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OK-432介导白细胞介素1、白细胞介素2和γ干扰素的体外产生从而生成活化的杀伤样细胞。

Generation of activated killer-like cells by OK-432-mediated production of interleukin 1, interleukin 2, and interferon-gamma in vitro.

作者信息

Ujiie T

机构信息

Department of Experimental Therapeutics, Kanazawa University, Japan.

出版信息

Jpn J Exp Med. 1987 Dec;57(6):333-8.

PMID:3131563
Abstract

Human peripheral blood mononuclear (PBM) cells incubated for 3 or more days in medium containing streptococcal preparation OK-432 developed toxicity to natural killer-resistant tumor cell lines. The generation of cytotoxic cells by OK-432 was potentiated by exogenous lymphokines such as interleukin 2 (IL-2) and interferon-gamma (IFN-gamma), the former being much more effective than the latter, and was blocked by antibodies to these cytokines such as interleukin 1 (IL-1), IL-2, and IFN-gamma. Although monocyte-depleted PBM cells were barely responsive to OK-432, they gave rise to activated killer (AK) cells after being incubated in medium with both IL-2 and IFN-gamma. Their generation was augmented by exogenous IL-1 but not by OK-432. These data indicate that AK-like cells are generated from human PBM cells through mediation of IL-1, IL-2, and IFN-gamma produced by OK-432 in vitro.

摘要

在含有链球菌制剂OK-432的培养基中培养3天或更长时间的人外周血单个核(PBM)细胞,对自然杀伤抗性肿瘤细胞系产生了毒性。外源性淋巴因子如白细胞介素2(IL-2)和干扰素-γ(IFN-γ)可增强OK-432诱导细胞毒性细胞的生成,前者比后者更有效,并且这些细胞因子的抗体如白细胞介素1(IL-1)、IL-2和IFN-γ可阻断其生成。尽管单核细胞耗竭的PBM细胞对OK-432几乎无反应,但在含有IL-2和IFN-γ的培养基中培养后,它们可产生活化杀伤(AK)细胞。外源性IL-1可增强其生成,但OK-432不能。这些数据表明,在体外,OK-432产生的IL-1、IL-2和IFN-γ介导人PBM细胞产生了类似AK的细胞。

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