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Bioactive baculovirus nanohybrids for stent based rapid vascular re-endothelialization

机译:生物活性杆状病毒纳米杂交技术用于基于支架的快速血管再内皮化

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摘要

Present study, for the first time, reports the development of a nanohybridized baculovirus based stent that can locally promote vascular re-endothelialization by efficient delivery of pro-angiogenic vascular endothelial growth factor (Vegf) genes. In vitro data demonstrated rapid expression of functionally active Vegf by the bioactive stent-transduced vascular cells. In vivo site-specific transgene expression was observed at the stented regions of balloon-denuded canine femoral artery, which eventually lead to significant endothelial recovery at the injured sites. A significant reduction in neointima formation (2.23 ± 0.56 mm2 vs 2.78 ± 0.49 mm2 and 3.11 ± 0.23 mm2, p < 0.05; n = 8) and percent stenosis was observed in treated stent group compared to negative control and bare metal stent groups. These findings collectively implicate the potential of this newly developed baculovirus based biotherapeutic stent to ameliorate damaged vascular biology and attenuate re-narrowing of stented artery by inhibiting neointima formation.
机译:本研究首次报道了基于纳米杂交杆状病毒的支架的开发,该支架可通过有效递送促血管生成的血管内皮生长因子(Vegf)基因来局部促进血管再内皮化。体外数据表明,具有生物活性的支架转导的血管细胞可快速表达具有功能活性的Vegf。在球囊裸露的犬股动脉的支架区域观察到体内位点特异性转基因表达,这最终导致受伤部位的内皮显着恢复。新内膜形成显着减少(2.23±0.56 mm 2 与2.78±0.49 mm 2 和3.11±0.23 mm 2 ,p <0.05; n = 8),与阴性对照组和裸金属支架组相比,治疗后支架组的狭窄百分比更高。这些发现共同暗示了这种新开发的基于杆状病毒的生物治疗支架潜在的潜力,可以通过抑制新内膜的形成来改善受损的血管生物学,并减轻支架动脉的再狭窄。

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