Department of Chemistry, University of Massachusetts Amherst, 710 North Pleasant Street, Amherst, MA 01003, USA.
Department of Chemistry, University of Massachusetts Amherst, 710 North Pleasant Street, Amherst, MA 01003, USA; ShenYang Pharmaceutical University, No. 103 Wenhua Road, Shenyang 110016, China.
J Control Release. 2018 Aug 10;283:235-240. doi: 10.1016/j.jconrel.2018.06.001. Epub 2018 Jun 5.
The use of nanoparticle-stabilized nanocapsules for cytosolic siRNA delivery for immunomodulation in vitro and in vivo is reported. These NPSCs deliver siRNA directly to the cytosol of macrophages in vitro with concomitant knockdown of gene expression. In vivo studies showed directed delivery of NPSCs to the spleen, enabling gene silencing of macrophages, with preliminary studies showing 70% gene knockdown at a siRNA dose of 0.28 mg/kg. Significantly, the delivery of siRNA targeting tumor necrosis factor-α efficiently silenced TNF-α expression in LPS-challenged mice, demonstrating efficacy in modulating immune response in an organ-selective manner. This research highlights the potential of the NPSC platform for targeted immunotherapy and further manipulation of the immune system.
本文报道了纳米颗粒稳定的纳米胶囊在细胞浆内递送 siRNA 以进行免疫调节的应用。这些 NPSC 可将 siRNA 直接递送至体外巨噬细胞的细胞浆中,同时实现基因表达的下调。体内研究表明,NPSC 可定向递送至脾脏,使巨噬细胞中的基因沉默,初步研究表明,在 siRNA 剂量为 0.28mg/kg 时,基因敲低率达到 70%。重要的是,针对肿瘤坏死因子-α(TNF-α)的 siRNA 的递呈可有效沉默 LPS 刺激的小鼠中 TNF-α 的表达,表明其具有以器官选择性方式调节免疫反应的功效。该研究强调了 NPSC 平台在靶向免疫治疗和进一步操纵免疫系统方面的潜力。