The alpha chemokine, interleukin 8, inhibits the antiviral action of interferon alpha

被引:112
作者
Khabar, KSA
AlZoghaibi, F
AlAhdal, MN
Murayama, T
Dhalla, M
Mukaida, N
Taha, M
AlSedairy, ST
Siddiqui, Y
Kessie, G
Matsushima, K
机构
[1] KANAZAWA MED UNIV,DEPT MICROBIOL,KANAZAWA,ISHIKAWA 9200,JAPAN
[2] KANAZAWA UNIV,DEPT PHARMACOL,KANAZAWA,ISHIKAWA 920,JAPAN
[3] UNIV TOKYO,DEPT MOL PREVENT MED,TOKYO 113,JAPAN
关键词
D O I
10.1084/jem.186.7.1077
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interferon (IFN) exhibits a potent antiviral activity in vitro and plays a major role in the early defense against viruses. Like IFN, the proinflammatory chemokine, interleukin (IL)-8, is induced by viruses and appears in circulation during viral infections. In an in vitro cytopathic effect assay for IFN, we found that IL-8 can inhibit IFN-alpha activity in a dose-dependent manner. This action was reversed by specific monoclonal antibodies to IL-8. The chemokine was able to attenuate the IFN-mediated inhibition of viral replication as determined by measuring infectious virus yield. IL-8 also diminished the ability of IFN to inhibit an early stage of viral replication since IL-8 attenuated the inhibition of the formation of viral proteins, It appeared that IL-8 interfered with a late rather than an early step of IFN-mediated pathway such as early gene expression. The IL-8 inhibitory action on IFN-alpha antiviral activity was associated with reduced 2',5'-A oligoadenylate synthetase activity, a pathway well correlative with the anti-encephalomyocarditis virus action of IFN-alpha. Understanding pathways that antagonize IFN action may lead to novel approaches to potentiate endogenous and therapeutic IFN.
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收藏
页码:1077 / 1085
页数:9
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