School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, 1211 Geneva, Switzerland.
Mol Pharm. 2013 May 6;10(5):1596-609. doi: 10.1021/mp300597g. Epub 2013 Apr 24.
Mucosal immunization offers the promises of eliciting a systemic and mucosal immune response, as well as enhanced patient compliance. Mucosal vaccination using defined antigens such as proteins and peptides requires delivery systems that combine good safety profiles with strong immunogenicity, which may be provided by virus-like particles (VLP). VLP are assembled from viral structural proteins and thus are devoid of any genetic material. They excel by mimicking natural pathogens, therefore providing antigen-protecting particulate nature, inherent immune-cell stimulatory mechanisms, and tissue-specific targeting depending on their parental virus. Nevertheless, despite of promising preclinical results, VLP remain rarely investigated in clinical studies. This review is intended to give an overview of obstacles and promises of VLP-based mucosal immunization as well as to identify strategies to further improve VLP while maintaining a good safety and tolerability profile.
黏膜免疫接种具有激发系统和黏膜免疫应答以及提高患者依从性的潜力。使用蛋白质和肽等定义抗原进行黏膜疫苗接种需要结合良好的安全性和强大的免疫原性的递送系统,这可以通过病毒样颗粒(VLPs)来提供。VLPs 由病毒结构蛋白组装而成,因此不含任何遗传物质。它们通过模拟天然病原体而表现出色,因此提供抗原保护的颗粒性质、固有免疫细胞刺激机制以及根据其亲本病毒的组织特异性靶向性。然而,尽管有有前景的临床前结果,但 VLPs 在临床研究中仍很少被研究。本文旨在概述基于 VLPs 的黏膜免疫接种的障碍和前景,并确定进一步改善 VLPs 的策略,同时保持良好的安全性和耐受性。