Parker G A, Rosenberg S A
J Natl Cancer Inst. 1977 May;58(5):1303-9. doi: 10.1093/jnci/58.5.1303.
The humoral immune response to two transplanted chemically induced murine sarcomas (MCA-2 and MCA-3) was studied in C57BL/6N mice. These tumors were immunogenic as evidenced by tumor amputation and rechallenge experiments, and no cross-reactivity between them was observed in in vivo challenge experiments. Utilizing a complement-dependent microcytotoxicity assay, we detected antibody to both MCA-2 and MCA-3 in the sera of animals bearing MCA-3 as well as after tumor removal. The sera of animals hyperimmunized to MCA-3 (MCA-3HI) was also cytotoxic in high titer to both MCA-2 and MCA-3 (50% cytotoxicity titers of 1:80 and 1:320, respectively). Sequential absorptions of sera from animals bearing MCA-3 and MCA-3HI sera with fresh MCA-2 cells completely removed activity against MCA-2 but retained reactivity to MCA-3. Sequential absorptions with fresh MCA-3 cells produced stepwise reductions of activity against both tumors, whereas absorption with normal cells produced no loss of activity against either tumor. Thus both specific and cross-reactive antigens were expressed on the surfaces of MCA-3 cells. Only the specific tumor antigen appeared to be involved in in vivo protection against tumor challenge.
在C57BL/6N小鼠中研究了对两种移植的化学诱导小鼠肉瘤(MCA - 2和MCA - 3)的体液免疫反应。这些肿瘤具有免疫原性,肿瘤切除和再攻击实验证明了这一点,并且在体内攻击实验中未观察到它们之间的交叉反应性。利用补体依赖性微细胞毒性试验,我们在携带MCA - 3的动物血清中以及肿瘤切除后检测到了针对MCA - 2和MCA - 3的抗体。对MCA - 3进行超免疫的动物(MCA - 3HI)的血清对MCA - 2和MCA - 3也具有高滴度的细胞毒性(50%细胞毒性滴度分别为1:80和1:320)。用新鲜的MCA - 2细胞对携带MCA - 3的动物血清和MCA - 3HI血清进行连续吸收,完全消除了针对MCA - 2的活性,但保留了对MCA - 3的反应性。用新鲜的MCA - 3细胞进行连续吸收导致对两种肿瘤的活性逐步降低,而用正常细胞吸收则未导致对任何一种肿瘤的活性丧失。因此,特异性和交叉反应性抗原都在MCA - 3细胞表面表达。只有特异性肿瘤抗原似乎参与了体内对肿瘤攻击的保护作用。