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SCOR in Pathobiology of Fibrotic Lung Disease

SCOR in Pathobiology of Fibrotic Lung Disease
SCOR 在纤维化肺疾病病理学中的应用
批准号:
6998978
负责人:
Galen B Toews
金额:
$189.36万
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:
2001-12-26 至 2006-11-30

项目摘要

项目成果

Galen B Toews的其他基金

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中文摘要
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英文摘要
(Applicant's Abstract) The long-term objective of this SCOR is to further our understanding of the pathogenesis of the idiopathic interstitial pneumonias (UP). A clear understanding of the pathogenesis of these diseases is required to develop new treatment strategies. The central hypothesis for this SCOR proposal is: Local alterations in the elaboration of effector molecules or in the expression of receptors by inflammatory, epithelial, and mesenchymal cells create an alveolar microenvironment that favors the fibroproliferative response rather than normal repair. Such dysregulation in autocrine and/or paracrine regulatory loops determine susceptibility to and expression of fibrotic lung disease. In each project of this SCOR, this central hypothesis will be extended to define the role of a specific set of mediators and/or receptors in pathobiological processes relevant to fibrogenesis. These mediators include cytokines, chemokines, elcosanoids and proteases. Studies will utilize animal models of fibrosis and/or patients with HP to examine abnormalities in cells and tissues and the role of each mediator in the pathobiology of fibrosis. An important feature is the mechanistic insights these studies provide to the use of standard (prednisone, azathioprine + prednisone) and novel (5-lipoxygenase inhibitor, zileuton) therapeutic agents under investigation in our ongoing clinical project. This SCOR will take a multi-disciplinary approach to testing these hypotheses. The expertise of investigators trained in Internal Medicine, Pathology, Cell and Molecular Biology, Biochemistry, and Biostatistics will be utilized. The strength of this proposal are the investigators long-standing interests in fibrotic lung disease, a proven commitment to collaborative research by both clinicians and basic scientists, access to a large population of IIP patients, and extraordinary institutional resources of biomedical Research. This SCOR capitalizes on a bench to bedside continuum of research that is crucial to translate advances in basic research to the clinical arena.
期刊论文(41)
专著(0)
科研奖励(0)
会议论文
Inducible lung-specific urokinase expression reduces fibrosis and mortality after lung injury in mice.
诱导性肺特异性尿激酶表达可减少小鼠肺损伤后的纤维化和死亡率。
DOI: 10.1152/ajplung.00049.2002
发表时间: 2002
期刊: American journal of physiology. Lung cellular and molecular physiology
影响因子: --
作者: [Sisson,ThomasH, Hanson,KerstinE, Subbotina,Natalya, Patwardhan,Anjali, Hattori,Noboru, Simon,RichardH]
通讯作者: Simon,RichardH
DOI: 10.1513/pats.200602-022tk
发表时间: 2006-06-01
期刊: Proceedings of the American Thoracic Society
影响因子: --
作者: [Martinez, Fernando J, Flaherty, Kevin]
通讯作者: Flaherty, Kevin
DOI: 10.1126/scitranslmed.3001510
发表时间: 2010-11-10
期刊: Science translational medicine
影响因子: 17.1
作者: [Trujillo G, Meneghin A, Flaherty KR, Sholl LM, Myers JL, Kazerooni EA, Gross BH, Oak SR, Coelho AL, Evanoff H, Day E, Toews GB, Joshi AD, Schaller MA, Waters B, Jarai G, Westwick J, Kunkel SL, Martinez FJ, Hogaboam CM]
通讯作者: Hogaboam CM
Nonspecific interstitial pneumonia.
非特异性间质性肺炎。
DOI: 10.1016/j.ccm.2011.11.003
发表时间: 2012
期刊: Clinics in chest medicine
影响因子: 5.7
作者: [Kinder,BrentWayne]
通讯作者: Kinder,BrentWayne
6
    Herpesvirus infection/injury govern fibrocyte recruitment and activation
    Herpesvirus infection/injury govern fibrocyte recruitment and activation
    Herpesvirus infection/injury govern fibrocyte recruitment and activation
    Regulation of fibrosis by alveolar cells expressing CCR2