EVASION OF ANTIGEN PRESENTATION BY RHESUS CYTOMEGALOVIRUS

恒河猴巨细胞病毒逃避抗原呈递

• 批准号: 7958445
• 负责人: Klaus J Fruh
• 金额: $ 8.03万
• 依托单位: OREGON HEALTH & SCIENCE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-08-04 至 2010-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7958445
• 关键词: Anabolism; Antigen Presentation; CD8B1 gene; Cells; Computer Retrieval of Information on Scientific Projects Database; Cytomegalovirus; Family; Funding; Genes; Genome; Glycoproteins; Goals; Grant; Homologous Gene; Immune; Immunomodulators; In Vitro; Infection; Institution; Intercept; Laboratories; Light; Macaca mulatta; Maintenance; Modeling; Molecular; Open Reading Frames; Phenotype; Primates; Research; Research Personnel; Resources; Role; Source; T-Lymphocyte; United States National Institutes of Health; Viral Genes; Work; in vivo; novel

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The major goal is to identify and characterize cytomegaloviral immunomodulatory functions in vitro and to define their role for immune evasion in vivo. Work in several laboratories, including ours, previously uncovered that four glycoproteins of the US6-family (US2, US3, US6 and US11) inhibit assembly and transport of MHC I in HCMV-infected cells. We demonstrated that RhCMV encodes functional homologues for each of these four immunomodulators, (Rh182, Rh184, Rh185 and Rh189). Additionally, we made the unexpected discovery that RhCMV encodes a novel mechanism which intercepts biosynthesis of MHC I heavy chains (HC), but not light chains (beta2m). The goals of this application are a) to examine whether MHC I interference mechanisms are important for evading CD8+ T cell control in vivo, b) to examine the importance of US6-related and -unrelated genes in immune evasion in vivo and c) to characterize the molecular mechanism of VIHCE. Specific Aim 1: Identification of the gene encoding VIHCE. The goal of this specific aim is to identify which open reading frame in the RhCMV genome encodes the gene responsible for the VIHCE phenotype. Specific Aim 2: Functional characterization of VIHCE. The goal of this specific aim is to further characterize the VIHCE mechanism in cells infected with wildtype or VIHCE-deleted RhCMV. Specific Aim 3: The role of MHC I modulators for establishment and maintenance of persistent infection by RhCMV. We will examine the role of VIHCE and US6-related genes for viral immune evasion in a re-infection model in rhesus macaques.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 主要目的是确定和表征巨细胞病毒的免疫调节功能在体外，并确定其在体内免疫逃逸的作用。包括我们在内的几个实验室的工作先前发现，US 6家族的四种糖蛋白（US 2，US 3，US 6和US 11）抑制HCMV感染细胞中MHC I的组装和转运。我们证明了RhCMV编码这四种免疫调节剂（Rh 182、Rh 184、Rh 185和Rh 189）中每一种的功能同源物。此外，我们意外地发现，RhCMV编码一种新的机制，该机制拦截MHC I重链（HC）的生物合成，但不拦截轻链（β 2 m）。本申请的目的是a）检查MHC I干扰机制对于逃避体内CD 8 + T细胞控制是否重要，B）检查US 6相关和不相关基因在体内免疫逃避中的重要性和c）表征VIHCE的分子机制。 具体目的1：鉴定编码VIHCE的基因。该特定目的的目标是鉴定RhCMV基因组中哪个开放阅读框编码负责VIHCE表型的基因。 具体目标2：VIHCE的功能表征。该特定目的的目标是进一步表征在用野生型或VIHCE缺失的RhCMV感染的细胞中的VIHCE机制。 具体目标3：MHC I调节剂在建立和维持RhCMV持续感染中的作用。我们将研究恒河猴再感染模型中VIHCE和US 6相关基因对病毒免疫逃避的作用。