壳聚糖基颗粒作为多肽和蛋白基疫苗的生物相容性递送载体

Brendon Y. Chu , Mohammad Al Kobiasi , Weiguang Zeng , David Mainwaring , David C. Jackson
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引用次数: 11

摘要

人们越来越认识到,聚合物颗粒大小对颗粒疫苗与抗原提呈细胞(APCs)的相互作用有深远影响,从而影响和调节随后的免疫反应。为了开发基于壳聚糖颗粒的免疫避孕疫苗,我们比较了壳聚糖纳米颗粒和微颗粒作为基于黄体生成素释放激素(LHRH)的候选疫苗的递送载体的使用。两种类型的颗粒都被树突状细胞有效地吸收,效果相似。接种含有共轭肽或蛋白质微粒的纳米和微粒也可诱导高水平的lhrh特异性抗体。在蛋白质结合颗粒的情况下,引发的抗体水平与接种完全弗氏佐剂乳化的抗原后引发的抗体水平相似。我们在这里描述的疫苗设计方法可能是诱导针对微生物、病毒和致瘤蛋白抗原的免疫反应的另一种有用方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chitosan-based particles as biocompatible delivery vehicles for peptide and protein-based vaccines

It has become increasingly recognized that polymer particle size can have a profound effect on the interactions of particle-based vaccines with antigen presenting cells (APCs) thereby influencing and modulating ensuing immune responses.With the aim of developing chitosan particle-based immunocontraceptive vaccines, we have compared the use of chitosan nano- and microparticles as delivery vehicles for vaccine candidates based on luteinising hormone-releasing hormone (LHRH). Both particle types were taken up effectively by dendritic cells with similar efficacies. Inoculation with nanoand microparticles containing conjugated peptide or protein microparticles also resulted in the induction of high levels of LHRH-specific antibodies. In the case of protein-conjugated particles, the levels of antibodies elicited were similar to those elicited following inoculation with antigen emulsified with complete Freund's adjuvant. The approach to vaccine design that we have described here could represent another useful method for inducing immune responses against microbial, viral and tumorigenic protein antigens.

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