Atherosclerosis: Molecular action and suppression of NKT cell subsets
动脉粥样硬化:NKT 细胞亚群的分子作用和抑制
基本信息
- 批准号:nhmrc : 436854
- 负责人:
- 金额:$ 30.59万
- 依托单位:
- 依托单位国家:澳大利亚
- 项目类别:NHMRC Project Grants
- 财政年份:2007
- 资助国家:澳大利亚
- 起止时间:2007-01-01 至 2009-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Atherosclerosis, or hardening of large arteries, is the underlying cause of up to 50% of deaths in Western communities from heart attacks and strokes. Today it is considered a chronic inflammatory disease arising from the influx of fats such as cholesterol into the inner liming of arteries that provide blood supply to organs such as the heart and the brain. However, the exact role that inflammation plays in the development of this blood vessel disease is poorly understood. This study is directed towards understanding the role of a subset of while blood cells known as NKT cells in the inflammatory process. In particular we will examine whether the activity of NKT cells in promoting atherosclerosis can be controlled either by the administration of drugs that deprive them of molecules that stimulate their activity and-or by the injection of another population of white blood cells known as regulatory T cells that may to limit their activity. Our preclinical study of atherosclerosis in mice has potential for extension to the control of atherosclerosis in humans. Successful translation in this way can be expected to provide a significant health benefit.
动脉粥样硬化或大动脉硬化是西方社区高达50%的心脏病发作和中风死亡的根本原因。今天,它被认为是一种慢性炎症性疾病,由脂肪如胆固醇流入动脉内膜引起,动脉为心脏和大脑等器官提供血液供应。然而,炎症在这种血管疾病发展中的确切作用尚不清楚。这项研究旨在了解称为NKT细胞的白细胞亚群在炎症过程中的作用。特别是,我们将研究NKT细胞促进动脉粥样硬化的活性是否可以通过给予药物来控制,使其失去刺激其活性的分子,或者通过注射另一群被称为调节性T细胞的白色血细胞来限制其活性。我们在小鼠动脉粥样硬化的临床前研究有可能扩展到人类动脉粥样硬化的控制。以这种方式成功的翻译可以预期提供显着的健康益处。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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A/Pr Peter Tipping其他文献
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{{ truncateString('A/Pr Peter Tipping', 18)}}的其他基金
Cardiac Fibrosis in Hypertensive Heart Disease: Cellular and Molecular Mechanism
高血压心脏病中的心脏纤维化:细胞和分子机制
- 批准号:
nhmrc : GNT1106151 - 财政年份:2016
- 资助金额:
$ 30.59万 - 项目类别:
Project Grants
Cardiac Fibrosis in Hypertensive Heart Disease: Cellular and Molecular Mechanism
高血压心脏病中的心脏纤维化:细胞和分子机制
- 批准号:
nhmrc : 1106151 - 财政年份:2016
- 资助金额:
$ 30.59万 - 项目类别:
Project Grants
Natural Killer (NK) Cells and Development of Atherosclerosis: Cellular and Molecular Mechanisms
自然杀伤 (NK) 细胞与动脉粥样硬化的发展:细胞和分子机制
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nhmrc : 1068500 - 财政年份:2014
- 资助金额:
$ 30.59万 - 项目类别:
Project Grants
Regulatory T cells and Cardiac Fibrosis in Hypertensive Heart Disease: Cellular and Molecular Mechanisms of Suppression
高血压性心脏病中的调节性 T 细胞和心脏纤维化:抑制的细胞和分子机制
- 批准号:
nhmrc : 1049356 - 财政年份:2013
- 资助金额:
$ 30.59万 - 项目类别:
Project Grants
BAFF and its receptors:contribution and therapeutic potential in atherosclerosis
BAFF及其受体:在动脉粥样硬化中的贡献和治疗潜力
- 批准号:
nhmrc : 1025211 - 财政年份:2012
- 资助金额:
$ 30.59万 - 项目类别:
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Proatherogenic CD4 NKT cells and atherosclerosis: molecular mechanisms and therapeutic strategies for suppression
促动脉粥样硬化 CD4 NKT 细胞和动脉粥样硬化:分子机制和抑制治疗策略
- 批准号:
nhmrc : 1030515 - 财政年份:2012
- 资助金额:
$ 30.59万 - 项目类别:
Project Grants
Role of B lymphocytes in atherosclerosis
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The role of the cytoplasmic domain of tissue factor in maintenance of the glomerular filtration barrier.
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nhmrc : 545878 - 财政年份:2009
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$ 30.59万 - 项目类别:
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Gene Regulation, Cytokine regulation
基因调控、细胞因子调控
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nhmrc : 436603 - 财政年份:2007
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$ 30.59万 - 项目类别:
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Pathogenic mechanisms of inflammatory diseases
炎症性疾病的发病机制
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$ 30.59万 - 项目类别:
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