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FK-565和顺铂对淋巴因子(IL-2)激活的杀伤(LAK)细胞活性诱导的上调作用。

Up-regulation of induction of lymphokine (IL-2)-activated killer (LAK) cell activity by FK-565 and cisplatin.

作者信息

Basu S, Sodhi A, Singh S M, Suresh A

机构信息

School of Biotechnology, Banaras Hindu University, Varanasi, India.

出版信息

Immunol Lett. 1991 Mar;27(3):199-204. doi: 10.1016/0165-2478(91)90151-y.

Abstract

The role of cisplatin and FK-565 in up-regulation of lymphokine-activated killer (LAK) cell induction by IL-2 was examined. Treatment of blood mononuclear cells (MNC) of healthy donors with cisplatin or FK-565 in the presence of IL-2 resulted in a significant increase in LAK activity against natural killer (NK)-resistant Daudi cells as assessed by the 4 h 51Cr release assay. Blood MNC treated with cisplatin alone was not cytotoxic to Daudi cells. However, MNC treated with FK-565 showed some cytotoxicity against Daudi cells. Addition of cisplatin to IL-2-stimulated MNC did not increase proliferation but did enhance cytotoxicity. FK-565 together with IL-2 increased both proliferation and cytotoxicity of blood MNC. These data suggest the potential of cisplatin and FK-565 in LAK adoptive immunotherapy for cancer treatment.

摘要

研究了顺铂和FK-565在白细胞介素-2(IL-2)上调淋巴因子激活的杀伤细胞(LAK)诱导中的作用。在IL-2存在的情况下,用顺铂或FK-565处理健康供体的血液单核细胞(MNC),通过4小时51Cr释放试验评估,结果显示对天然杀伤(NK)抗性Daudi细胞的LAK活性显著增加。单独用顺铂处理的血液MNC对Daudi细胞无细胞毒性。然而,用FK-565处理的MNC对Daudi细胞表现出一定的细胞毒性。向IL-2刺激的MNC中添加顺铂不会增加增殖,但会增强细胞毒性。FK-565与IL-2一起增加了血液MNC的增殖和细胞毒性。这些数据表明顺铂和FK-565在LAK过继免疫疗法治疗癌症方面具有潜力。

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