Kilgore Paul B, Sha Jian, Andersson Jourdan A, Motin Vladimir L, Chopra Ashok K
Department of Microbiology & Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Institute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, TX, USA.
NPJ Vaccines. 2021 Jan 29;6(1):21. doi: 10.1038/s41541-020-00275-3.
A plague vaccine with a fusion cassette of YscF, F1, and LcrV encoding genes in an adenovirus-5 vector (rAd5-YFV) is evaluated for efficacy and immune responses in mice. Two doses of the vaccine provides 100% protection when administered intranasally against challenge with Yersinia pestis CO92 or its isogenic F1 mutant in short- or long- term immunization in pneumonic/bubonic plague models. The corresponding protection rates drop in rAd5-LcrV monovalent vaccinated mice in plague models. The rAd5-YFV vaccine induces superior humoral, mucosal and cell-mediated immunity, with clearance of the pathogen. Immunization of mice with rAd5-YFV followed by CO92 infection dampens proinflammatory cytokines and neutrophil chemoattractant production, while increasing Th1- and Th2-cytokine responses as well as macrophage/monocyte chemo-attractants when compared to the challenge control animals. This is a first study showing complete protection of mice from pneumonic/bubonic plague with a viral vector-based vaccine without the use of needles and the adjuvant.
一种腺病毒5型载体(rAd5-YFV)中含有编码YscF、F1和LcrV基因的融合盒的鼠疫疫苗,在小鼠中进行了疗效和免疫反应评估。在肺炎/腺鼠疫模型的短期或长期免疫中,经鼻内给药两剂该疫苗,可提供100%的保护,抵御鼠疫耶尔森菌CO92或其同基因F1突变体的攻击。在鼠疫模型中,rAd5-LcrV单价疫苗接种小鼠的相应保护率下降。rAd5-YFV疫苗可诱导卓越的体液免疫、黏膜免疫和细胞介导免疫,并清除病原体。与攻击对照动物相比,用rAd5-YFV免疫小鼠后再感染CO92,可抑制促炎细胞因子和中性粒细胞趋化因子的产生,同时增加Th1和Th2细胞因子反应以及巨噬细胞/单核细胞趋化因子。这是第一项表明基于病毒载体的疫苗无需使用针头和佐剂即可完全保护小鼠免受肺炎/腺鼠疫感染的研究。