Wang Yarun, Wang Yue, Kang Ning, Liu Yongliang, Shan Wenjun, Bi Shengli, Ren Lei, Zhuang Guohong
Department of Biomaterials and Fujian Collaborative Innovation Center for Exploitation and Utilization of Marine Biological Resources, College of Materials, Xiamen University, Xiamen, 361005, People's Republic of China.
Organ Transplantation Institute, Anti-Cancer Research Center, Medical College, Xiamen University, Xiamen, 361005, People's Republic of China.
Nanoscale Res Lett. 2016 Dec;11(1):338. doi: 10.1186/s11671-016-1554-y. Epub 2016 Jul 19.
Different types of vaccines have been developed to elicit active immunization to treat various diseases, while suffer from limitation of efficacy. Herein, a novel immunostimulatory nanocomposite (CpG-Au@HBc VLP) was rationally designed by self-assembling engineered virus-like particles encapsulating CpG-gold nanoparticle conjugates through electrostatic interactions. The monodispersed and uniformly sized CpG-Au@HBc VLP showed increased CD4(+), CD8(+) T cell numbers and stronger secretion of cytokine interferon-gamma than HBc VLPs adjuvanted with conventional Freund's adjuvant. Furthermore, the use of Au nanoparticles also generated enhanced immunogenicity of CpG and VLPs on both humoral and cellular immune pathways, as followed from increased expressions of total HBc-specific antibody titer, CD4(+) T cells, CD8(+) T cells, cytokine interleukin-4, and interferon-gamma. These findings demonstrated that CpG-Au@HBc VLP nanocomposite could induce robust cellular and humoral immune response, which could be a potential vaccine for future prophylactic and therapeutic application.
已经开发出不同类型的疫苗来引发主动免疫以治疗各种疾病,但存在疗效受限的问题。在此,通过静电相互作用自组装包裹CpG-金纳米颗粒共轭物的工程化病毒样颗粒,合理设计了一种新型免疫刺激纳米复合材料(CpG-Au@HBc VLP)。与用传统弗氏佐剂佐剂的HBc VLP相比,单分散且尺寸均匀的CpG-Au@HBc VLP显示出CD4(+)、CD8(+) T细胞数量增加以及细胞因子干扰素-γ的分泌更强。此外,金纳米颗粒的使用还在体液和细胞免疫途径上增强了CpG和VLP的免疫原性,这表现为总HBc特异性抗体滴度、CD4(+) T细胞、CD8(+) T细胞、细胞因子白细胞介素-4和干扰素-γ的表达增加。这些发现表明,CpG-Au@HBc VLP纳米复合材料可以诱导强大的细胞和体液免疫反应,这可能是未来预防性和治疗性应用的潜在疫苗。