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动脉粥样硬化病变的抑制与消退

Inhibition and regression of atherosclerotic lesions.

作者信息

Oka Kazuhiro, Chan Lawrence

机构信息

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA.

出版信息

Acta Biochim Pol. 2005;52(2):311-9. Epub 2005 Jun 3.

Abstract

Atherosclerosis, once believed to be a result of a slow, irreversible process resulting from lipid accumulation in arterial walls, is now recognized as a dynamic process with reversibility. Liver-directed gene therapy for dyslipidemia aims to treat patients who are not responsive to currently available primary and secondary prevention. Moreover, gene therapy strategies have also proved valuable in studying the dynamics of atherosclerotic lesion formation, progression, and remodeling in experimental animals. Recent results on the long-term effect of gene therapy suggest that hepatic expression of therapeutic genes suppresses inflammation and has profound effects on the nature of the atherogenic process.

摘要

动脉粥样硬化曾被认为是动脉壁脂质积累导致的缓慢、不可逆过程的结果,现在被认为是一个具有可逆性的动态过程。针对血脂异常的肝脏定向基因治疗旨在治疗对目前可用的一级和二级预防无反应的患者。此外,基因治疗策略在研究实验动物动脉粥样硬化病变形成、进展和重塑的动态过程中也已证明具有价值。关于基因治疗长期效果的最新结果表明,治疗性基因的肝脏表达可抑制炎症,并对动脉粥样硬化过程的性质产生深远影响。

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本文引用的文献

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Apolipoprotein E and atherosclerosis: beyond lipid effect.载脂蛋白E与动脉粥样硬化:脂质效应之外
Arterioscler Thromb Vasc Biol. 2005 Feb;25(2):267-9. doi: 10.1161/01.ATV.0000154570.50696.2c.
5
Immunomodulation of atherosclerosis: implications for vaccine development.动脉粥样硬化的免疫调节:对疫苗研发的启示
Arterioscler Thromb Vasc Biol. 2005 Jan;25(1):18-28. doi: 10.1161/01.ATV.0000149142.42590.a2. Epub 2004 Oct 28.
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Current management of severe homozygous hypercholesterolaemias.重度纯合子高胆固醇血症的当前管理
Curr Opin Lipidol. 2004 Aug;15(4):413-22. doi: 10.1097/01.mol.0000137222.23784.2a.

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