J Clin Invest. 2019 Apr 15;129(5):1836-1838. doi: 10.1172/JCI128370.
The Epstein-Barr virus (EBV) is estimated to infect a large part of the population and is associated with a variety of human tumors; therefore, EBV is an important target for vaccine development. In this issue of the JCI, Rühl et al. developed a promising heterologous prime-boost vaccination strategy for EBV-associated malignancies and symptomatic primary infection. The authors show that two prime-boost regimens, using either dendritic cells or an adenovirus approach targeting nuclear antigen EBNA1 followed by a modified vaccinia virus Ankara (MVA) booster, induced significant T cell-mediated, EBV-specific immune control and Ab production. These findings suggest that administration of heterologous prime-boost vaccinations targeting EBNA1 may result in potent CD4+ and CD8+ T cell-mediated EBV immune control and may be a promising clinical approach.
EB 病毒(EBV)估计会感染很大一部分人群,并与多种人类肿瘤相关;因此,EBV 是疫苗开发的一个重要目标。在本期 JCI 中,Rühl 等人针对 EBV 相关恶性肿瘤和有症状的原发性感染,开发了一种很有前途的异源初免-加强免疫接种策略。作者表明,两种初免-加强免疫方案,一种使用树突细胞,另一种使用针对核抗原 EBNA1 的腺病毒方法,继之以改良安卡拉牛痘病毒(MVA)加强剂,可诱导显著的 T 细胞介导的、针对 EBV 的免疫控制和 Ab 产生。这些发现表明,针对 EBNA1 的异源初免-加强免疫接种的施用可能会导致有效的 CD4+和 CD8+T 细胞介导的 EBV 免疫控制,并且可能是一种很有前途的临床方法。