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Formulation High Throughput In Vitro Screening and In Vivo Functional Characterization of Nanoemulsion-Based Intranasal Vaccine Adjuvants

机译:纳米乳液为基础的鼻内疫苗佐剂的配方高通量体外筛选和体内功能表征

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摘要

Vaccine adjuvants have been reported to induce both mucosal and systemic immunity when applied to mucosal surfaces and this dual response appears important for protection against certain pathogens. Despite the potential advantages, however, no mucosal adjuvants are currently approved for human use. Evaluating compounds as mucosal adjuvants is a slow and costly process due to the need for lengthy animal immunogenicity studies. We have constructed a library of 112 intranasal adjuvant candidate formulations consisting of oil-in-water nanoemulsions that contain various cationic and nonionic surfactants. To facilitate adjuvant development we first evaluated this library in a series of high-throughput, in vitro assays for activities associated with innate and adaptive immune activation in vivo. These in vitro assays screened for the ability of the adjuvant to bind to mucin, induce cytotoxicity, facilitate antigen uptake in epithelial and dendritic cells, and activate cellular pathways. We then sought to determine how these parameters related to adjuvant activity in vivo. While the in vitro assays alone were not enough to predict the in vivo adjuvant activity completely, several interesting relationships were found with immune responses in mice. Furthermore, by varying the physicochemical properties of the surfactant components (charge, surfactant polar head size and hydrophobicity) and the surfactant blend ratio of the formulations, the strength and type of the immune response generated (TH1, TH2, TH17) could be modulated. These findings suggest the possibility of using high-throughput screens to aid in the design of custom adjuvants with unique immunological profiles to match specific mucosal vaccine applications.
机译:据报道,疫苗佐剂应用于粘膜表面时可诱导粘膜和全身免疫,这种双重应答对于保护抵抗某些病原体似乎很重要。尽管具有潜在的优势,但是,目前尚无任何粘膜佐剂被批准用于人类。由于需要进行长时间的动物免疫原性研究,因此将化合物作为粘膜佐剂进行评估是一个缓慢而昂贵的过程。我们已经建立了一个112种鼻内佐剂候选制剂的资料库,这些制剂由包含各种阳离子和非离子表面活性剂的水包油纳米乳剂组成。为促进佐剂开发,我们首先在一系列高通量的体外测定中评估了该文库的体内与先天和适应性免疫激活相关的活性。这些体外试验筛选了佐剂与粘蛋白结合,诱导细胞毒性,促进上皮和树突状细胞中抗原吸收以及激活细胞途径的能力。然后,我们试图确定这些参数如何与体内佐剂活性相关。尽管仅靠体外试验不足以完全预测体内佐剂的活性,但在小鼠的免疫反应中发现了一些有趣的关系。此外,通过改变表面活性剂组分的物理化学性质(电荷,表面活性剂极性头大小和疏水性)和制剂的表面活性剂混合比例,可以调节所产生的免疫应答的强度和类型(TH1,TH2,TH17)。这些发现暗示了使用高通量筛选来帮助设计具有独特免疫学特征以匹配特定粘膜疫苗应用的定制佐剂的可能性。

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