聚合纳米颗粒工程作为疫苗佐剂递送系统

B. Liu, Zhangbao Wu, Ting Liu, Ruifeng Qian, Tingni Wu, Qingchuan Liu, Aizong Shen
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引用次数: 6

摘要

全球免疫每年通过使用疫苗挽救数百万人的生命,其中包括基于整个微生物的产品和仅由抗原成分配制的亚基产品,这些抗原成分能够刺激免疫系统建立针对疾病的特异性免疫。亚单位疫苗具有许多优点,如成分明确、安全性高、生产时不使用危险病原体,但由于缺乏抗原以外的其他成分,包括能够激活先天免疫反应的病原体相关分子模式的免疫刺激成分,其激发免疫的能力也有限。近年来,由聚乳酸-羟基乙酸、病毒蛋白、壳聚糖、透明质酸和聚苯乙烯等高分子材料配制的纳米颗粒(NPs)具有一定的内在佐剂性,被广泛用作疫苗佐剂递送系统(vads),在亚单位疫苗的开发中显示出巨大的潜力。特别是,用功能材料设计的聚合物NPs具有许多特性,如靶向递送,溶酶体逃逸,抗损伤保护,以及引导免疫反应向Th1 (T辅助型1)和Th2途径的能力,这对于建立体液和细胞免疫至关重要。本章描述了基于聚合np的vads,设计用于开发亚单位疫苗,能够通过不同的接种途径在全身和粘膜水平引发ag特异性免疫。细胞系表达系统[28]。研究人员证明,通过鼻内启动疫苗接种小鼠,然后用脂质体包裹TLR3配体dsRNA佐剂VLPs两次脸颊下刺激,可分泌高滴度的针对Ags的抗体,其中IgG2c多于IgG,并产生显著增加的生发中心B细胞和T滤泡细胞,这表明基于vlp的VADS在诱导th1偏向性免疫应答方面更优越,同时延长淋巴结生发中心。T滤泡细胞,并产生中和抗体,因此非常适合制作HIV疫苗[26]。
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Polymeric Nanoparticles Engineered as a Vaccine Adjuvant-Delivery System
Global immunization saves millions of human lives each year through using vaccines, which include whole microbe-based products and the subunit ones formulated with just the components of antigens able to stimulate immune system to establish specific immunity against diseases. Subunit vaccines show numerous advantages, such as defined components, high safety profile, and production without the use of dangerous pathogens, but also limited capacity in eliciting immunity due to the lack of other components than antigens, including the immunostimulatory elements of pathogen- associated molecular patterns which are able to activate the innate immunoreponses. Recently, nanoparticles (NPs) formulated with polymeric materials, such as poly(lactic- co-glycolic acid), viral proteins, chitosan, hyaluronic acid, and polystyrene, with some bearing intrinsic adjuvanticity, are widely employed as vaccine adjuvant-delivery sys- tems (VADSs) and show great potential in developing subunit vaccines. Particularly, the polymeric NPs engineered with functional materials possess many features, such as targeting delivery, lysosome escape, anti-damaging protection, and ability to guide immune reactions toward a Th1 (T helper type 1) and Th2 pathway, which are crucial for establishing humoral and cellular immunity. This chapter describes polymeric NP-based VADSs designed for developing subunit vaccines able to elicit Ag-specific immunity at both systemic and mucosal levels via different vaccination routes. cell line expression system [28]. The researchers demonstrated that mice vaccinated by intranasal prime followed by two sub-cheek boosts with VLPs adjuvanted with liposomes entrapping TLR3 ligand dsRNA were stimulated to secrete high titers of Abs against the Ags, with predominant IgG2c over IgG and produce a significantly increased germinal center B cells and T follicular cells, suggesting that the VLP-based VADS is superior for induction of a Th1-biased immune response, while prolonging lymph node germinal centers, T follicular cells, and generating neutralizing antibodies, and thus is rather suitable for making HIV vaccines [26].
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Vaccines Developed for Cancer Immunotherapy Polymeric Nanoparticles Engineered as a Vaccine Adjuvant-Delivery System Vaccine Adjuvant Delivery Systems Constructed Using Biocompatible Nanoparticles Formed through Self-Assembly of Small Molecules Introductory Chapter: Immunization - Vaccine Adjuvant Delivery System and Strategies Practical Finance Strategies in Immunization
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