Center for Inflammation, Immunity & infection, Georgia State University Institute for Biomedical Sciences, Atlanta, GA, USA.
Center for Inflammation, Immunity & infection, Georgia State University Institute for Biomedical Sciences, Atlanta, GA, USA.
Nanomedicine. 2018 Jun;14(4):1349-1360. doi: 10.1016/j.nano.2018.03.007. Epub 2018 Apr 9.
The immunogenicity of subunit vaccines can be augmented by formulating them into nanoparticles. We conjugated recombinant trimetric influenza A/Aichi/2/68(H3N2) hemagglutinin (HA) onto functionalized gold nanoparticle (AuNP) surfaces in a repetitive, oriented configuration. To further improve the immunogenicity, we generated Toll-like receptor 5 (TLR5) agonist flagellin (FliC)-coupled AuNPs as particulate adjuvants. Intranasal immunizations with an AuNP-HA and AuNP-FliC particle mixture elicited strong mucosal and systemic immune responses that protected hosts against lethal influenza challenges. Compared with the AuNP-HA alone group, the addition of AuNP-FliC improved mucosal B cell responses as characterized by elevated influenza specific IgA and IgG levels in nasal, tracheal, and lung washes. AuNP-HA/AuNP-FliC also stimulated antigen-specific interferon-γ (IFN-γ)-secreting CD4 cell proliferation and induced strong effector CD8 T cell activation. Our results indicate that intranasal co-delivery of antigen and adjuvant-displaying AuNPs enhanced vaccine efficacy by inducing potent cellular immune responses.
将亚单位疫苗制成纳米颗粒可以增强其免疫原性。我们将重组三价流感 A/Aichi/2/68(H3N2)血凝素(HA)以重复的、定向的方式缀合到功能化的金纳米颗粒(AuNP)表面上。为了进一步提高免疫原性,我们生成了 Toll 样受体 5(TLR5)激动剂鞭毛蛋白(FliC)偶联的 AuNP 作为颗粒佐剂。鼻内免疫接种 AuNP-HA 和 AuNP-FliC 颗粒混合物可引发强烈的黏膜和全身免疫反应,保护宿主免受致死性流感的挑战。与单独使用 AuNP-HA 相比,添加 AuNP-FliC 可改善黏膜 B 细胞反应,表现为鼻、气管和肺冲洗液中流感特异性 IgA 和 IgG 水平升高。AuNP-HA/AuNP-FliC 还刺激抗原特异性干扰素-γ(IFN-γ)分泌 CD4 细胞增殖,并诱导强烈的效应 CD8 T 细胞激活。我们的结果表明,通过诱导有效的细胞免疫反应,抗原和佐剂展示 AuNP 的鼻内共递药增强了疫苗的功效。