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[白细胞介素-2和β干扰素对经聚蔗糖分离的大颗粒淋巴细胞组分杀伤自体肿瘤细胞的作用]

[The effect of IL-2 and IFN-beta on autologous tumor cell kill by Percoll separated LGL fractions].

作者信息

Ezaki K

机构信息

Department of Internal Medicine, School of Medicine, Fujita-Gakuen Health University.

出版信息

Hum Cell. 1988 Mar;1(1):60-4.

PMID:3154015
Abstract

Low density fractions of Percoll density gradient centrifugation of peripheral mononuclear cells contained the majority of large granular lymphocytes (LGL). LGL were used for 5-hr 51Cr release cytotoxic assay against autologous tumor cells in 20 patients with hematological malignancies (9AML, 4ALL and 7NHL). Mean % cytotoxicity (% CTX) was 6.0%, and the addition of IFN-beta and IL-2 in the medium induced the significant increase of % CTX to 15.0% and 26.1%, respectively. When LGL cultured in medium containing IFN-beta and IL-2 were assessed for cytotoxicity daily for 8 days, the enhancement of % CTX by IFN-beta was declined in a few days, while the enhancement by IL-2 was sustained for more than 8 days. The pretreatment of LGL with anti Leu-11 (CD16) plus complement abrogated the enhancing effect by IFN-beta or IL-2, but not with anti Leu-1 (CD5) plus complement. When this treatment was done on day 8 of IL-2 cocultivation, anti Leu-11 plus complement suppressed cytotoxicity significantly, and anti Leu-1 plus complement also induced mild suppression. The phenotypic characteristics of cells revealed the significant increase of anti Leu-19+ cells in IL-2 stimulated day 8 cells. High density fractions of Percoll gradient contained mostly T lymphocytes and showed no cytotoxicity against autologous tumor cells. However, cocultivation with IL-2 for 8 days induced the cytotoxicity, associated with increased number of anti Leu-19+ cells. These results suggested that IL-2 induced cytotoxic activity against autologous tumor cells might be related to the increase of anti Leu-19+ cells.

摘要

外周血单个核细胞经Percoll密度梯度离心后的低密度组分中含有大多数大颗粒淋巴细胞(LGL)。LGL被用于对20例血液系统恶性肿瘤患者(9例急性髓系白血病、4例急性淋巴细胞白血病和7例非霍奇金淋巴瘤)的自体肿瘤细胞进行5小时的51Cr释放细胞毒性测定。平均细胞毒性百分比(% CTX)为6.0%,培养基中添加干扰素-β(IFN-β)和白细胞介素-2(IL-2)后,% CTX分别显著增加至15.0%和26.1%。当对在含有IFN-β和IL-2的培养基中培养的LGL进行为期8天的每日细胞毒性评估时,IFN-β对% CTX的增强作用在数天内下降,而IL-2的增强作用持续超过8天。用抗Leu-11(CD16)加补体预处理LGL可消除IFN-β或IL-2的增强作用,但抗Leu-1(CD5)加补体则不能。当在IL-2共培养的第8天进行这种处理时,抗Leu-11加补体显著抑制细胞毒性,抗Leu-1加补体也诱导轻度抑制。细胞的表型特征显示,在IL-2刺激的第8天细胞中,抗Leu-19+细胞显著增加。Percoll梯度的高密度组分主要含有T淋巴细胞,对自体肿瘤细胞无细胞毒性。然而,与IL-2共培养8天可诱导细胞毒性,同时抗Leu-19+细胞数量增加。这些结果表明,IL-2诱导的针对自体肿瘤细胞的细胞毒性活性可能与抗Leu-19+细胞的增加有关。

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