Sensitization of rat T cells to syngeneic tumor cultures by cocultivation in diffusion chambers.

S Cornain, S Becker, E Klein
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Abstract

Total population and T cell enriched fractions of rat spleen were cultivated in diffusion chambers implanted intraperitoneally to mice and rats. 10-16% of the input cells were recovered after 5 days. When the chambers were carried in the xenogeneic environment activation occurred as indicated by blastogenesis and non-discriminative cytotoxicity. Specific activation of the T population was induced by mixed lymphocyte-tumor culture in chambers implanted in rats. The presence of tumor cells induced blastogenesis, elevation of the proportion of Fc receptor positive cells and generated cytotoxic cells to the sensitizer tumor. The precursor of cytotoxic cells did not have Fc or C3 receptors since nylon wool colum passed fractions depleted from these cells by elimination of EA- or EAC-rosettes were also activated.

扩散室共培养大鼠T细胞对同源肿瘤的致敏作用。
在小鼠和大鼠腹腔内的扩散室中培养大鼠脾总细胞和T细胞富集部分。5 d后10-16%的输入细胞恢复。当囊室在异种环境中携带时,激活发生,如胚发生和非歧视性细胞毒性所示。通过在大鼠植入腔内的混合淋巴细胞肿瘤培养,诱导T细胞群的特异性激活。肿瘤细胞的存在诱导了胚胎发生,Fc受体阳性细胞的比例升高,产生了对致敏肿瘤的细胞毒性细胞。细胞毒性细胞的前体没有Fc或C3受体,因为通过消除EA-或eac -莲座从这些细胞中消耗的尼龙羊毛柱通过的分数也被激活。
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