Gene transfer therapy in vascular diseases.

M. McKay, M. Gaballa
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引用次数: 9

Abstract

Somatic gene therapy of vascular diseases is a promising new field in modern medicine. Recent advancements in gene transfer technology have greatly evolved our understanding of the pathophysiologic role of candidate disease genes. With this knowledge, the expression of selective gene products provides the means to test the therapeutic use of gene therapy in a multitude of medical conditions. In addition, with the completion of genome sequencing programs, gene transfer can be used also to study the biologic function of novel genes in vivo. Novel genes are delivered to targeted tissue via several different vehicles. These vectors include adenoviruses, retroviruses, plasmids, plasmid/liposomes, and oligonucleotides. However, each one of these vectors has inherent limitations. Further investigations into developing delivery systems that not only allow for efficient, targeted gene transfer, but also are stable and nonimmunogenic, will optimize the clinical application of gene therapy in vascular diseases. This review further discusses the available mode of gene delivery and examines six major areas in vascular gene therapy, namely prevention of restenosis, thrombosis, hypertension, atherosclerosis, peripheral vascular disease in congestive heart failure, and ischemia. Although we highlight some of the recent advances in the use of gene therapy in treating vascular disease discovered primarily during the past two years, many excellent studies published during that period are not included in this review due to space limitations. The following is a selective review of practical uses of gene transfer therapy in vascular diseases. This review primarily covers work performed in the last 2 years. For earlier work, the reader may refer to several excellent review articles. For instance, Belalcazer et al. (6) reviewed general aspects of somatic gene therapy and the different vehicles used for the delivery of therapeutic genes. Gene therapy in restenosis and stimulation of angiogenesis in the cardiac muscle are discussed in reviews by several investigators (13,26,57,74,83). In another review, Meyerson et al. (43) discuss advances in gene therapy for vascular proliferative disorders and chronic peripheral and cardiac ischemia.
血管疾病的基因转移治疗。
血管疾病的体细胞基因治疗是现代医学中一个很有前途的新领域。基因转移技术的最新进展极大地促进了我们对候选疾病基因的病理生理作用的理解。有了这些知识,选择性基因产物的表达提供了在多种医学条件下测试基因疗法治疗用途的手段。此外,随着基因组测序程序的完成,基因转移也可用于研究新基因在体内的生物学功能。新基因通过几种不同的载体传递到目标组织。这些载体包括腺病毒、逆转录病毒、质粒、质粒/脂质体和寡核苷酸。然而,这些向量都有其固有的局限性。进一步研究开发递送系统,不仅允许高效,靶向基因转移,而且稳定和非免疫原性,将优化血管疾病基因治疗的临床应用。本文进一步讨论了基因传递的可用模式,并探讨了血管基因治疗的六个主要领域,即预防再狭窄、血栓形成、高血压、动脉粥样硬化、充血性心力衰竭外周血管疾病和缺血。虽然我们重点介绍了在过去两年中主要发现的使用基因疗法治疗血管疾病的一些最新进展,但由于篇幅限制,在此期间发表的许多优秀研究未包括在本综述中。以下是基因转移治疗在血管疾病中的实际应用的选择性回顾。该审查主要涵盖过去2年的工作。对于早期的工作,读者可以参考几篇优秀的评论文章。例如,Belalcazer等人(6)回顾了体细胞基因治疗的一般方面以及用于传递治疗基因的不同载体。基因治疗在再狭窄和刺激血管生成在心肌中被几个研究者讨论(13,26,57,74,83)。在另一篇综述中,Meyerson等人(43)讨论了血管增殖性疾病和慢性外周和心脏缺血的基因治疗进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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