Estep Ryan D, Rawlings Stephanie D, Li Helen, Manoharan Minsha, Blaine Elizabeth T, O'Connor Megan A, Messaoudi Ilhem, Axthelm Michael K, Wong Scott W
Vaccine and Gene Therapy Institute, Oregon Health and Science University, Beaverton, Oregon, USA.
School of Medicine, University of California, Riverside, Riverside, California, USA.
J Virol. 2014 Sep;88(18):10635-54. doi: 10.1128/JVI.01276-14. Epub 2014 Jul 2.
Rhesus macaque rhadinovirus (RRV) is a gammaherpesvirus of rhesus macaque (RM) monkeys that is closely related to human herpesvirus 8 (HHV-8)/Kaposi's Sarcoma-associated herpesvirus (KSHV), and it is capable of inducing diseases in simian immunodeficiency virus (SIV)-infected RM that are similar to those seen in humans coinfected with HIV and HHV-8. Both HHV-8 and RRV encode viral CD200 (vCD200) molecules that are homologues of cellular CD200, a membrane glycoprotein that regulates immune responses and helps maintain immune homeostasis via interactions with the CD200 receptor (CD200R). Though the functions of RRV and HHV-8 vCD200 molecules have been examined in vitro, the precise roles that these viral proteins play during in vivo infection remain unknown. Thus, to address the contributions of RRV vCD200 to immune regulation and disease in vivo, we generated a form of RRV that lacked expression of vCD200 for use in infection studies in RM. Our data indicated that RRV vCD200 expression limits immune responses against RRV at early times postinfection and also impacts viral loads, but it does not appear to have significant effects on disease development. Further, examination of the distribution pattern of CD200R in RM indicated that this receptor is expressed on a majority of cells in peripheral blood mononuclear cells, including B and T cells, suggesting potentially wider regulatory capabilities for both vCD200 and CD200 that are not strictly limited to myeloid lineage cells. In addition, we also demonstrate that RRV infection affects CD200R expression levels in vivo, although vCD200 expression does not play a role in this phenomenon.
Cellular CD200 and its receptor, CD200R, compose a pathway that is important in regulating immune responses and is known to play a role in a variety of human diseases. A number of pathogens have been found to modulate the CD200-CD200R pathway during infection, including human herpesvirus 8 (HHV-8), the causative agent of Kaposi's sarcoma and B cell neoplasms in AIDS patients, and a closely related primate virus, rhesus macaque rhadinovirus (RRV), which infects and induces disease in rhesus macaque monkeys. HHV-8 and RRV encode homologues of CD200, termed vCD200, which are thought to play a role in preventing immune responses against these viruses. However, neither molecule has been studied in an in vivo model of infection to address their actual contributions to immunoregulation and disease. Here we report findings from our studies in which we analyzed the properties of a mutant form of RRV that lacks vCD200 expression in infected rhesus macaques.
恒河猴疱疹病毒(RRV)是恒河猴(RM)的一种γ疱疹病毒,与人类疱疹病毒8型(HHV - 8)/卡波西肉瘤相关疱疹病毒(KSHV)密切相关,它能够在感染猿猴免疫缺陷病毒(SIV)的恒河猴中引发疾病,这些疾病与同时感染HIV和HHV - 8的人类所患疾病相似。HHV - 8和RRV都编码病毒CD200(vCD200)分子,它们是细胞CD200的同源物,细胞CD200是一种膜糖蛋白,通过与CD200受体(CD200R)相互作用来调节免疫反应并维持免疫稳态。尽管已经在体外研究了RRV和HHV - 8 vCD200分子的功能,但这些病毒蛋白在体内感染过程中的确切作用仍然未知。因此,为了研究RRV vCD200对体内免疫调节和疾病的作用,我们构建了一种缺乏vCD200表达的RRV,用于恒河猴的感染研究。我们的数据表明,RRV vCD200的表达在感染后早期限制了针对RRV的免疫反应,也影响病毒载量,但似乎对疾病发展没有显著影响。此外,对恒河猴中CD200R分布模式的研究表明,该受体在外周血单个核细胞的大多数细胞上表达,包括B细胞和T细胞,这表明vCD200和CD200可能具有更广泛的调节能力,并不严格局限于髓系细胞。此外,我们还证明RRV感染会影响体内CD200R的表达水平,尽管vCD200的表达在这一现象中不起作用。
细胞CD200及其受体CD200R构成了一条在调节免疫反应中很重要的途径,并且已知在多种人类疾病中发挥作用。已经发现许多病原体在感染过程中会调节CD200 - CD200R途径,包括卡波西肉瘤和艾滋病患者B细胞肿瘤的病原体人类疱疹病毒8型(HHV - 8),以及一种密切相关的灵长类病毒恒河猴疱疹病毒(RRV),它感染恒河猴并引发疾病。HHV - 8和RRV编码CD200的同源物,称为vCD200,它们被认为在防止针对这些病毒的免疫反应中发挥作用。然而,尚未在体内感染模型中对这两种分子进行研究以确定它们对免疫调节和疾病的实际作用。在这里,我们报告了我们的研究结果,其中我们分析了在感染的恒河猴中缺乏vCD200表达的RRV突变体的特性。