Li Guo Ping, Liu Zhi Gang, Liao Bin, Zhong Nan Shan
Inflammation & Allergic Disease Lab, Affiliated Hospital of Luzhou Medical College, Luzhou 646000, Sichuan, China.
Cell Mol Immunol. 2009 Feb;6(1):45-50. doi: 10.1038/cmi.2009.6.
This study was to prepare the chitosan-pDer p 2 nanoparticles and to investigate the effect of chitosan-DNA nanoparticles on immune response in mice by oral delivery of chitosan-DNA nanoparticles. The nanoparticles were synthesized by complexing chitosan with plasmid DNA. The DNA was fully complexed into chitosan-DNA nanoparticles, suggesting a 100% encapsulation efficiency. Chitosan-DNA complex renders a significant protection of the plasmid. No effect on cell viability was observed in both cell types and average cell viability over 100% was obtained. Oral gene delivery with chitosan-DNA nanoparticles can generate a higher level expression of gene in vivo. Oral chitosan-pDer p 2 nanoparticles in BALB/c mice can induce IFN-gamma in serum and prevent subsequent sensitization of Th2 cell-regulated specific IgE responses. The data indicate that the oral administration of chitosan-pDer p 2 nanoparticles results in the expression of Der p 2 in the epithelial cells of both stomach and small intestine and the induction of Th1-type immune response.
本研究旨在制备壳聚糖-pDer p 2纳米颗粒,并通过口服壳聚糖-DNA纳米颗粒来研究其对小鼠免疫反应的影响。纳米颗粒通过壳聚糖与质粒DNA复合而成。DNA完全复合到壳聚糖-DNA纳米颗粒中,表明包封效率为100%。壳聚糖-DNA复合物对质粒有显著的保护作用。在两种细胞类型中均未观察到对细胞活力的影响,且平均细胞活力超过了100%。口服壳聚糖-DNA纳米颗粒进行基因递送可在体内产生更高水平的基因表达。在BALB/c小鼠中口服壳聚糖-pDer p 2纳米颗粒可诱导血清中的干扰素-γ,并预防随后Th2细胞调节的特异性IgE反应的致敏。数据表明,口服壳聚糖-pDer p 2纳米颗粒可导致胃和小肠上皮细胞中Der p 2的表达,并诱导Th1型免疫反应。