Increased vascularity detected by digital subtraction angiography after VEGF gene transfer to human lower limb artery:: A randomized, placebo-controlled, double-blinded phase II study

被引:263
作者
Mäkinen, K
Manninen, H
Hedman, M
Matsi, P
Mussalo, H
Alhava, E
Ylä-Herttuala, S
机构
[1] Univ Kuopio, Dept Med, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, Dept Surg, FIN-70211 Kuopio, Finland
[3] Univ Kuopio, Dept Clin Radiol, FIN-70211 Kuopio, Finland
[4] Univ Kuopio, Dept Clin Physiol, FIN-70211 Kuopio, Finland
[5] Univ Kuopio, AI Virtanen Inst, FIN-70211 Kuopio, Finland
[6] Kuopio Univ Hosp, Gene Therapy Unit, SF-70210 Kuopio, Finland
关键词
angiogenesis; gene therapy; growth substances; peripheral vascular disease; angioplasty;
D O I
10.1006/mthe.2002.0638
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Vascular endothelial growth factor (VEGF) gene therapy may be useful for the treatment of lower-limb ischemia. The objectives of this study were to evaluate safety and angiographic and hemodynamic responses of local catheter-mediated VEGF gene therapy in ischemic lower-limb arteries after percutaneous transluminal angioplasty (PTA). For this study, we recruited patients with chronic lower-limb ischemia and atherosclerotic infrainguinal occlusion or stenosis suitable for PTA. In the study, 18 patients received 2 X 10(10)plaque-forming units (pfu) VEGF-adenovirus (VEGF-Ad), 17 patients received VEGF-plasmid/liposome (VEGF-P/L; 2000 mug of VEGF plasmid, 2000 mul of DOTMA:DOPE), and 19 control patients received Ringer's lactate at the angioplasty site. Digital subtraction angiography (DSA) was used to evaluate vascularity before, immediately after, and 3 months after the PTA. Clinical follow-up data, basic laboratory tests, and ankle-brachial index (ABI) were evaluated. Primary endpoint was DSA analysis of vascularity, and secondary endpoints were restenosis rate, Rutherford class, and ABI after 3 months follow-up. No major gene transfer-related side effects or differences in laboratory tests were detected between the study groups. However, anti-adenovirus antibodies increased in 61% of the patients treated with VEGF-Ad. For the primary endpoint, follow-up DSA revealed increased vascularity in the VEGF-treated groups distally to the gene transfer site (VEGF-Ad P = 0.03, VEGFP/L P = 0.02) and in the VEGF-Ad group in the region of the clinically most severe ischemia (P = 0.01). As for the secondary endpoints, mean Rutherford class and ABI showed statistically significant improvements in the VEGF-Ad and VEGF-P/L groups, but similar improvements were also seen in the control patients. We conclude that catheter-mediated VEGF gene therapy is safe and well tolerated. Angiography demonstrated that VEGF gene transfer increased vascularity after PTA in both VEGF-Ad- and VEGF-P/L-treated groups.
引用
收藏
页码:127 / 133
页数:7
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