Xiang Sue D, Scholzen Anja, Minigo Gabriela, David Cassandra, Apostolopoulos Vasso, Mottram Patricia L, Plebanski Magdalena
Vaccine and Infectious Diseases Laboratory, Burnet Institute at Austin, Studley Road, Heidelberg, Vic. 3084, Australia.
Methods. 2006 Sep;40(1):1-9. doi: 10.1016/j.ymeth.2006.05.016.
The use of particulate carriers holds great promise for the development of effective and affordable recombinant vaccines. Rational development requires a detailed understanding of particle up-take and processing mechanisms to target cellular pathways capable of stimulating the required immune responses safely. These mechanisms are in turn based on how the host has evolved to recognize and process pathogens. Pathogens, as well as particulate vaccines, come in a wide range of sizes and biochemical compositions. Some of these also provide 'danger signals' so that antigen 'senting cells (APC), usually dendritic cells (DC), acquire specific stimulatory activity. Herein, we provide an overview of the types of particles currently under investigation for the formulation of vaccines, discuss cellular uptake mechanisms (endocytosis, macropinocytosis, phagocytosis, clathrin-dependent and/or caveloae-mediated) for pathogens and particles of different sizes, as well as antigen possessing and presentation by APC in general, and DC in particular. Since particle size and composition can influence the immune response, inducing humoral and/or cellular immunity, activating CD8 T cells and/or CD4 T cells of T helper 1 and/or T helper 2 type, particle characteristics have a major impact on vaccine efficacy. Recently developed methods for the formulation of particulate vaccines are presented in this issue of Methods, showcasing a range of "cutting edge" particulate vaccines that employ particles ranging from nano to micro-sized. This special issue of Methods further addresses practical issues of production, affordability, reproducibility and stability of formulation, and also includes a discussion of the economic and regulatory challenges encountered in developing vaccines for veterinary use and for common Third World infectious diseases.
使用颗粒载体对开发有效且经济实惠的重组疫苗具有巨大潜力。合理的开发需要详细了解颗粒摄取和加工机制,以靶向能够安全刺激所需免疫反应的细胞途径。这些机制又基于宿主如何进化以识别和处理病原体。病原体以及颗粒疫苗具有多种大小和生化组成。其中一些还提供“危险信号”,以便抗原呈递细胞(APC),通常是树突状细胞(DC),获得特定的刺激活性。在此,我们概述了目前正在研究用于疫苗制剂的颗粒类型,讨论了针对不同大小的病原体和颗粒的细胞摄取机制(内吞作用、巨吞饮作用、吞噬作用、网格蛋白依赖性和/或小窝介导的),以及一般情况下APC特别是DC的抗原摄取和呈递。由于颗粒大小和组成可以影响免疫反应,诱导体液和/或细胞免疫,激活CD8 T细胞和/或T辅助1型和/或T辅助2型的CD4 T细胞,颗粒特性对疫苗效力有重大影响。本期《方法》介绍了最近开发的颗粒疫苗制剂方法,展示了一系列“前沿”颗粒疫苗,这些疫苗采用从纳米到微米大小不等的颗粒。《方法》的这一特刊进一步探讨了生产、可承受性、可重复性和制剂稳定性等实际问题,还包括对开发兽用疫苗和常见的第三世界传染病疫苗时遇到的经济和监管挑战的讨论。