Gautam S C, Deodhar S D
Cancer Res. 1979 Aug;39(8):2945-51.
Spleen cells of C57BL/6J mice bearing a poorly immunogenic syngeneic tumor T241 have been shown to suppress the mitogen-induced proliferative responses of normal spleen cells. However, no suppressive effect of these cells was observed on the generation of cytotoxic cells following immunization in vitro against H-2 histocompatibility antigens. The suppressor activity disappeared rapidly after the removal of the primary tumor. Spleen cells of tumor-bearing mice also suppressed the mitogen-induced stimulation of normal spleen cells of mice of different H-2 loci. Removal of phagocytic cells with carbonyl iron treatment had very little effect on the suppressor activity. Suppressor activity was enhanced following fractionation of cells through nylon wool columns. The suppressor population was found to resist anti-immunoglobulin serum and complement treatment, but treatment with anti-thymocyte serum and complement drastically reduced the suppressor activity. These results indicate that cells with suppressor activity have characteristics of T-lymphocytes.
携带低免疫原性同基因肿瘤T241的C57BL/6J小鼠的脾细胞已被证明可抑制正常脾细胞的丝裂原诱导的增殖反应。然而,在体外针对H-2组织相容性抗原免疫后,未观察到这些细胞对细胞毒性细胞的产生有抑制作用。去除原发性肿瘤后,抑制活性迅速消失。荷瘤小鼠的脾细胞也抑制了不同H-2位点小鼠正常脾细胞的丝裂原诱导的刺激。用羰基铁处理去除吞噬细胞对抑制活性影响很小。通过尼龙毛柱对细胞进行分级分离后,抑制活性增强。发现抑制细胞群体可抵抗抗免疫球蛋白血清和补体处理,但用抗胸腺细胞血清和补体处理可大大降低抑制活性。这些结果表明,具有抑制活性的细胞具有T淋巴细胞的特征。