共 48 条
VEGF gene delivery for treatment of ischemic cardiovascular disease
被引:59
作者:

Koransky, ML
论文数: 0 引用数: 0
h-index: 0
机构: Stanford Univ, Sch Med, Med Ctr, Dept Microbiol & Immunol, Stanford, CA 94305 USA

Robbins, RC
论文数: 0 引用数: 0
h-index: 0
机构: Stanford Univ, Sch Med, Med Ctr, Dept Microbiol & Immunol, Stanford, CA 94305 USA

Blau, HM
论文数: 0 引用数: 0
h-index: 0
机构: Stanford Univ, Sch Med, Med Ctr, Dept Microbiol & Immunol, Stanford, CA 94305 USA
机构:
[1] Stanford Univ, Sch Med, Med Ctr, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Cardiothorac Surg, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Mol Pharmacol, Stanford, CA 94305 USA
关键词:
D O I:
10.1016/S1050-1738(01)00158-X
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
There are increasing numbers of patients with ischemic myocardial disease not amenable to traditional methods of revascularization. These patients may benefit from new research into the use of naturally occurring angiogenic compounds, such as vascular endothelial growth factor (VEGF) for re-establishing blood flow into regions of hibernating myocardium. Animal studies and human clinical trials evaluating VEGF demonstrate increases in myocardial perfusion after treatment, with some patients reporting improvement in anginal symptoms. Further research into the ideal form of VEGF therapy (protein, plasmid, or adenoviral) and delivery method (intracoronary, intramyocardial, or epicardial) seems justified. (C) 2002, Elsevier Science Inc.
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页码:108 / 114
页数:7
相关论文
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