First Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg.
German Center for Infection Research, partner site Hamburg-Lübeck-Borstel-Riems.
J Infect Dis. 2019 Jan 29;219(4):556-561. doi: 10.1093/infdis/jiy565.
In response to the Ebola virus (EBOV) crisis of 2013-2016, a recombinant vesicular stomatitis virus (VSV)-based EBOV vaccine was clinically tested (NCT02283099). A single-dose regimen of VSV-EBOV revealed a safe and immunogenic profile and demonstrated clinical efficacy. While EBOV-specific immune responses to this candidate vaccine have previously been investigated, limited human data on immunity to the VSV vector are available. Within the scope of a phase 1 study, we performed a comprehensive longitudinal analysis of adaptive immune responses to internal VSV proteins following VSV-EBOV immunization. While no preexisting immunity to the vector was observed, more than one-third of subjects developed VSV-specific cytotoxic T-lymphocyte responses and antibodies.
针对 2013-2016 年的埃博拉病毒(EBOV)危机,一种基于重组水疱性口炎病毒(VSV)的 EBOV 疫苗进行了临床测试(NCT02283099)。VSV-EBOV 的单剂方案显示出安全和免疫原性特征,并显示出临床疗效。虽然此前已经研究了这种候选疫苗的 EBOV 特异性免疫反应,但有关对 VSV 载体的免疫的人类数据有限。在一项 1 期研究的范围内,我们对 VSV-EBOV 免疫后针对内部 VSV 蛋白的适应性免疫反应进行了全面的纵向分析。虽然未观察到对载体的预先存在的免疫,但超过三分之一的受试者产生了 VSV 特异性细胞毒性 T 淋巴细胞反应和抗体。