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干扰素诱导肿瘤靶细胞对白细胞介素-2激活的杀伤细胞裂解产生抗性。

Interferon-induced resistance of tumor target cells against lysis by interleukin-2-activated killer cells.

作者信息

Takagi S, Minakuchi J, Okawa H, Yata J

机构信息

Department of Pediatrics, Tokyo Medical and Dental University.

出版信息

Tohoku J Exp Med. 1989 Feb;157(2):131-6. doi: 10.1620/tjem.157.131.

Abstract

IFN-gamma has been shown to decrease the susceptibility of target cells to NK cell-mediated cytotoxicity. In this report, the effect of IFN-gamma on the sensitivity of target cells to killing by various human lymphocyte cytotoxic activities such as NK/K, IL-2-augmented NK/K cell activity, and IL-2-activated killer activity were studied. Although NK-sensitive K562 cells showed marked resistance to NK cell activity as previously reported, the resistance was overwhelmed by augmentation of NK activity with IL-2. IL-2-activated killer cell activity, which can lyse NK-resistant tumor cell lines upon culture in IL-2, showed decreased cytotoxicity against most of the IFN-gamma-treated target cells tested. By contrast, no decrease of target cell sensitivity to K cells was observed, even though K cells were treated with IL-2. These findings suggest that as far as NK-resistant tumor cells are concerned, an IFN-dependent mechanism inhibits the Fc receptor-independent mediators of tumor surveillance, but not Fc receptor-dependent ones. This should be considered when planning adoptive immunotherapy of IL-2-activated killer cells for human malignancy.

摘要

γ干扰素已被证明可降低靶细胞对自然杀伤细胞介导的细胞毒性的敏感性。在本报告中,研究了γ干扰素对靶细胞对各种人类淋巴细胞细胞毒性活性(如NK/K、IL-2增强的NK/K细胞活性和IL-2激活的杀伤活性)杀伤敏感性的影响。尽管如先前报道,对NK敏感的K562细胞对NK细胞活性表现出明显抗性,但用IL-2增强NK活性后这种抗性被克服。IL-2激活的杀伤细胞活性在IL-2中培养时可裂解对NK有抗性的肿瘤细胞系,但对大多数经γ干扰素处理的测试靶细胞的细胞毒性降低。相比之下,即使K细胞用IL-2处理,也未观察到靶细胞对K细胞敏感性的降低。这些发现表明,就对NK有抗性的肿瘤细胞而言,一种依赖干扰素的机制抑制肿瘤监视的不依赖Fc受体的介质,但不抑制依赖Fc受体的介质。在计划对人类恶性肿瘤采用IL-2激活的杀伤细胞进行过继性免疫治疗时应考虑到这一点。

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