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LYMPHOCYTIC ALVEOLITIS, IL 1B REGULATION AND LUNG INJURY

LYMPHOCYTIC ALVEOLITIS, IL 1B REGULATION AND LUNG INJURY
淋巴细胞性肺泡炎、IL 1B 调节和肺损伤
批准号:
2460082
负责人:
Mark Damian Wewers
金额:
$25.19万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1994
资助国家:
美国
项目状态:
已结题
起止时间:
1994-08-01 至 1999-07-31

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中文摘要
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英文摘要
DESCRIPTION (Adapted from the applicant's abstract) Several lines of evidence support the concept that important alterations in the pulmonary parenchyma occur in a substantial number of HIV- seropositive individuals prior to the development of recognized pulmonary complications. Although the pathogenesis of these abnormalities remains obscure, recent evidence has suggested an important role for an HIV-associated lymphocytic alveolitis and critical alveolar lymphocyte-alveolar macrophage interactions. The goal of the present project is to extend these observations by rigorously examining the significance of a lymphocytic alveolitis both with respect to physiologic and morphologic evidence of lung injury as well as with respect to dysregulation of cytokine production by alveolar macrophages. The following specific aims will be examined in an effort to reach this goal. Specific Aim 1 addresses this question: Is the in vivo presence of an HIV-associated lymphocytic alveolitis a critical determinant of parenchymal lung injury and proinflammatory cytokine upregulation? This aim will prospectively delineate the importance of a lymphocytic alveolitis with respect to physiologic, radiographic, and morphometric evidence of parenchymal lung damage as well as with respect to in vivo proinflammatory cytokine induction. The question in Specific Aim 2 addresses: Is the in vitro presence of alveolar cytoxic T- lymphocytes an important regulatory factor in the production of TNF alpha and IL-1 beta by alveolar macrophages? This aim will examine basic mechanisms of proinflammatory cytokine regulation and will focus primarily on the effects of CD8+ cytotoxic lymphocytes on IL-beta processing and release by alveolar macrophages. Because this study addresses the significance of one of the most common of the inflammatory events occurring in the alveolar environment in HIV, it may greatly advance knowledge of HIV- related lung disease. Perhaps more importantly, it focuses on the role of the alveolar lymphocyte as a central player in orchestrating pulmonary parenchymal damage through interactions with alveolar macrophages. As such, this project represents an opportunity to elucidate novel mechanisms of lung injury and to better understand factors of potentially fundamental importance to the regulation of inflammation.
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Regulation of lung host defense by inflammasome modifiers
  • 批准号:
    8048861
  • 项目类别:
  • 资助金额:
    $19.06万
  • 财政年份:
    2010
  • 负责人:
    Mark Damian Wewers
  • 依托单位:
Regulation of lung host defense by inflammasome modifiers
  • 批准号:
    8204686
  • 项目类别:
  • 资助金额:
    $22.88万
  • 财政年份:
    2010
  • 负责人:
    Mark Damian Wewers
  • 依托单位:
RIP2 caspase-1 signaling in macrophages
  • 批准号:
    7583471
  • 项目类别:
  • 资助金额:
    $37.5万
  • 财政年份:
    2009
  • 负责人:
    Mark Damian Wewers
  • 依托单位:
RIP2 caspase-1 signaling in macrophages
  • 批准号:
    8024493
  • 项目类别:
  • 资助金额:
    $37.5万
  • 财政年份:
    2009
  • 负责人:
    Mark Damian Wewers
  • 依托单位:
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