Neel H B, Ritts R E
Cancer. 1977 Oct;40(4):1643-9. doi: 10.1002/1097-0142(197710)40:4<1643::aid-cncr2820400437>3.0.co;2-4.
Experiments were designed to assess 1) relative immunity after adoptive transfer of spleen cells or serum from tumor-bearing mice to untreated syngeneic mice, and 2) the degree of tumor-specific transplantation immunity imparted by cells or serum relative to tumor size and the presence of metastases in the donor at the time of spleen cell or serum transfer or after in situ necrosis of the primary tumor by cryosurgery in a CDF1-sarcoma system. Viable lymphoid spleen cells or serum from normal mice had no effect on tumor growth. Serum from mice that had large tumors and gross metastases induced a protective effect similar to that found after cryosurgery of the primary tumor. Serum from mice with small tumors and spleen cells from animals bearing either small or large tumors failed to induce immunity consistently. In no instance did serum from tumor-bearing mice induce enhancement of tumor growth.
1)将荷瘤小鼠的脾细胞或血清过继转移至未处理的同基因小鼠后的相对免疫力;2)在CDF1 -肉瘤系统中,脾细胞或血清转移时或通过冷冻手术使原发肿瘤原位坏死之后,细胞或血清赋予的肿瘤特异性移植免疫力相对于肿瘤大小以及供体中转移灶存在情况的程度。正常小鼠的活淋巴细胞脾细胞或血清对肿瘤生长没有影响。患有大肿瘤和明显转移灶的小鼠血清诱导出的保护作用,与原发肿瘤冷冻手术后的保护作用相似。患有小肿瘤的小鼠血清以及来自患有小肿瘤或大肿瘤动物的脾细胞,均未能持续诱导出免疫力。荷瘤小鼠的血清在任何情况下均未诱导肿瘤生长增强。