Moscovitch M, Kaufmann Y, Berke G
J Immunol. 1984 Nov;133(5):2369-74.
We have previously described monoclonal CTL-hybridomas growing continuously in culture in the absence of a known antigenic stimulus or growth-promoting factor(s), exhibiting specific anti-H-2Db killing activity in vitro after a distinct 2-hr lag period before the onset of lysis. Here we provide evidence indicating that the hybridoma Md 26.15 represents "memory" CTL, and we examine the mechanism whereby they respond to antigen/mitogen. The brief period (2 to 3 hr) required for stimulation suggests that expression of potentiated effector function(s) after stimulation requires no cell replication. The frequency of effector hybridoma cells capable of specific binding to target cells before and after stimulation is the same, as determined in a direct hybridoma-target cell conjugation test, although cytolytic activity is markedly enhanced. On the other hand, kinetic and cell dispersion assays indicate that the potentiation of cytolytic activity can be attributed to shortening of the lag period of killing as well as to a small enhancement in the recycling ability of cytolytic effectors. We suggest that shortening of the lag period involves activation of potential effectors, which is manifested at a post-binding stage of effector-target interaction. The CTL hybridoma described herein provides a unique model system for studying CTL reactivation.
我们之前曾描述过在没有已知抗原刺激或生长促进因子的情况下在培养中持续生长的单克隆CTL杂交瘤,在裂解开始前有明显的2小时延迟期后,它们在体外表现出特异性的抗H-2Db杀伤活性。在此,我们提供证据表明杂交瘤Md 26.15代表“记忆”CTL,并研究它们对抗原/丝裂原作出反应的机制。刺激所需的短暂时间(2至3小时)表明,刺激后增强的效应器功能的表达不需要细胞复制。在直接的杂交瘤-靶细胞结合试验中确定,刺激前后能够特异性结合靶细胞的效应杂交瘤细胞的频率相同,尽管细胞溶解活性明显增强。另一方面,动力学和细胞分散分析表明,细胞溶解活性的增强可归因于杀伤延迟期的缩短以及细胞溶解效应器循环能力的小幅增强。我们认为延迟期的缩短涉及潜在效应器的激活,这在效应器-靶标相互作用的结合后阶段表现出来。本文所述的CTL杂交瘤为研究CTL再激活提供了一个独特的模型系统。