Gholizadeh Afshin, Shapoury Reza, Pakzad Parviz, Mahdavi Mehdi, Danafar Hossein
Department of Microbiology, Faculty of Sciences, North Tehran Branch, Islamic Azad University, Tehran, I.R. Iran.
Department of Microbiology, Faculty of Sciences, Zanjan Branch, Islamic Azad University, Zanjan, I.R. Iran.
Res Pharm Sci. 2022 Jul 14;17(4):360-371. doi: 10.4103/1735-5362.350237. eCollection 2022 Aug.
is known as a pathogen with antibiotic resistance, causing respiratory infections. PLGA has been approved for use in vaccines as well as drug delivery. This study was performed to evaluate PLGA nanoparticles containing the outer membrane proteins (OMPs) of in stimulating the mice's immune system and improving pneumonia.
Double emulsion solvent evaporation technique was used. The properties of the obtained nanospheres were determined using a zetasizer, FTIR, and AFM devices. Nanoparticles were administered to mice BALB/c by applying the intramuscular route. ELISA was used to measure the amounts of immunoglobulins produced; also, an opsonophagocytic killing assay was used to measure the effectiveness of immunoglobulins. Immunized mice were then challenged with live through the lungs; their internal organs were also removed for bacteriological studies.
FINDINGS/RESULTS: The prepared particles were 550 nm in diameter with a negative surface charge. The production of the OMPs specific IgG was much higher in the group receiving nanoparticles containing antigen as compared to those getting pure antigen. The immunoglobulins produced against nanoparticles were superior to those developed against pure antigens. Mice that received the new nanovaccine were more resistant to pneumonia caused by this bacterium than those that received pure antigen.
Overall, it can be said that PLGA nanoparticles could deliver their internal antigens (OMPs) well to the immune system of mice and stimulate humoral immunity in these animals, thus protecting them against pneumonia caused by .
已知为具有抗生素抗性的病原体,可引起呼吸道感染。聚乳酸-羟基乙酸共聚物(PLGA)已被批准用于疫苗以及药物递送。本研究旨在评估含有外膜蛋白(OMPs)的PLGA纳米颗粒对小鼠免疫系统的刺激作用以及改善肺炎的效果。
采用双乳液溶剂蒸发技术。使用zeta电位仪、傅里叶变换红外光谱仪(FTIR)和原子力显微镜(AFM)设备测定所得纳米球的性质。通过肌肉注射途径将纳米颗粒给予BALB/c小鼠。采用酶联免疫吸附测定(ELISA)法测量产生的免疫球蛋白量;此外,采用调理吞噬杀伤试验测量免疫球蛋白的有效性。然后通过肺部对免疫小鼠进行活菌攻击;还取出它们的内脏进行细菌学研究。
制备的颗粒直径为550nm,表面带负电荷。与接受纯抗原的组相比,接受含抗原纳米颗粒的组中OMPs特异性IgG的产生要高得多。针对纳米颗粒产生的免疫球蛋白优于针对纯抗原产生的免疫球蛋白。接受新型纳米疫苗的小鼠比接受纯抗原的小鼠对这种细菌引起的肺炎更具抵抗力。
总体而言,可以说PLGA纳米颗粒能够将其内部抗原(OMPs)很好地递送至小鼠免疫系统并刺激这些动物的体液免疫,从而保护它们免受引起的肺炎。