目的研究携带血管抑素K1-5 基因的腺病毒载体对其对血管内皮细胞增殖的抑制作用。

Objective To investigate the suppression effects of a adenovirus vector containing angiostatin K1-5 gene to the proliferation and migration of vascular endothelial cells.

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结论利用位置特性重组技术，成功的构建了人反义B7 - H1的腺病毒载体，为后续对B7 - H1的相关研究创造了条件。

Conclusion the recombinant adenovirus vector was constructed successfully by site-specific recombination technique, which provides a foundation for further research about B7-H1.

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Chiu补充说，伶猴腺病毒(TMAdV)在人类身上罕见，这让它可能成为一个潜在的强大工具，在基因治疗中充当病毒载体。

TMAdV's rarity in humans could make it a potentially powerful tool as a viral vehicle for delivering gene therapy, Chiu adds.

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Because of this people have sought other kinds of viruses to use as vectors and one that's commonly used is an adenovirus.

正因为如此,人们找到了其它病毒来,作为载体,常见的有,腺病毒

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But if you're trying to use that virus as a gene delivery vector and your body gets rid of it then the therapy has failed, it's ended.

但如果你想把腺病毒作为基因治疗载体,而你的身体清除这种病毒,治疗就失败了,前功尽弃了

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