Westmoreland Susan V, Mansfield Keith G
Harvard Medical School, New England Primate Research Center, Southborough, MA, USA.
Comp Med. 2008 Feb;58(1):31-42.
With the emergence of the AIDS epidemic over the last 2 decades and the more recent identification of Kaposi sarcoma-associated herpesvirus (KSHV, Human herpesvirus 8), the genera of rhadinoviruses have gained importance as a family of viruses with oncogenic potential. First recognized in New World primates more than 30 y ago, the rhadinoviruses Saimiriine herpesvirus 2 and Ateline herpesvirus 2 have well-described transforming capabilities. Recently several new species-specific rhadinoviruses of Old World primates have been described, including retroperitoneal fibromatosis herpesvirus and rhesus rhadinovirus (Cercopithecine herpesvirus 17). Molecular analysis of these viruses has elucidated several functionally conserved genes and properties shared with KSHV involved in cellular proliferation, transformation, and immune evasion that facilitate the oncogenic potential of these viruses. This review examines the comparative pathobiology of KSHV, discusses the role of macaque rhadinoviruses as models of human disease, and outlines the derivation of specific pathogen-free animals.
在过去20年艾滋病流行以及最近卡波西肉瘤相关疱疹病毒(KSHV,人类疱疹病毒8型)被发现之后,嗜淋巴细胞性疱疹病毒属作为一类具有致癌潜力的病毒受到了更多关注。嗜淋巴细胞性疱疹病毒属的猴疱疹病毒2型和蛛猴疱疹病毒2型在30多年前首次在新大陆灵长类动物中被发现,它们具有明确的转化能力。最近,又发现了几种旧大陆灵长类动物的新的种特异性嗜淋巴细胞性疱疹病毒,包括腹膜后纤维瘤病疱疹病毒和恒河猴嗜淋巴细胞性疱疹病毒(猕猴疱疹病毒17型)。对这些病毒的分子分析揭示了一些功能保守的基因以及与KSHV共有的、参与细胞增殖、转化和免疫逃逸的特性,这些特性促进了这些病毒的致癌潜力。本文综述了KSHV的比较病理生物学,讨论了猕猴嗜淋巴细胞性疱疹病毒作为人类疾病模型的作用,并概述了无特定病原体动物的培育方法。