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一种以125I-碘脱氧尿苷作为靶细胞标记物的终末标记微量细胞毒性试验。

A terminal-labelling microcytotoxicity assay with 125I-iododeoxyuridine as a label for target cells.

作者信息

Stirrat G M

出版信息

J Immunol Methods. 1976;12(3-4):201-18. doi: 10.1016/0022-1759(76)90042-9.

Abstract

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.

摘要

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。

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[3H]Uridine uptake by target monolayers as a terminal label in an in vitro cell-mediated cytotoxicity assay.
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