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探索聚合物在腺病毒介导的基因传递中的作用:逃避免疫反应和重新定向嗜性。

Exploring the functions of polymers in adenovirus-mediated gene delivery: Evading immune response and redirecting tropism.

机构信息

Department of Pharmacy, Hebei University of Science and Technology, Shijiazhuang 050018, China; State Key Laboratory Breeding Base - Hebei Province Key Laboratory of Molecular Chemistry for Drugs, Hebei University of Science and Technology, Shijiazhuang 050018, China; Hebei Research Center of Pharmaceutical and Chemical Engineering, Hebei University of Science and Technology, Shijiazhuang 050018, China.

Department of Pharmacy, Hebei University of Science and Technology, Shijiazhuang 050018, China.

出版信息

Acta Biomater. 2019 Oct 1;97:93-104. doi: 10.1016/j.actbio.2019.06.059. Epub 2019 Aug 3.

Abstract

Adenovirus (Ad) is a promising viral carrier in gene therapy because of its unique attribution. However, clinical applications of Ad vectors are currently restricted by their immunogenicity and broad native tropism. To address these obstacles, a variety of nonimmunogenic polymers are utilized to modify Ad vectors chemically or physically. In this review, we systemically discuss the functions of polymers in Ad-mediated gene delivery from two aspects: evading the host immune responses to Ads and redirecting Ad tropism. With polyethylene glycol (PEG) first in order, a variety of polymers have been developed to shield the surface of Ad vectors and well accomplished to evade the host immune response, block CAR-dependant cellular uptake, and reduce accumulation in the liver. In addition, shielding Ad vectors with targeted polymers (including targeting ligand-conjugated polymers and bio-responsive polymers) can also efficiently retarget Ad vectors to tumor tissues and reduce their distribution in nontargeted tissues. With its potential to evade the immune response and retarget Ad vectors, modification with polymers has been generally regarded as a promising strategy to facilitate the clinical applications of Ad vectors for virotherapy. STATEMENT OF SIGNIFICANCE: There is no doubt that Adenovirus (Ads) are attractive vectors for gene therapy, with high sophistication and effectiveness in overcoming both extra- and intracellular barriers, which cannot be exceeded by any other nonviral gene vectors. Unfortunately, their clinical applications are still restricted by some critical hurdles, including immunogenicity and native broad tropism. Therefore, a variety of elegant strategies have been developed from various angles to address these hurdles. Among these various strategies, coating Ads with nonimmunogenic polymers has attracted much attention. In this review, we systemically discuss the functions of polymers in Ad-mediated gene delivery from two aspects: evading the host immune responses to Ads and redirecting Ad tropism. In addition, the key factors in Ad modification with polymers have been highlighted and summarized to provide guiding theory for the design of more effective and safer polymer-Ad hybrid gene vectors.

摘要

腺病毒(Ad)因其独特的属性,成为基因治疗中很有前途的病毒载体。然而,Ad 载体的临床应用目前受到其免疫原性和广泛的天然嗜性的限制。为了解决这些障碍,各种非免疫原性聚合物被用于化学或物理修饰 Ad 载体。在这篇综述中,我们从两个方面系统地讨论了聚合物在 Ad 介导的基因传递中的作用:逃避宿主对 Ads 的免疫反应和重新定向 Ad 的嗜性。以聚乙二醇(PEG)为例,已经开发了多种聚合物来屏蔽 Ad 载体的表面,并且已经很好地完成了逃避宿主免疫反应、阻断 CAR 依赖性细胞摄取和减少在肝脏中的积累。此外,用靶向聚合物(包括靶向配体偶联聚合物和生物响应性聚合物)屏蔽 Ad 载体也可以有效地将 Ad 载体重新靶向肿瘤组织,并减少其在非靶向组织中的分布。通过聚合物的修饰来逃避免疫反应和重新靶向 Ad 载体,已经被普遍认为是促进 Ad 载体在病毒治疗中的临床应用的一种很有前途的策略。

意义陈述:毫无疑问,腺病毒(Ads)是基因治疗中很有吸引力的载体,具有高度的复杂性和有效性,可以克服细胞内外的障碍,这是任何其他非病毒基因载体都无法超越的。不幸的是,它们的临床应用仍然受到一些关键障碍的限制,包括免疫原性和天然的广泛嗜性。因此,已经从各个角度开发了各种巧妙的策略来解决这些障碍。在这些各种策略中,用非免疫原性聚合物包裹 Ads 引起了广泛关注。在这篇综述中,我们从两个方面系统地讨论了聚合物在 Ad 介导的基因传递中的作用:逃避宿主对 Ads 的免疫反应和重新定向 Ad 的嗜性。此外,还强调和总结了用聚合物修饰 Ad 的关键因素,为设计更有效和更安全的聚合物-Ad 杂交基因载体提供了指导理论。

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