Cell-mediated cytotoxicity in the primary immune response to Moloney sarcoma tumor (MST) in allogeneic and syngeneic rats was found to be predominantly T-cell-dependent. A minor non-T-cell cytotoxic activity may also have been detected. CMC was presumably directed against tumor and viral related antigens in the syngeneic host and primarily against alloantigens in the allogeneic host. CMC was more virgorous in the syngeneic host. This may be due to differences in quantities or immunogenicities of the various antigens involved. Two peaks of T-cells in effector populations were observed during a 20-day post-inoculation period. The first peak corresponded to peak T-cell-mediated cytotoxicity on day 8 and the second peak occurred on days 13 or 14 when CMC was minimal or undetectable.
在同种异体和同基因大鼠对莫洛尼肉瘤肿瘤(MST)的初次免疫反应中,发现细胞介导的细胞毒性主要依赖于T细胞。也可能检测到了轻微的非T细胞细胞毒性活性。在同基因宿主中,细胞介导的细胞毒性(CMC)大概是针对肿瘤和病毒相关抗原,而在同种异体宿主中主要针对同种异体抗原。CMC在同基因宿主中更活跃。这可能是由于所涉及的各种抗原在数量或免疫原性上的差异。在接种后20天的时间段内,在效应细胞群体中观察到两个T细胞峰。第一个峰与第8天T细胞介导的细胞毒性峰值相对应,第二个峰出现在第13或14天,此时CMC最小或无法检测到。