Cimica Velasco, Galarza Jose M
TechnoVax, Inc., 765 Old Saw Mill River Road, Tarrytown, NY 10591, United States.
TechnoVax, Inc., 765 Old Saw Mill River Road, Tarrytown, NY 10591, United States.
Clin Immunol. 2017 Oct;183:99-108. doi: 10.1016/j.clim.2017.08.004. Epub 2017 Aug 3.
The development of virus-like particle (VLP) technology has had an enormous impact on modern vaccinology. In order to optimize the efficacy and safety of VLP-based vaccines, adjuvants are included in most vaccine formulations. To date, most licensed VLP-based vaccines utilize the classic aluminum adjuvant compositions. Certain challenging pathogens and weak immune responder subjects may require further optimization of the adjuvant formulation to maximize the magnitude and duration of the protective immunity. Indeed, novel classes of adjuvants such as liposomes, agonists of pathogen recognition receptors, polymeric particles, emulsions, cytokines and bacterial toxins, can be used to further improve the immunostimulatory activity of a VLP-based vaccine. This review describes the current advances in adjuvant technology for VLP-based vaccines directed at viral diseases, and discusses the basic principles for designing adjuvant formulations for enhancing the vaccine immunogenicity.
病毒样颗粒(VLP)技术的发展对现代疫苗学产生了巨大影响。为了优化基于VLP的疫苗的效力和安全性,大多数疫苗配方中都包含佐剂。迄今为止,大多数已获许可的基于VLP的疫苗都采用经典的铝佐剂组合物。某些具有挑战性的病原体和免疫反应较弱的受试者可能需要进一步优化佐剂配方,以最大限度地提高保护性免疫的强度和持续时间。事实上,新型佐剂,如脂质体、病原体识别受体激动剂、聚合物颗粒、乳剂、细胞因子和细菌毒素,可用于进一步提高基于VLP的疫苗的免疫刺激活性。本文综述了针对病毒性疾病的基于VLP的疫苗佐剂技术的当前进展,并讨论了设计增强疫苗免疫原性的佐剂配方的基本原理。