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Development of live attenuated Enterovirus 71 vaccine strains that confer protection against lethal challenge in mice

机译:减毒肠病毒71型减毒活疫苗株的开发可赋予小鼠抗致命性攻击的保护

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摘要

Besides causing mild hand, foot and mouth infections, Enterovirus A71 (EV-A71) is associated with neurological complications and fatality. With concerns about rising EV-A71 virulence, there is an urgency for more effective vaccines. The live attenuated vaccine (LAV) is a more valuable vaccine as it can elicit both humoral and cellular immune responses. A miRNA-based vaccine strain (pIY) carrying let-7a and miR-124a target genes in the EV-A71 genome which has a partial deletion in the 5′NTR (∆11 bp) and G64R mutation (3Dp°l) was designed. The viral RNA copy number and viral titers of the pIY strain were significantly lower in SHSY-5Y cells that expressed both let-7a and miR-124a. Inhibition of the cognate miRNAs expressed in RD and SHSY-5Y cells demonstrated de-repression of viral mRNA translation. A previously constructed multiply mutated strain, MMS and the pIY vaccine strain were assessed in their ability to protect 4-week old mice from hind limb paralysis. The MMS showed higher amounts of IFN-γ ex vivo than the pIY vaccine strain. There was absence of EV-A71 antigen in the skeletal muscles and spinal cord micrographs of mice vaccinated with the MMS and pIY strains. The MMS and pIY strains are promising LAV candidates developed against severe EV-A71 infections.
机译:肠病毒A71(EV-A71)除了引起轻度的手足口感染外,还伴有神经系统并发症和死亡。由于担心EV-A71毒力的上升,迫切需要更有效的疫苗。减毒活疫苗(LAV)是一种更有价值的疫苗,因为它可以引起体液和细胞免疫反应。基于miRNA的疫苗株(pIY),在EV-A71基因组中带有let-7a和miR-124a目标基因,该基因在5'NTR(∆11 bp)和G64R突变中有部分缺失(3D p < / sup>° l )。在同时表达let-7a和miR-124a的SHSY-5Y细胞中,pIY株的病毒RNA拷贝数和病毒滴度显着降低。在RD和SHSY-5Y细胞中表达的同源miRNA的抑制显示病毒mRNA翻译的抑制。评估了先前构建的多重突变株,MMS和pIY疫苗株在保护4周龄小鼠后肢瘫痪方面的能力。 MMS显示比pIY疫苗株更高的离体IFN-γ量。接种MMS和pIY株的小鼠的骨骼肌和脊髓显微照片中没有EV-A71抗原。 MMS和pIY菌株有望开发出抗严重EV-A71感染的LAV候选药物。

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