CD8+ T cell trafficking to the normal lung
CD8+ T cell trafficking to the normal lung
批准号:
7204196
负责人:
Thomas J Braciale
金额:
$36.15万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-04-01 至 2009-03-31
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): This project is designed to investigate the trafficking of CD8+ T-lymphocytes to the pulmonary microcirculation (alveolar capillaries) and the associated interstitial tissue/airways of the normal (noninflamed) murine lungs. Our long-term objective is to understand, in molecular terms, the factors which regulate activated CD8+ T-cell migration to the pulmonary microcirculation, the retention of those cells at the site, and the subsequent egress of the cells from the vascular compartment into the lung interstitium. It is based on our emerging evidence suggesting that activated CD8+ T-cells are retained in the normal lung environment, because they constitutively egress from the pulmonary circulation vascular compartment (i.e., alveolar capillaries) into the interstitium of the normal/non-inflamed lungs. Our data further suggests that prolonged T-cell retention and egress into the lung interstitium may be mediated by specific adhesive receptor/ligand interactions, and may be dependent on a chemokine-dependent homing/retention mechanism. To further explore this process of activated CD8+ T-cell homing/retention in the normal lungs, we propose the following Specific Aims: 1. To characterize the trafficking of naive (resting) and activated CD8+ T lymphocytes to the normal (non-inflamed) pulmonary microcirculation, and the egress of these cells into the alveolar interstitium; 2. To analyze the mechanism by which activated CD8+ T-cells home to the pulmonary micro capillary bed and egress into the interstitium of the normal lung. We will employ a variety of strategies including cell and whole animal imaging techniques to examine the retention and compartmentalization of transferred CD8+ T-cells within the normal lungs. The proposed analysis should provide new information on the factors controlling the interaction of T-lymphocytes with the pulmonary microcirculation and the associated interstitium/airways, as well as, on the underlying mechanism controlling this process.
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Immune Regulation of Virus Clearance and Tissue Injury at Sites of Infection
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财政年份:2009
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Immune Regulation of Virus Clearance and Tissue Injury at Sites of Infection
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批准号:8282813
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Administration
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资助金额:$12.65万
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Immune Regulation of Virus Clearance and Tissue Injury at Sites of Infection
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资助金额:$157.24万
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财政年份:2009
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依托单位:
CD8+ T cell trafficking to the normal lung
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批准号:6725653
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项目类别:
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资助金额:$34.2万
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财政年份:2004
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负责人:Thomas J Braciale
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依托单位:
CD8+ T cell trafficking to the normal lung
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项目类别:
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资助金额:$37.23万
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财政年份:2004
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负责人:Thomas J Braciale
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依托单位:
CD8+ T cell trafficking to the normal lung
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批准号:6875017
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项目类别:
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资助金额:$38.05万
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财政年份:2004
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负责人:Thomas J Braciale
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依托单位:
RESPIRATORY SYNCYTIAL VIRUS AND ATOPIC PULMONARY RESPONSE
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批准号:6345923
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项目类别:
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资助金额:$19.31万
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财政年份:2000
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负责人:Thomas J Braciale
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依托单位:
RESPIRATORY SYNCYTIAL VIRUS AND ATOPIC PULMONARY RESPONSE
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批准号:6201176
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项目类别:
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资助金额:$19.31万
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财政年份:1999
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负责人:Thomas J Braciale
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依托单位:
RESPIRATORY SYNCYTIAL VIRUS AND ATOPIC PULMONARY RESPONSE
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批准号:6099672
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项目类别:
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资助金额:$19.31万
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财政年份:1998
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负责人:Thomas J Braciale
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依托单位:
RESPIRATORY SYNCYTIAL VIRUS AND ATOPIC PULMONARY RESPONSE
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批准号:6235144
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项目类别:
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资助金额:$18.75万
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负责人:Thomas J Braciale
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依托单位:
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGY
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批准号:6372824
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项目类别:
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资助金额:$31.1万
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财政年份:1995
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负责人:Thomas J Braciale
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依托单位:
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGY
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项目类别:
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资助金额:$28.67万
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财政年份:1995
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负责人:Thomas J Braciale
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依托单位:
国内基金
海外基金
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