Liu Junfeng, Wang Jin, Zhu Qiqiang, Yu Chunqiang, Yin Jianrong, Zheng Longpo, Li Ang
J Biomed Nanotechnol. 2019 Jul 1;15(7):1454-1467. doi: 10.1166/jbn.2019.2790.
CpG ODN acts as a 'pathogen-associated' molecular pattern that is recognized by intracellular Toll-like receptor 9 and can induce a robust dendritic cells (DCs) activation to against various diseases. However, the CpG ODN is restricted with critical defects of easily enzymolysis and negligible phagocytosis. To overcome these issues, a simpler and competent nanocarrier of mannose modified PEGylated branched PEI (PEI-PEG-Man) was designed to achieve excellent DCsspecific delivery of CpG. Nanoparticles of PEI-PEG-Man encapsulating CpG (PEI-PEG-Man@CpG) possessed elevated gene loading capacity, biological stability and admirable anti-enzymolysis ability. PEI-PEG-Man@CpG could be selectively uptake by DCs through a receptor-mediated endocytosis, which generates a potent immunostimulatory activity on bone marrow derived dendritic cells (BMDCs) evidenced by significantly upregulation of the pro and anti-inflammatory cytokines (TNF-, IL-6) and the co-stimulatory molecules (CD40, CD80, CD86, and MHC class II) on BMDCs . More importantly, the results of targeting assay showed that PEI-PEG-Man@CpG nanoparticles could remarkably boost CpG accumulation in lymph lodes upon subcutaneous administration in C57BL/6 mice, which facilitated maturation of DCs and productions of anti-inflammatory cytokines. Our results suggested that PEI-PEG-Man@CpG nanoparticles, in the future, might function as a powerful vector for engineering to promote DC targeting and maturation, which enhance vaccine efficiency against cancer or infectious disease.
CpG寡脱氧核苷酸作为一种“病原体相关”分子模式,可被细胞内Toll样受体9识别,并能诱导强大的树突状细胞(DCs)活化以对抗各种疾病。然而,CpG寡脱氧核苷酸存在严重缺陷,即易被酶解且吞噬作用可忽略不计。为克服这些问题,设计了一种更简单且有效的甘露糖修饰聚乙二醇化支链聚乙烯亚胺纳米载体(PEI-PEG-Man),以实现对CpG的优异DC特异性递送。包裹CpG的PEI-PEG-Man纳米颗粒(PEI-PEG-Man@CpG)具有提高的基因负载能力、生物稳定性和令人钦佩的抗酶解能力。PEI-PEG-Man@CpG可通过受体介导的内吞作用被DCs选择性摄取,这对骨髓来源的树突状细胞(BMDCs)产生了强大的免疫刺激活性,表现为BMDCs上促炎和抗炎细胞因子(TNF-、IL-6)以及共刺激分子(CD40、CD80、CD86和MHC II类分子)显著上调。更重要的是,靶向分析结果表明,在C57BL/6小鼠皮下给药后,PEI-PEG-Man@CpG纳米颗粒可显著提高CpG在淋巴结中的积累,这促进了DCs的成熟和抗炎细胞因子的产生。我们的结果表明,未来PEI-PEG-Man@CpG纳米颗粒可能作为一种强大的载体用于工程设计,以促进DC靶向和成熟,从而提高针对癌症或传染病的疫苗效率。