CELLULAR HOMOLOGS IN A NEW SIMIAN HERPESVIRUS
CELLULAR HOMOLOGS IN A NEW SIMIAN HERPESVIRUS
批准号:
8357585
负责人:
TIMOTHY M ROSE
金额:
$37.79万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-05-01 至 2012-04-30
关键词:
AIDS related cancerAIDS with Kaposi&aposs sarcomaAfrica South of the SaharaAnimal ModelCercopithecine Herpesvirus 1DevelopmentDiseaseEuropeFibromatosesFundingGrantHIVHerpesviridaeHerpesviridae InfectionsHomologous GeneHumanHuman Herpesvirus 8Immune responseImmunosuppressive AgentsInfectionKaposi SarcomaMacacaMalignant NeoplasmsNational Center for Research ResourcesPathogenesisPlayPopulation StudyPrimatesPrincipal InvestigatorResearchResearch InfrastructureResourcesRetroperitoneal SpaceRetroviridaeRoleSRV-2SourceUnited States National Institutes of HealthViruscosttransmission processtumor initiationtumorigenesis
中文摘要
这个子项目是利用资源的许多研究子项目之一。
由NIH/NCRR资助的中心拨款提供。对子项目的主要支持
子项目的首席调查员可能是由其他来源提供的,
包括美国国立卫生研究院的其他来源。为子项目列出的总成本可能
表示该子项目使用的中心基础设施的估计数量,
不是由NCRR赠款提供给次级项目或次级项目工作人员的直接资金。
艾滋病相关卡波西肉瘤(KS)是艾滋病相关的主要恶性肿瘤。人们认为,逆转录病毒HIV和疱疹病毒Kaposi肉瘤相关疱疹病毒(KSHV)之间的相互作用导致了疾病的发病。KSHV感染和KSHV相关恶性肿瘤是新出现的疾病,流行于地中海和撒哈拉以南非洲,但正在蔓延到美国和欧洲。SRV-2相关性腹膜后纤维瘤病(RF)与KSHV样疱疹病毒RFHVMn相关,是了解逆转录病毒和疱疹病毒在诱导肿瘤发生中相互作用的独特动物模型。了解这种动物模型中的病毒传播和肿瘤启动将提供关于人类和猕猴疾病的独特信息,这是开发KS治疗方法的基本前提。
在这个项目中,我们建议建立猕猴RFHV感染周期的基线参数。为了确定这种病毒是否在腹膜后纤维瘤病(RF)的发展中起作用,我们将描述它的感染周期以及SRV-2和其他免疫抑制剂对这些周期的干扰。我们将研究病毒传播和宿主对感染的反应。研究人群将包括感染RFHV的猕猴,包括活跃的、潜伏的或实验性感染的猕猴。
英文摘要
This subproject is one of many research subprojects utilizing the resources
provided by a Center grant funded by NIH/NCRR. Primary support for the subproject
and the subproject's principal investigator may have been provided by other sources,
including other NIH sources. The Total Cost listed for the subproject likely
represents the estimated amount of Center infrastructure utilized by the subproject,
not direct funding provided by the NCRR grant to the subproject or subproject staff.
AIDS-related Kaposi's sarcoma (KS) is the major AIDS-related malignancy. It is believed that an interaction between the retrovirus, HIV, and the herpesvirus, Kaposi's sarcoma-associated herpesvirus (KSHV), results in disease pathogenesis. KSHV-infection and KSHV-related malignancies are newly emerging diseases which are prevalent in the Mediterranean and Sub-Saharan Africa but are spreading into the U.S. and Europe. It is believed that SRV-2 related retroperitoneal fibromatosis (RF) which is associated with the KSHV-like herpesvirus, RFHVMn, is a unique animal model for understanding the interactions of retroviruses and herpesviruses in the induction of tumorigenesis. Understanding virus transmission and tumor initiation in this animal model would provide unique information concerning both the human and macaque diseases which is an essential prerequisite to developing treatments for KS.
In this project, we propose to establish the baseline parameters of the infectious cycle of the macaque RFHV. To determine if this virus plays a role in the development of retroperitoneal fibromatosis (RF) we will characterize its infectious cycles and the perturbation of these cycles by SRV-2 and other immunosuppressive agents. We will study virus transmission and the host response to infection. Study populations will include macaques with either active, latent or experimental infections with RFHV.
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CELLULAR HOMOLOGS IN A NEW SIMIAN HERPESVIRUS
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