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ALVEOLAR MACROPHAGES AND DEFENSE OF THE LUNG IN AIDS

ALVEOLAR MACROPHAGES AND DEFENSE OF THE LUNG IN AIDS
肺泡巨噬细胞和艾滋病中肺部的防御
批准号:
2221079
负责人:
OFRA K WEINBERGER
金额:
$18.5万
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-07-01 至 1995-06-30

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中文摘要
翻译
巨噬细胞不仅在艾滋病的发病过程中起着核心作用
英文摘要
The macrophage plays s central role in AIDS pathogenesis not only by being susceptible to HIV infection but also by serving as a major reservoir for the dissemination of virus in infected individuals. The alveolar macrophage is one of the principle cell types involved in the immune defense mechanisms of the lung. Based on our understanding of the macrophage as a critical cell in the induction of cellular immune responses, it is of great importance to study the nature of the interaction of the virus with human alveolar macrophages. The goal of this research proposal is the establishment of a system, utilizing primary human alveolar macrophages, for the analyses of macrophage function and gene expression following the introduction of HIV genes. This will involve the optimization of conditions for transfection of these cells and the transfection into alveolar macrophages of sub-genomic viral fragments as well as isolated HIV genes. Subsequently, the effect of specific viral gene expression on the expression of macrophage products and cell surface markers will be analyzed; specifically, the expression of major histocompatibility complex (MHC) class II antigens, tumor necrosis factor (TNF), interleukin- 1 (IL-1), the adherence molecules of LFA-1, Mac-1, and p150/95, FcRI and FcRII, and lysozyme. The mechanism of the modulation will be analyzed, the target of the effect will be defined, and the region(s) of functional importance in the viral gene will be determined. The activities of lymphocytotrophic and monocytotropic viruses will be compared in regard to their ability to perturb alveolar macrophage physiology. These studies will provide insight into mechaniss underlying the profound immunodeficiency which is central in AIDS pathogenesis.
期刊论文(4)
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会议论文
TAT-mediated transcellular activation of HIV-1 long terminal repeat directed gene expression by HIV-1-infected peripheral blood mononuclear cells.
TAT 介导的 HIV-1 长末端重复序列跨细胞激活 HIV-1 感染的外周血单核细胞定向基因表达。
DOI: --
发表时间: 1994
期刊: Journal of immunology (Baltimore, Md. : 1950)
影响因子: --
作者: [Thomas,CA, Dobkin,J, Weinberger,OK]
通讯作者: Weinberger,OK
Human immunodeficiency virus-1 env impairs Fc receptor-mediated phagocytosis via a cyclic adenosine monophosphate-dependent mechanism.
人类免疫缺陷病毒-1 env 通过环磷酸腺苷依赖性机制损害 Fc 受体介导的吞噬作用。
DOI: --
发表时间: 1997
期刊: Blood
影响因子: 20.3
作者: [Thomas,CA, Weinberger,OK, Ziegler,BL, Greenberg,S, Schieren,I, Silverstein,SC, ElKhoury,J]
通讯作者: ElKhoury,J
Transcellular activation of the human immunodeficiency virus type 1 long terminal repeat in T lymphocytes requires CD4-gp120 binding.
T 淋巴细胞中人类免疫缺陷病毒 1 型长末端重复序列的跨细胞激活需要 CD4-gp120 结合。
DOI: 10.1128/jvi.66.7.4536-4539.1992
发表时间: 1992
期刊: Journal of virology
影响因子: 5.4
作者: [Marcuzzi,A, Lowy,I, Weinberger,OK]
通讯作者: Weinberger,OK
Transcellular activation of the human immunodeficiency virus type 1 long terminal repeat in cocultured lymphocytes.
共培养淋巴细胞中人类免疫缺陷病毒 1 型长末端重复序列的跨细胞激活。
DOI: 10.1128/jvi.66.7.4228-4232.1992
发表时间: 1992
期刊: Journal of virology
影响因子: 5.4
作者: [Marcuzzi,A, Weinberger,J, Weinberger,OK]
通讯作者: Weinberger,OK
ALVEOLAR MACROPHAGES AND DEFENSE OF THE LUNG IN AIDS
ALVEOLAR MACROPHAGES AND DEFENSE OF THE LUNG IN AIDS
ALVEOLAR MACROPHAGES AND DEFENSE OF THE LUNG IN AIDS
ALVEOLAR MACROPHAGES AND DEFENSE OF THE LUNG IN AIDS
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