Mantovani A, Evans R, Alexander P
Br J Cancer. 1977 Jul;36(1):35-40. doi: 10.1038/bjc.1977.151.
Spleen cells collected from mice bearing transplanted chemically induced syngeneic fibrosarcomas non-specifically inhibited DNA synthesis of sarcoma and lymphoma target cells in vitro. Splenocytes from mice hyper-immunized against a syngeneic sarcoma specifically inhibited DNA synthesis of the tumour used for immunization. The impairment of tumour-cell DNA synthesis was associated in vitro with cytostasis, and lysis of the target cells was not seen. Since treatment with anti-theta serum and complement did not impair cytostatic action of the spleen cells, and since thymus-deprived animals showed similar activity to normal mice, T lymphocytes were not involved in non-specific cytostasis. Removal of phagocytic adherent cells by carbonyl iron markedly inhibited the cytostatic activity of the spleen cells, suggesting a role in this reaction for cells of the monocyte-macrophage series. The presence of an actively growing sarcoma was a prerequisite for the expression of non-specific cytostasis, since surgical excision resulted in complete disappearance of this activity of spleen cells.
从小鼠体内收集的携带移植性化学诱导同基因纤维肉瘤的脾细胞在体外非特异性抑制肉瘤和淋巴瘤靶细胞的DNA合成。用同基因肉瘤进行超免疫的小鼠的脾细胞特异性抑制用于免疫的肿瘤的DNA合成。肿瘤细胞DNA合成的损害在体外与细胞停滞有关,未观察到靶细胞的裂解。由于用抗θ血清和补体处理不损害脾细胞的细胞抑制作用,并且由于无胸腺动物表现出与正常小鼠相似的活性,T淋巴细胞不参与非特异性细胞停滞。用羰基铁去除吞噬性贴壁细胞显著抑制脾细胞的细胞抑制活性,提示单核细胞-巨噬细胞系列细胞在该反应中起作用。存在活跃生长的肉瘤是表达非特异性细胞停滞的先决条件,因为手术切除导致脾细胞的这种活性完全消失。