健康和患者人群中低NK活性个体自然杀伤细胞的表型和功能分析。

Natural immunity Pub Date : 1995-09-01
F Nagao, T Yabe, M Xu, K Okumura
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摘要

我们通过对比健康个体和患者来研究自然杀伤细胞(NK)活性的缺乏。采用Eu-DTPA释放法测定了68例健康供体和57例患者(36例自身免疫性疾病患者和21例癌症患者)的125例人NK活性,靶细胞用非放射性物质Eu-DTPA标记,并用三色流式细胞术对其进行表型分析。此外,部分供体在PBL中筛选的NK细胞上进行功能研究。23.3%的健康供者和约70%的患者NK活性(LNK)较低。在这些健康LNK和患者LNK中,PBL中CD3-CD16+CD56+亚群的数量明显低于具有高NK活性和中等NK活性(HMNK)的健康个体的相同亚群。从PBL中分离出的CD3-CD16+CD56+细胞在健康LNK和患者LNK中的细胞毒性与健康HMNK大致相同或高于健康HMNK。在正常HMNK、正常LNK和患者LNK中,CD3-CD56+ NK细胞上CD2和LFA-1抗原的表达以及这些细胞中颗粒蛋白如穿孔素和颗粒酶A的数量均无差异。这些结果表明,健康LNK和患者LNK的低NK活性更多地反映在PBL中CD3-CD16+CD56+亚群的减少,而不是NK细胞的功能缺陷。健康LNK的表型和功能研究尚未被广泛报道,我们在本研究中发现了健康LNK和患者LNK之间的一些差异。在IL-2刺激下,健康LNK的细胞毒性比患者LNK增加得更快,且在高效靶细胞比(>或= 40)时,其细胞毒性显著高于患者LNK。健康LNK的PBL中CD3+CD16+/CD56+亚群的数量高于患者LNK,但与健康HMNK的数量基本相同。
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Phenotypical and functional analyses of natural killer cells from low NK activity individuals among healthy and patient populations.

We investigated the deficiency of natural killer (NK) activity by contrasting healthy individuals with patients. Human NK activities of 125 individuals consisting of 68 healthy donors and 57 patients (36 autoimmune disease and 21 cancer patients) were measured by Eu-DTPA release assay in which the target cells were labeled by nonradioactive materials-Eu-DTPA, and they were phenotypically analyzed with three-color flow cytometry. Furthermore, a part of these donors was functionally studied on NK cells sorted out from PBL. 23.3% of healthy donors and approximately 70% of patients had low NK activity (LNK). In these healthy LNK and patient LNK, the population of CD3-CD16+CD56+ subset in PBL was significantly lower than that of the same subset in healthy individuals with high and medium NK activity (HMNK). The cytotoxicity of CD3-CD16+CD56+ cells sorted out from PBL in healthy LNK and patient LNK were approximately the same with or higher than that in healthy HMNK. No differences were found either in the expression of CD2 and LFA-1 antigens on the CD3-CD56+ NK cells or in the amount of granulous proteins such as perforin and granzyme A in these cells among healthy HMNK, healthy LNK and patient LNK. These results suggested that low NK activity of healthy LNK and patient LNK was more reflected by the diminution of the population of CD3-CD16+CD56+ subset in PBL rather than the functional defects of NK cells. A phenotypical and functional study on healthy LNK has not been reported extensively, and we found several differences between healthy LNK and patient LNK in this study. By stimulation with IL-2, the cytotoxicity of healthy LNK increased more rapidly than that of patient LNK, and at high effector:target cell ratio (> or = 40) it was significantly higher than that of patient LNK. The population of CD3+CD16+/CD56+ subset in PBL of healthy LNK was higher than that of patient LNK, but on the other hand it was about the same as that of healthy HMNK.

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Author Index Vol. 16, 1998 Subject Index Vol. 16, 1998 Contents Vol. 16, 1998 Preliminary Pages Session I: Ontogeny and Differentiation of NK and NK-Like Cells
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