课题基金 / 基金详情

Administrative Core

Administrative Core
行政核心
批准号:
8234069
负责人:
JAY A NELSON
金额:
$57.09万
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:
2011-03-01 至 2014-02-28

项目摘要

项目成果

JAY A NELSON的其他基金

相似基金

相关文献

中文摘要
翻译
太平洋西北地区生物防御和新兴传染病卓越中心 疾病研究(PNWRCE)汇集了一个具有广泛专业知识的研究人员联盟, 针对广泛的NIAID A-C类优先病原体的基础和转化研究能力。 我们的研究活动旨在更深入地了解病原体-宿主相互作用;如何 这些相互作用影响先天性和适应性免疫应答;以及与年龄相关的免疫缺陷, 导致免疫衰老和对传染病易感性增加。生成的信息 这些活动将促进下一代治疗、诊断和疫苗的开发 对抗A-C类病原体PNWRCE还将培训年轻的生物防御研究人员, 新兴传染病研究,促进新的研究计划的发展,并提供设施 在国家生物防御或新出现的传染性疾病发生时, 疾病紧急 研究主题 该方案的研究活动由两个不同但相互关联的主题统一起来: 识别免疫系统中与年龄相关的缺陷,以促进 疫苗和补充疗法 和 利用系统生物学和系统遗传学方法确定病原体-宿主相互作用 以及先天免疫和适应性免疫的机制 这些主题反映了PNWRCE调查人员的优势,并旨在解决重大的 公共卫生需求和当前RCE计划中的差距。特别是,我们使用系统级方法 我们对先天性和适应性免疫以及免疫衰老的关注为识别 治疗干预和增强目前疫苗战略的目标。此外,我们的研究 这些活动旨在将这些福利扩大到包括老年人在内的弱势群体, 美国社会中增长最快的部分。我们对病原体-宿主相互作用的宿主方面的关注将 使我们能够发现新的抗病毒产品的细胞靶点, 通过病原体突变,更有可能产生广谱作用。如NIAID所述 生物防御研究战略计划(2007年更新),广谱药物的开发,特别是 抗病毒药物是NIAID的首要任务我们亦鼓励发展广泛的平台,并会 建立并提供一个创新的小鼠系统遗传学平台,可用于识别宿主 对多种病原体的易感性等位基因。广谱战略认识到, 生物威胁和对反应更快的生物防御能力的需求。在这方面,有一个紧迫的 我们需要针对许多A-C类病原体的疫苗,我们的研究将提高疫苗 发展战略,并提供新的方法,通过早期评估疫苗的效力, 鉴定免疫的基因组相关物。
英文摘要
The proposed Pacific Northwest Regional Center of Excellence for Biodefense and Emerging Infectious Diseases Research (PNWRCE) brings together a consortium of investigators with extensive expertise and basic and translational research capacity directed at a broad range of NIAID Category A-C Priority Pathogens. Our research activities are aimed at providing a deeper understanding of pathogen-host interactions; how these interactions impact innate and adaptive immune responses; and the age-related defects in immunity that lead to immunosenescence and an increased vulnerability to infectious disease. The information generated from these activities will facilitate the development of next-generation therapeutics, diagnostics, and vaccines against Category A-C Pathogens. The PNWRCE will also train young investigators for biodefense and emerging infectious disease research, foster the development of new research programs, and provide facilities and scientific support to first-line responders in the event of a national biodefense or emerging infectious disease emergency. RESEARCH THEMES The research activities of the PNWRCE are unified by two distinct but interrelated themes: The identification of age-related defects in the immune system to facilitate the development of vaccines and supplemental therapies and The use of systems biology and systems genetics approaches to define pathogen-host interactions and mechanisms of innate and adaptive immunity These themes reflect the strengths of PNWRCE investigators and are geared toward addressing significant public health needs and gaps in the current RCE program. In particular, our use of systems-level approaches and our focus on innate and adaptive immunity and immunosenescence provide new opportunities to identify targets for therapeutic intervention and enhancements to current vaccine strategies. Moreover, our research activities are designed to extend these benefits to vulnerable populations, including the aged, which represents the fastest growing segment of American society. Our focus on the host side of pathogen-host interactions will allow us to discover new cellular targets for antiviral products that are less likely to be sensitive to escape through pathogen mutation and more likely to have a broad spectrum of action. As outlined in the NIAID Strategic Plan for Biodefense Research (2007 Update), the development of broad-spectrum drugs, particularly antivirals, is an NIAID priority. The development of broad-spectrum platforms is also encouraged, and we will generate and make available an innovative mouse systems genetics platform that can be used to identify host susceptibility alleles to a variety of pathogens. The broad-spectrum strategy recognizes the expanding range of biological threats and the need for a more responsive biodefense capability. In this regard, there is a pressing need for vaccines against many Category A-C Pathogens, and our research will enhance vaccine development strategies as well as provide new methods for the early evaluation of vaccine efficacy through the identification of genomic correlates of immunity.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
International Herpesvirus Workshop
The Administrative Core
Human Cytomegalovirus dysregulation of host hematopoietic progenitor cell signaling pathways to modulate latency and reactivation
海外基金