Tan Ming, Jiang Xi
Division of Infectious Diseases; Cincinnati Children's Hospital Medical Center; Cincinnati, OH USA; Department of Pediatrics; University of Cincinnati College of Medicine; Cincinnati, OH USA.
Hum Vaccin Immunother. 2014;10(6):1449-56. doi: 10.4161/hv.28626. Epub 2014 May 5.
Noroviruses (NoVs) are important pathogens causing epidemic acute gastroenteritis affecting millions of people worldwide. Due to the inability to cultivate NoVs, current NoV vaccine development relies on bioengineering technologies to produce virus-like particles (VLPs) and other subviral particles of NoVs as subunit vaccines. The first VLP vaccine has reached phase II clinical trials and several others are under development in pre-clinical research. Several subviral complexes made from the protruding (P) domains of NoV capsid share common features of easy production, high stability and high immunogenicity and thus are candidates for low cost vaccines. These P domain complexes can also be used as vaccine platforms to present foreign antigens for potential dual vaccines against NoVs and other pathogens. Development of NoV vaccines also faces other challenges, including genetic diversity of NoVs, limit understanding of NoV immunology and evolution, and lack of an efficient NoV animal model for vaccine assessment, which are discussed in this article.
诺如病毒(NoVs)是引起流行性急性肠胃炎的重要病原体,全球数百万人受其影响。由于无法培养诺如病毒,目前诺如病毒疫苗的研发依赖生物工程技术来生产病毒样颗粒(VLPs)和诺如病毒的其他亚病毒颗粒作为亚单位疫苗。首款VLP疫苗已进入II期临床试验,其他几种疫苗正在临床前研究阶段进行开发。由诺如病毒衣壳的突出(P)结构域制成的几种亚病毒复合物具有易于生产、高稳定性和高免疫原性等共同特征,因此是低成本疫苗的候选物。这些P结构域复合物还可作为疫苗平台来呈递外源抗原,用于开发针对诺如病毒和其他病原体的潜在双价疫苗。诺如病毒疫苗的研发还面临其他挑战,包括诺如病毒的基因多样性、对诺如病毒免疫学和进化的了解有限,以及缺乏用于疫苗评估的高效诺如病毒动物模型,本文将对这些问题进行讨论。