Soluble interferon-gamma receptors encoded by poxviruses

被引:39
作者
Alcami, A
Smith, GL
机构
[1] Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, South Parks Road
基金
英国惠康基金; 英国医学研究理事会;
关键词
cytokine receptor; immune evasion; interferon; pathogenesis; poxvirus; vaccinia; virus evolution;
D O I
10.1016/0147-9571(96)00013-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Poxviruses encode a broad range of proteins that counteract the formidable attack of the immune response initiated in the host after infection, among which are proteins that mimic the extracellular binding domain of host cytokine receptors and are secreted from virus-infected cells. A soluble interferon-gamma receptor (IFN-gamma R) is produced early after infection and efficiently blocks the binding of IFN-gamma to cellular receptors, thus inhibiting both the anti-viral and immune functions of IFN-gamma. An IFN-gamma R is highly conserved among members of the poxvirus family, suggesting a major role in viral pathogenesis. The highly species-specific nature of the IFN system enables questions concerning the evolutionary relationship between poxviruses and their hosts to be addressed. The IFN-gamma R encoded by myxoma virus, a natural pathogen of rabbits, is specific for rabbit IFN-gamma. However, the IFN-gamma R encoded by orthopoxviruses (vaccinia, cowpox, camelpox, ectromelia) shows a novel, broad species specificity suggesting that these viruses have evolved in several species. The implications for the unknown origin and natural host(s) of vaccinia virus are discussed. Copyright (C) 1996 Elsevier Science Ltd.
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页码:305 / 317
页数:13
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