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COLUMBIA UNIVERSITY ASTHMA AND ALLERGY CLINICAL RESEARCH

COLUMBIA UNIVERSITY ASTHMA AND ALLERGY CLINICAL RESEARCH
哥伦比亚大学哮喘和过敏临床研究
批准号:
6751921
负责人:
CHRISTIAN W SCHINDLER
金额:
$152.01万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-08-27 至 2006-05-31
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项目摘要

项目成果

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中文摘要
翻译
总体描述(由申请人提供):特应性哮喘和其他过敏性疾病 疾病是由个体对环境的病理反应引起的。 抗原。要治愈这些疾病,需要了解 启动这些免疫反应所需的机制和 传播它们所需的机制。最近的主要范式之一 这一领域的研究已经产生了启蒙和 过敏性免疫反应的传播需要不同的 炎性细胞。此外,这种交互需要交换 这些细胞之间的信息。信息交流的核心 参与过敏免疫反应的细胞之间使用的是信号 将这些信号传递到细胞核的途径。这 认识到这一点已经开始推动治疗研究朝着 改变这些信号通路以改变由此产生的过敏反应 免疫反应。本研究中心试图了解 过敏和哮喘免疫反应中的信号通路。在项目1中, 辛德勒博士建议研究STAT信号在发育中的作用 和树突状细胞(DC)的功能。在项目2中,佩尼斯博士将研究 CD23在正常人和过敏者中的调节。在项目3中,克莱恩斯博士 我将研究Fc受体在Fc受体启动和繁殖中的作用 过敏和哮喘免疫反应。在项目4中,罗斯曼博士将研究 Pim激酶如何改变IL-4信号及其如何改变过敏性免疫 回应。在项目5中,米勒博士将研究 未出世的孩子。通过该中心获得的知识将提高我们的 了解过敏性免疫所需的信号通路 回应。一个科学核心和一个管理核心将支持这些 项目。科学核心将提供技术专门知识和援助 在哮喘和过敏免疫反应的小鼠模型中。行政部门 CORE将协助组织S中心的活动。
英文摘要
OVERALL DESCRIPTION (provided by applicant): Atopic asthma and other allergic diseases are caused by a pathologic response of individuals to environmental antigens. To cure these diseases will require an understanding of the mechanisms that are required to initiate these immune responses and the mechanisms required to propagate them. One of the major paradigms that recent research in this field has generated is that both the initiation and propagation of allergic immune responses requires the interaction of different inflammatory cells. In addition, this interaction requires the exchange of information between these cells. Central to the exchange of information between cells involved in an allergic immune response is the use of signaling pathways to transmit these signals to the nucleus of the cells. This realization has begun to drive therapeutic research in the direction of altering these signaling pathways in order to modify the resultant allergic immune response. This Research Center seeks to understand the role of signaling pathways in allergic and asthmatic immune responses. In Project 1, Dr. Schindler proposes to study the role of STAT signaling in the development and function of Dendritic Cells (DC). In Project 2, Dr. Pernis will study the regulation of CD23 in normal and allergic humans. In Project 3, Dr. Clynes will study the role of Fc receptors in the initiation and propagation of allergic and asthmatic immune responses. In Project 4, Dr. Rothman will study how Pim kinases alter IL-4 signaling and how this alters allergic immune responses. In Project 5, Dr. Miller will study the immune response of the unborn child. The knowledge gained by this Center will improve our understanding of the signaling pathways required for an allergic immune response. A Scientific Core and an Administrative Core will support these projects. The Scientific Core will provide technical expertise and assistance in murine models of asthma and allergic immune responses. The Administrative Core will assist in organizing the Center?s activities.
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会议论文
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