Department of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Nanoscale Science Program, Department of Chemistry, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Adv Drug Deliv Rev. 2021 Jun;173:427-438. doi: 10.1016/j.addr.2021.04.011. Epub 2021 Apr 20.
Nucleic acid nanoparticles (NANPs) represent a highly versatile molecular platform for the targeted delivery of various therapeutics. However, despite their promise, further clinical translation of this innovative technology can be hindered by immunological off-target effects. All human cells are equipped with an arsenal of receptors that recognize molecular patterns specific to foreign nucleic acids and understanding the rules that guide this recognition offer the key rationale for the development of therapeutic NANPs with tunable immune stimulation. Numerous recent studies have provided increasing evidence that in addition to NANPs' physicochemical properties and therapeutic effects, their interactions with cells of the immune system can be regulated through multiple independently programmable architectural parameters. The results further suggest that defined immunomodulation by NANPs can either support their immunoquiescent delivery or be used for conditional stimulation of beneficial immunological responses.
核酸纳米颗粒(NANPs)是一种非常灵活的分子平台,可用于靶向递各种治疗药物。然而,尽管这项创新技术具有广阔的应用前景,但它在临床上的进一步转化可能会受到免疫非靶向效应的阻碍。所有的人体细胞都配备了一套受体,这些受体能够识别特定于外来核酸的分子模式,而理解指导这种识别的规则则为开发具有可调免疫刺激作用的治疗性 NANPs 提供了关键依据。最近的许多研究都提供了越来越多的证据表明,除了 NANPs 的物理化学性质和治疗效果外,它们与免疫系统细胞的相互作用可以通过多个独立的可编程结构参数来调节。这些结果还表明,NANPs 可以通过定义性的免疫调节,要么支持其免疫惰性递,要么用于条件性地刺激有益的免疫反应。