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粒径对颗粒排驱动力学和抗体反应的影响。

The impact of size on particle drainage dynamics and antibody response.

机构信息

Department of BioMedical Research, University of Bern, Bern, Switzerland; Department of Immunology RIA, University Hospital Bern, Bern, Switzerland.

Latvian Biomedical Research & Study Centre, Ratsupites iela 1, Riga, LV 1067, Latvia.

出版信息

J Control Release. 2021 Mar 10;331:296-308. doi: 10.1016/j.jconrel.2021.01.012. Epub 2021 Jan 12.

Abstract

Vaccine-induced immune response can be greatly enhanced by mimicking pathogen properties. The size and the repetitive geometric shape of virus-like particles (VLPs) influence their immunogenicity by facilitating drainage to secondary lymphoid organs and enhancing interaction with and activation of B cells and innate humoral immune components. VLPs derived from the plant Bromovirus genus, specifically cowpea chlorotic mottle virus (CCMV), are T = 3 icosahedral particles. (T) is the triangulation number that refers to the number and arrangements of the subunits (pentamers and hexamers) of the VLPs. CCMV-VLPs can be easily expressed in an E. coli host system and package ssRNA during the expression process. Recently, we have engineered CCMV-VLPs by incorporating the universal tetanus toxin (TT) epitope at the N-terminus. The modified CCMV-VLPs successfully form icosahedral particles T = 3, with a diameter of ~30 nm analogous to the parental VLPs. Interestingly, incorporating TT epitope at the C-terminus of CCMV-VLPs results in the formation of Rod-shaped VLPs, ~1 μm in length and ~ 30 nm in width. In this study, we have investigated the draining kinetics and immunogenicity of both engineered forms (termed as Round-shaped CCMV-VLPs and Rod-shaped CCMV-VLPs) as potential B cell immunogens using different in vitro and in vivo assays. Our results reveal that Round-shaped CCMV-VLPs are more efficient in draining to secondary lymphoid organs to charge professional antigen-presenting cells as well as B cells. Furthermore, compared to Rod-shaped CCMV-VLPs, Round-shaped CCMV-VLPs led to more than 100-fold increased systemic IgG and IgA responses accompanied by prominent formation of splenic germinal centers. Round-shaped CCMV-VLPs could also polarize the induced T cell response toward Th1. To our knowledge, this is the first study investigating and comparing the draining kinetics and immunogenicity of one and the same VLP monomer forming nano-sized icosahedra or rods in the micrometer size.

摘要

病毒样颗粒(VLPs)通过模拟病原体的性质,可以极大地增强疫苗诱导的免疫反应。VLPs 的大小和重复的几何形状通过促进引流到次级淋巴器官并增强与 B 细胞和先天体液免疫成分的相互作用和激活,来影响其免疫原性。源自植物 Bromovirus 属的 VLPs,特别是豇豆花叶病毒(CCMV),是 T=3 二十面体颗粒。(T)是指 VLPs 亚单位(五聚体和六聚体)的数量和排列的三角数。CCMV-VLPs 可以很容易地在大肠杆菌宿主系统中表达,并在表达过程中包装 ssRNA。最近,我们通过在 N 端掺入通用破伤风毒素(TT)表位来工程化 CCMV-VLPs。修饰后的 CCMV-VLPs 成功形成 T=3 的二十面体颗粒,直径约 30nm,类似于亲本 VLPs。有趣的是,在 CCMV-VLPs 的 C 端掺入 TT 表位会导致杆状 VLPs 的形成,长度约 1μm,宽度约 30nm。在这项研究中,我们使用不同的体外和体内测定法,研究了这两种工程形式(称为圆形 CCMV-VLPs 和杆状 CCMV-VLPs)作为潜在 B 细胞免疫原的引流动力学和免疫原性。我们的结果表明,圆形 CCMV-VLPs 更有效地引流到次级淋巴器官,以给专业抗原呈递细胞和 B 细胞充电。此外,与杆状 CCMV-VLPs 相比,圆形 CCMV-VLPs 导致系统 IgG 和 IgA 反应增加 100 多倍,并伴有脾脏生发中心的明显形成。圆形 CCMV-VLPs 还可以使诱导的 T 细胞反应向 Th1 极化。据我们所知,这是第一项研究,研究和比较了同一种 VLP 单体形成纳米级二十面体或微米级杆状的引流动力学和免疫原性。

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