以 LPS 为靶标的含布鲁氏菌三价免疫原的聚乙烯亚胺纳米结构在小鼠模型中的免疫原性。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Mansoureh Iranikhah, Razieh Nazari, Mahdi Fasihi-Ramandi, Ramezan Ali Taheri, Mohsen Zargar
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引用次数: 0

摘要

布鲁氏菌是一种细胞内革兰氏阴性球菌。它无芽孢,在巨噬细胞吞噬体中繁殖。由于纳米结构具有控制释放曲线和保护药物分子的能力,将其用作药物和疫苗载体最近受到了关注。本研究提出了一种合适的纳米聚乙烯亚胺配方,可用作免疫佐剂和 LPS 以及 TF、BP26 和 omp31 的三价候选抗原,以选择性地刺激免疫反应。通过数据库和生物信息学软件设计和评估免疫原性结构后,在大肠杆菌 BL21 中进行了重组蛋白克隆和基因表达。从培养细胞中提取该蛋白,并用 Ni-NTA 柱纯化。将抗原置于聚乙烯亚胺纳米结构中后,评估了纳米颗粒的各种特性,包括其尺寸、ZETA电位、小鼠注射和吸入保留率、扩散效力和抗原结合评估。小鼠在第 0、10、24 和 38 天分别接受不同组抗原和纳米颗粒的治疗。最后一次注射两周后,调查了脾脏细胞中细胞因子的水平,包括 IFN-γ、IL-4 和 IL-12。还评估了血清中 IgG2a 和 IgG1 抗体的浓度。与对照组相比,IgG1、IgG2a、IFN-γ21、IL-12 和 IL-4 的产生与反应一致(P<0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunogenicity of Brucella Trivalent Immunogen-Containing Polyethyleneimine Nanostructure Targeted with LPS in a Mouse Model.

Brucella is a facultative intracellular gram-negative coccobacillus. It is nonsporulating and reproduced in macrophage phagosomes. The use of nanostructures as drug and vaccine carriers has recently received attention due to their ability to control the release profile and protect the drug molecules. This study presents a suitable nano-polyethyleneimine formulation to be used as an immunoadjuvant and LPS along with trivalent candidate antigens of TF, BP26, and omp31 to selectively stimulate the immune response. After designing and evaluating the immunogenic structure by databases and bioinformatics software, recombinant protein cloning and gene expression were performed in Escherichia coli BL21 bacteria. This protein was extracted from the cultured cells, purified by Ni-NTA column. After placing the antigen inside the polyethyleneimine nanostructure, various properties of the nanoparticles, including their size, zeta potential, and retention rate for injection and inhalation of mice, diffusion efficacy, and antigen binding evaluation were evaluated. Mice were treated with different groups of antigens and nanoparticles on days 0, 10, 24, and 38. Two weeks after the last injection, the level of cytokines were investigated in spleen cells, including IFN-γ, IL-4, and IL-12. The serum concentration of IgG2a and IgG1 antibodies were also assessed. The response was consistent with significant production of IgG1, IgG2a, IFN-γ21, IL-12, and IL-4 compared to the controls (P < 0.05). Compared to the positive and negative control groups, recombinant protein and nanoparticles showed a good response in subsequent injections with live bacterial strains. The present study also revealed the potential of the developed recombinant protein as a candidate in the design and manufacture of subunit vaccines against Brucella species. This protein stimulates cellular and humoral immune responses compared to the positive control groups. These findings can be useful in the prevention and control of brucellosis and pave the way for further research by researchers around the world.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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