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干扰素调节的Mx基因对白介素-1、肿瘤坏死因子及其他细胞因子无反应。

Interferon-regulated Mx genes are not responsive to interleukin-1, tumor necrosis factor, and other cytokines.

作者信息

Simon A, Fäh J, Haller O, Staeheli P

机构信息

Institut für Immunologie und Virologie, Universität Zürich, Switzerland.

出版信息

J Virol. 1991 Feb;65(2):968-71. doi: 10.1128/JVI.65.2.968-971.1991.

Abstract

Accumulation of Mx gene products in cells of patients and experimental animals has been recognized as a useful marker for detecting minute quantities of biologically active interferon (IFN). Goetschy et al. (J. Goetschy, H. Zeller, J. Content, and M. A. Horisberger, J. Virol. 63:2616-2622, 1989) reported that not only IFNs but also interleukin-1 (IL-1) and tumor necrosis factor (TNF) were potent inducers of the human Mx genes. However, we observed no Mx induction in cultured human fibroblasts or in human peripheral blood mononuclear cells treated with various concentrations of IL-1 alpha or TNF-alpha. Mx induction was found in the spleens of mice treated with TNF-alpha or IL-1 alpha, but this effect could be neutralized with antibodies to murine IFN-alpha/beta. Of the other cytokines that we tested (IL-2, IL-6, and granulocyte-macrophage colony-stimulating factor), only IL-2 induced the Mx genes in peripheral blood mononuclear cells, but antibodies to human IFN-beta efficiently neutralized this effect. Our results thus indicate that IFNs are the only cytokines with intrinsic Mx-inducing activity.

摘要

患者和实验动物细胞中Mx基因产物的积累已被认为是检测微量生物活性干扰素(IFN)的有用标志物。戈奇等人(J. 戈奇、H. 泽勒、J. 孔唐和M. A. 霍里斯贝格尔,《病毒学杂志》63:2616 - 2622,1989年)报告称,不仅IFN,而且白细胞介素-1(IL-1)和肿瘤坏死因子(TNF)都是人类Mx基因的有效诱导剂。然而,我们在用不同浓度的IL-1α或TNF-α处理的培养人成纤维细胞或人外周血单个核细胞中未观察到Mx诱导。在用TNF-α或IL-1α处理的小鼠脾脏中发现了Mx诱导,但这种效应可用抗小鼠IFN-α/β抗体中和。在我们测试的其他细胞因子(IL-2、IL-6和粒细胞-巨噬细胞集落刺激因子)中,只有IL-2能在外周血单个核细胞中诱导Mx基因,但抗人IFN-β抗体能有效中和这种效应。因此,我们的结果表明,IFN是唯一具有内在Mx诱导活性的细胞因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9f2/239840/4a7de02d839b/jvirol00045-0423-a.jpg

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