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通过测量增殖靶细胞(K 562细胞系)的DNA合成来测定人外周血淋巴细胞的自然杀伤活性。

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

作者信息

Huttunen K, Ilonen J

出版信息

Acta Pathol Microbiol Immunol Scand C. 1983 Jun;91(3):197-201.

PMID:6880751
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.

摘要

通过测量单独的以及在效应细胞存在情况下3H-胸腺嘧啶核苷掺入增殖性高NK敏感性K562靶细胞中的情况,来测定人外周血淋巴细胞的自然杀伤(NK)活性。尽管绝对数值有所不同,主要取决于测定当天靶细胞DNA合成的强度,但结果具有高度可重复性,并且与51Cr释放试验(CRA)的结果相当。该方法极其简单,比CRA操作更简便。通过纳入已知的低NK活性和高NK活性对照细胞,便于对数据进行解释。对NK活性不太敏感的细胞似乎不适合这种检测。

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