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Enterovirus D68 virus-like particles expressed in Pichia pastoris potently induce neutralizing antibody responses and confer protection against lethal viral infection in mice

机译:在巴斯德毕赤酵母中表达的肠病毒D68病毒样颗粒有效诱导中和抗体反应并赋予小鼠抗致命病毒感染的保护作用

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摘要

Enterovirus D68 (EV-D68) has been increasingly associated with severe respiratory illness and neurological complications in children worldwide. However, no vaccine is currently available to prevent EV-D68 infection. In the present study, we investigated the possibility of developing a virus-like particle (VLP)-based EV-D68 vaccine. We found that co-expression of the P1 precursor and 3CD protease of EV-D68 in Pichia pastoris yeast resulted in the generation of EV-D68 VLPs, which were composed of processed VP0, VP1, and VP3 capsid proteins and were visualized as ~30 nm spherical particles. Mice immunized with these VLPs produced serum antibodies capable of specifically neutralizing EV-D68 infections in vitro. The in vivo protective efficacy of the EV-D68 VLP candidate vaccine was assessed in two challenge experiments. The first challenge experiment showed that neonatal mice born to the VLP-immunized dams were fully protected from lethal EV-D68 infection, whereas in the second experiment, passive transfer of anti-VLP sera was found to confer complete protection in the recipient mice. Collectively, these results demonstrate the proof-of-concept for VLP-based broadly effective EV-D68 vaccines.
机译:肠病毒D68(EV-D68)与世界各地儿童的严重呼吸系统疾病和神经系统并发症越来越相关。但是,目前尚无疫苗可预防EV-D68感染。在本研究中,我们调查了开发基于病毒样颗粒(VLP)的EV-D68疫苗的可能性。我们发现在毕赤酵母中共表达EV-D68的P1前体和3CD蛋白酶导致了EV-D68 VLP的生成,这些VLP由加工后的VP0,VP1和VP3衣壳蛋白组成,可视化为〜30纳米球形颗粒。用这些VLP免疫的小鼠产生的血清抗体能够在体外特异性中和EV-D68感染。在两个挑战性实验中评估了EV-D68 VLP候选疫苗的体内保护功效。第一个挑战实验表明,完全免疫VLP免疫母鼠的新生小鼠免受致命性EV-D68感染,而在第二个实验中,发现抗VLP血清的被动转移可为受体小鼠提供完全保护。总的来说,这些结果证明了基于VLP的广泛有效的EV-D68疫苗的概念验证。

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