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基因向脉管系统的转移:历史视角及对未来研究目标的启示

Gene transfer to the vasculature: historical perspective and implication for future research objectives.

作者信息

George Sarah J, Baker Andrew H

机构信息

Bristol Heart Institute, Bristol Royal Infirmary, UK.

出版信息

Mol Biotechnol. 2002 Oct;22(2):153-64. doi: 10.1385/MB:22:2:153.

DOI:10.1385/MB:22:2:153
PMID:12405263
Abstract

Cardiovascular diseases are a major cause of fatality, disability, and economic burden in Western civilization. Although the pharmaceutical industry has delivered a plethora of drugs for treatment of diverse cardiovascular complaints, there remain many conditions for which pharmacological regimens are either nonexistent or largely ineffective. In contrast, remarkable progress has been made in the field of vascular gene transfer in the last decade. The vast majority of studies are preclinical, although a number of high profile vascular gene therapy clinical trials are in progress. In principle, vascular gene therapy represents an unprecedented opportunity to treat a host of cardiovascular diseases in humans although many scientific, clinical, and ethical obstacles remain. Here we discuss the rapid progress in preclinical vascular gene therapy, highlight the most appropriate gene delivery vectors, and discuss the advances toward the ultimate goal of an efficient and safe gene therapy for diverse cardiovascular diseases.

摘要

心血管疾病是西方文明中导致死亡、残疾和经济负担的主要原因。尽管制药行业已提供了大量药物用于治疗各种心血管疾病,但仍有许多病症不存在有效的药物治疗方案或药物治疗效果甚微。相比之下,在过去十年中,血管基因转移领域取得了显著进展。尽管多项备受瞩目的血管基因治疗临床试验正在进行,但绝大多数研究仍处于临床前阶段。原则上,血管基因治疗为治疗人类多种心血管疾病提供了前所未有的机会,尽管仍存在许多科学、临床和伦理障碍。在此,我们将讨论临床前血管基因治疗的快速进展,重点介绍最合适的基因传递载体,并探讨在实现针对各种心血管疾病的高效安全基因治疗这一最终目标方面所取得的进展。

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本文引用的文献

1
Gene therapy for the treatment of peripheral vascular disease and coronary artery disease.
Drugs Today (Barc). 2000 Sep;36(9):609-17. doi: 10.1358/dot.2000.36.9.593778.
2
Observed incidence of tumorigenesis in long-term rodent studies of rAAV vectors.重组腺相关病毒载体长期啮齿动物研究中观察到的肿瘤发生发生率。
Gene Ther. 2001 Sep;8(17):1343-6. doi: 10.1038/sj.gt.3301541.
3
Combined transductional and transcriptional targeting improves the specificity of transgene expression in vivo.转导靶向与转录靶向相结合可提高体内转基因表达的特异性。
Nat Biotechnol. 2001 Sep;19(9):838-42. doi: 10.1038/nbt0901-838.
4
Human heme oxygenase-1 gene transfer lowers blood pressure and promotes growth in spontaneously hypertensive rats.人血红素加氧酶-1基因转移可降低自发性高血压大鼠的血压并促进其生长。
Hypertension. 2001 Aug;38(2):210-5. doi: 10.1161/01.hyp.38.2.210.
5
Local gene transfer of tissue inhibitor of metalloproteinase-2 influences vein graft remodeling in a mouse model.金属蛋白酶组织抑制剂-2的局部基因转移影响小鼠模型中的静脉移植物重塑。
Arterioscler Thromb Vasc Biol. 2001 Aug;21(8):1275-80. doi: 10.1161/hq0801.093658.
6
Angiogenesis gene therapy to rescue ischaemic tissues: achievements and future directions.用于挽救缺血组织的血管生成基因治疗:成就与未来方向。
Br J Pharmacol. 2001 Aug;133(7):951-8. doi: 10.1038/sj.bjp.0704155.
7
Analysis of cell-specific promoters for viral gene therapy targeted at the vascular endothelium.
Hypertension. 2001 Jul;38(1):65-70. doi: 10.1161/01.hyp.38.1.65.
8
Extrachromosomal recombinant adeno-associated virus vector genomes are primarily responsible for stable liver transduction in vivo.染色体外重组腺相关病毒载体基因组主要负责体内肝脏的稳定转导。
J Virol. 2001 Aug;75(15):6969-76. doi: 10.1128/JVI.75.15.6969-6976.2001.
9
Wild-type p53 gene transfer inhibits neointima formation in human saphenous vein by modulation of smooth muscle cell migration and induction of apoptosis.野生型p53基因转移通过调节平滑肌细胞迁移和诱导凋亡来抑制人隐静脉新生内膜形成。
Gene Ther. 2001 May;8(9):668-76. doi: 10.1038/sj.gt.3301431.
10
Improved adenoviral vector for vascular gene therapy : beneficial effects on vascular function and inflammation.用于血管基因治疗的改良腺病毒载体:对血管功能和炎症的有益作用
Circ Res. 2001 May 11;88(9):911-7. doi: 10.1161/hh0901.090926.