Brunner K T, Mauel J, Schindler R
Immunology. 1966 Nov;11(5):499-506.
The reaction between sensitized lymphoid cells and target cells has been studied in an allogeneic transplantation system in mice. Mastocytoma cells of the DBA/2 donor strain were injected into C57BL mice, and the spleens of the recipients harvested 8 days later. The immune lymphoid cells thus obtained were tested for their ability to damage cultures of target mastocytoma cells. The reaction was followed by two methods: (1) microscopic counts, and (2) ability of target cells to form colonies in a semi-solid medium after various periods of contact with immune lymphoid cells. The results show: (a) that the effect on target cells is an exponential function of the number of immune lymphoid cells employed, and (b) that the reaction becomes noticeable after 3 hours and reaches completion within 12 hours when evaluated by cloning techniques, while it takes 24–48 hours to be microscopically clearly demonstrable. Problems arising from use of both methods are discussed.
在小鼠的同种异体移植系统中,对致敏淋巴细胞与靶细胞之间的反应进行了研究。将DBA/2供体品系的肥大细胞瘤细胞注入C57BL小鼠体内,8天后采集受体的脾脏。对由此获得的免疫淋巴细胞损伤靶肥大细胞瘤细胞培养物的能力进行了检测。该反应通过两种方法进行跟踪:(1)显微镜计数,以及(2)在与免疫淋巴细胞接触不同时间段后,靶细胞在半固体培养基中形成集落的能力。结果表明:(a)对靶细胞的影响是所用免疫淋巴细胞数量的指数函数,并且(b)当通过克隆技术评估时,反应在3小时后变得明显,并在12小时内完成,而在显微镜下清晰显示则需要24 - 48小时。讨论了使用这两种方法时出现的问题。