Bernstein I D, Wright P W, Cohen E
J Immunol. 1976 May;116(5):1367-72.
Spleen cells from W/Fu rats 4 to 6 weeks after immunization with syngeneic Gross virus-induced lymphoma (C58NT)D cells usually lack detectable activity in a short-term 51Cr release assay. The results presented here demonstrate that these spleen cells retain the capacity to generate significant proliferative and cytotoxic activity upon re-exposure to mitomycin C-treated (C58NT)D cells in vitro. Optimal conditions were defined in W/Fu rats for this secondary immune response in vitro to the (C58NT)D cells. The cytotoxic response was observed to be quantitative, reproducible, and specific. Optimal generation occurred 5 days after initiation of cultures with a 30:1 responding cell:stimulating cell ratio. In vitro generated cytotoxic cells inhibit tumor growth in vivo when administered as a mixture with tumor cells.
用同基因格罗斯病毒诱导的淋巴瘤(C58NT)D细胞免疫4至6周后的W/Fu大鼠的脾细胞,在短期51Cr释放试验中通常缺乏可检测到的活性。本文给出的结果表明,这些脾细胞在体外再次接触丝裂霉素C处理的(C58NT)D细胞时,仍保留产生显著增殖和细胞毒性活性的能力。在W/Fu大鼠中确定了体外对(C58NT)D细胞的这种二次免疫反应的最佳条件。观察到细胞毒性反应是定量的、可重复的和特异性的。当以30:1的反应细胞:刺激细胞比例开始培养5天后,出现最佳生成。体外产生的细胞毒性细胞与肿瘤细胞混合给药时可抑制体内肿瘤生长。