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Assessment of Genetic Shielding for Adenovirus Vectors

机译:腺病毒载体的遗传屏蔽评估

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Development of adenovirus (Ad) vectors in the clinical context has highlighted that vector efficacy may be limited by the host humoral response due to pre-existing titers of neutralizing antibodies against the vector itself in humans. Further, multiple dosing of Ad vectors based on serotype 5 would be limited. Current immune evasion strategies being investigated by other laboratories are only applicable to non-replicating vectors. Therefore we have proposed genetic shielding as an alternate that would be applicable to both non-replicating and conditionally replicating Ad vectors. Genetic shielding would encapsulate fusion of a self-protein to Ad minor capsid protein, pIX, as a means to cloak immunogenic capsid epitopes and prevent neutralization of Ad vectors through Ad specific antibodies. In the development of a suitably shielded Ad vector we choose several self-proteins that we attempted to fuse to pIX. We have also used an indirect method to conjugate albumin to the capsid through an albumin binding domain fused to pIX. Despite attaining novel pIX modified Ad vectors we found that none of the pIX attached molecules in this study prevented neutralizing antibodies from halting gene transfer.
机译:在临床背景下,腺病毒(Ad)载体的开发突显出,由于人体中预先存在针对抗体本身的中和抗体滴度,因此载体功效可能受到宿主体液反应的限制。此外,基于血清型5的Ad载体的多次给药将受到限制。其他实验室正在研究的当前免疫逃避策略仅适用于非复制型载体。因此,我们提出了遗传屏蔽作为替代方案,其可适用于非复制和有条件复制的Ad载体。遗传屏蔽将封装自身蛋白与Ad小衣壳蛋白pIX的融合,以此掩盖免疫原性衣壳表位并防止通过Ad特异性抗体中和Ad载体。在开发适当屏蔽的Ad载体时,我们选择了几种试图融合到pIX的自身蛋白。我们还使用了一种间接方法,通过与pIX融合的白蛋白结合域将白蛋白缀合到衣壳上。尽管获得了新颖的pIX修饰的Ad载体,我们发现在这项研究中没有一个pIX附着分子阻止中和抗体阻止基因转移。

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