Cai Jing, Zhang Bodou, Li Yuqi, Zhu Wanfang, Akihisa Toshihiro, Li Wei, Kikuchi Takashi, Liu Wenyuan, Feng Feng, Zhang Jie
School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, China.
School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China.
Vaccines (Basel). 2021 Nov 7;9(11):1290. doi: 10.3390/vaccines9111290.
The Epstein-Barr virus (EBV) infects more than 95% of adults worldwide and is associated with various malignant tumors and immune diseases, imparting a huge disease burden on the human population. Available EBV vaccines are imminent. Prophylactic vaccines can effectively prevent the spread of infection, whereas therapeutic vaccines mainly stimulate cell-mediated immunity and kill infected cells, thus curbing the development of malignant tumors. Nevertheless, there are still no approved EBV vaccines after decades of effort. The complexity of the EBV life cycle, the lack of appropriate animal models, and the limited reports on adjuvant selection and immune responses are gravely impeding progress in EBV vaccines. The soluble gp350 vaccine could reduce the incidence of infectious mononucleosis (IM), which seemed to offer hope, but could not prevent EBV infection. Continuous research and vaccine trials provide deep insights into the structural biology of viruses, the designs for immunogenicity, and the evolving vaccine platforms. Moreover, the new vaccine candidates are expected to achieve further success via combined immunization to elicit both a dual protection of B cells and epithelial cells, and sustainable immunization against infected cells at several phases of infection.
爱泼斯坦-巴尔病毒(EBV)感染了全球超过95%的成年人,并与多种恶性肿瘤和免疫疾病相关,给人类带来了巨大的疾病负担。可用的EBV疫苗即将问世。预防性疫苗可有效预防感染传播,而治疗性疫苗主要刺激细胞介导的免疫并杀死受感染细胞,从而遏制恶性肿瘤的发展。然而,经过数十年的努力,仍没有获批的EBV疫苗。EBV生命周期的复杂性、缺乏合适的动物模型以及关于佐剂选择和免疫反应的报道有限,严重阻碍了EBV疫苗的研发进展。可溶性gp350疫苗可降低传染性单核细胞增多症(IM)的发病率,这似乎带来了希望,但无法预防EBV感染。持续的研究和疫苗试验为病毒的结构生物学、免疫原性设计以及不断发展的疫苗平台提供了深刻见解。此外,新的候选疫苗有望通过联合免疫实现进一步成功,从而在感染的多个阶段引发对B细胞和上皮细胞的双重保护以及对受感染细胞的持续免疫。