Stirrat G M
J Immunol Methods. 1976;12(3-4):201-18. doi: 10.1016/0022-1759(76)90042-9.
The development of a terminal-labelling microcytotoxicity assay is described in which target cells (fetal fibroblasts) were labelled with 125I-iododeoxyuridine after effector (lymphoid) cells had been incubated with them for 24 h. The time-course for the development of cell-mediated cytotoxicity was assessed following allogeneic skin grafting. 'Non-specific' cytotoxicity detracts from the sensitivity of all microcytotoxicity assays and the terminal-labelling assay using 125I is no exception. The non-specific effects can be reduced but not eliminated by the removal of adherent cells. The optimum target cell/effector cell ratio would seem to be between 1:100 and 1:250. Residual lymph node cells did not appear to incorporate enough label to affect the test results. In vivo correlates of in vitro findings are still not easy to determine.
本文描述了一种终末标记微细胞毒性测定法的开发,其中在效应(淋巴细胞)细胞与靶细胞(胎儿成纤维细胞)共同孵育24小时后,用125I-碘脱氧尿苷标记靶细胞。在同种异体皮肤移植后评估细胞介导的细胞毒性发展的时间进程。“非特异性”细胞毒性会降低所有微细胞毒性测定法的灵敏度,使用125I的终末标记测定法也不例外。通过去除贴壁细胞,非特异性效应可以降低但不能消除。最佳靶细胞/效应细胞比例似乎在1:100至1:250之间。残留的淋巴结细胞似乎没有摄取足够的标记物来影响测试结果。体外研究结果与体内情况的相关性仍然不易确定。