The determination of natural killer activity of human peripheral blood lymphocytes by measuring the DNA-synthesis of proliferating target cells (K 562 cell line).

K Huttunen, J Ilonen
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Abstract

Natural killer (NK) activity of human peripheral blood lymphocytes was determined by measuring 3H-thymidine incorporation into proliferating highly NK-sensitive K 562 target cells alone and in the presence of effector cells. Although the absolute figures varied, depending mostly on the strength of DNA-synthesis of the target cells on the day of the assay, the results were highly reproducible and compared well with those of the 51Cr-release assay (CRA). The method was extremely simple and less tedious than CRA. The interpretation of the data was facilitated by including known control cells of low and high NK activity. The cells less sensitive to NK activity did not seem to be suited for this kind of assay.

通过测定增殖靶细胞(k562细胞系)dna合成来测定人外周血淋巴细胞的自然杀伤活性。
通过测定3h -胸腺嘧啶掺入增殖的高度NK敏感的k562靶细胞和在效应细胞存在的情况下测定人外周血淋巴细胞的NK活性。虽然绝对数字不同,主要取决于实验当天靶细胞的dna合成强度,但结果具有高度可重复性,并且与51cr释放试验(CRA)的结果相比良好。与CRA相比,该方法极其简单,不那么繁琐。通过包括已知的低NK活性和高NK活性的对照细胞,促进了数据的解释。对NK活性不太敏感的细胞似乎不适合这种实验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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