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.
人们希望,改构后的腺病毒在基因治疗方面能起到重要的作用,例如,作为载体基因携带治疗性基因到达细胞内。
The hope is that modified adenovirus could play a role in gene therapy, used as a vector (carrier) for delivering therapeutic genes to the interior of cells.
腺病毒载体是继逆转录病毒载体后在基因治疗、基因免疫等方面应用开发得较早且较成熟的一种基因载体。
Adenovirus vector is an earlier and maturer genetic carrier in the respect of gene therapy and genetic immunization after retroviral vector.
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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