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重组人白细胞介素2增强人天然细胞介导的细胞毒性作用。

Augmentation of human natural cell-mediated cytotoxicity by recombinant human interleukin 2.

作者信息

Svedersky L P, Shepard H M, Spencer S A, Shalaby M R, Palladino M A

出版信息

J Immunol. 1984 Aug;133(2):714-8.

PMID:6203975
Abstract

Human peripheral blood mononuclear cells (PBMC) demonstrated increased natural cell-mediated cytotoxicity (NCMC) activity after only 5 min of exposure to purified recombinant human IL 2 or interferon (IFN)-gamma. The mechanism of NCMC augmentation by treatment with IL 2 is not entirely dependent on IFN-gamma production because: a) IL 2 was found to augment NCMC activity at levels which did not induce detectable IFN-gamma; b) IL 2 required only 5 min of exposure to PBMC to augment NCMC activity, whereas 3 hr of contact were required to demonstrate detectable IFN-gamma levels; c) the levels of NCMC enhancement by treatment with IL 2 exceeded the amount of NCMC enhancement that could be due to IFN alone; d) anti-recombinant IFN-gamma, which totally eliminated the augmentation of NCMC enhancement by IFN-gamma, only partially reduced the augmentation of NCMC activity by IL 2; and e) combination treatment of PBMC with IL 2 and IFN-gamma resulted in a synergistic enhancement of NCMC. The results strongly support the conclusion that augmentation of NCMC by IL 2 and IFN-gamma involve overlapping mechanisms.

摘要

人类外周血单个核细胞(PBMC)在仅暴露于纯化的重组人白细胞介素2(IL 2)或干扰素(IFN)-γ 5分钟后,其天然细胞介导的细胞毒性(NCMC)活性就有所增强。用IL 2处理增强NCMC的机制并不完全依赖于IFN-γ的产生,原因如下:a)发现IL 2在未诱导可检测到的IFN-γ的水平下就能增强NCMC活性;b)IL 2仅需与PBMC接触5分钟就能增强NCMC活性,而显示可检测到的IFN-γ水平则需要3小时的接触时间;c)用IL 2处理后NCMC增强的水平超过了仅由IFN引起的NCMC增强量;d)抗重组IFN-γ完全消除了IFN-γ对NCMC增强的作用,但仅部分降低了IL 2对NCMC活性的增强作用;e)PBMC与IL 2和IFN-γ联合处理导致NCMC协同增强。这些结果有力地支持了以下结论:IL 2和IFN-γ增强NCMC涉及重叠机制。

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