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基因治疗在治疗动脉粥样硬化中的前景与进展

Prospect and progress of gene therapy in treating atherosclerosis.

作者信息

Kivelä Annukka M, Huusko Jenni, Ylä-Herttuala Seppo

机构信息

a 1 University of Eastern Finland, A.I. Virtanen Institute for Molecular Sciences, Department of Biotechnology and Molecular Medicine , Kuopio, Finland +358 403 552 075 ;

b 2 Science Service Center , Kuopio, Finland.

出版信息

Expert Opin Biol Ther. 2015;15(12):1699-712. doi: 10.1517/14712598.2015.1084282. Epub 2015 Aug 31.

Abstract

INTRODUCTION

Despite considerable improvements in therapies, atherosclerotic cardiovascular diseases remain the leading cause of death worldwide. Therefore, in addition to current treatment options, new therapeutic approaches are still needed.

AREAS COVERED

In this review, novel gene and RNA interference-based therapy approaches and promising target genes for treating atherosclerosis are addressed. In addition, relevant animal models for the demonstration of the efficacy of different gene therapy applications, and current progress toward more efficient, targeted and safer gene transfer vectors are reviewed.

EXPERT OPINION

Atherosclerosis represents a complex multifactorial disease that is dependent on the interplay between lipoprotein metabolism, cellular reactions and inflammation. Recent advances and novel targets, especially in the field of RNA interference-based therapies, are very promising. However, it should be noted that the modulation of a particular gene is not as clearly associated with a complex polygenic disease as it is in the case of monogenic diseases. A deeper understanding of molecular mechanisms of atherosclerosis, further progress in vector development and the demonstration of treatment efficacy in relevant animal models will be required before gene therapy of atherosclerosis meets its clinical reality.

摘要

引言

尽管治疗方法有了显著改进,但动脉粥样硬化性心血管疾病仍然是全球主要的死亡原因。因此,除了现有的治疗选择外,仍需要新的治疗方法。

涵盖领域

在本综述中,探讨了基于基因和RNA干扰的新型治疗方法以及治疗动脉粥样硬化的有前景的靶基因。此外,还综述了用于证明不同基因治疗应用疗效的相关动物模型,以及在开发更高效、靶向性更强和更安全的基因传递载体方面的当前进展。

专家观点

动脉粥样硬化是一种复杂的多因素疾病,取决于脂蛋白代谢、细胞反应和炎症之间的相互作用。近期的进展和新的靶点,特别是在基于RNA干扰的治疗领域,非常有前景。然而,应该注意的是,与单基因疾病不同,调节特定基因与这种复杂的多基因疾病的关联并不那么明确。在动脉粥样硬化的基因治疗成为临床现实之前,需要更深入地了解动脉粥样硬化的分子机制,在载体开发方面取得进一步进展,并在相关动物模型中证明治疗效果。

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