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毕赤酵母表达的肠道病毒 D68 病毒样颗粒能有效地诱导中和抗体应答,并赋予小鼠针对致死性病毒感染的保护作用。

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

机构信息

Joint Center for Infection and Immunity, Guangzhou Institute of Pediatrics, Department of Gastroenterology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, 510623, Guangzhou, China.

Unit of Vaccinology & Antiviral Strategies, CAS Key Laboratory of Molecular Virology & Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, 200031, Shanghai, China.

出版信息

Emerg Microbes Infect. 2018 Jan 10;7(1):3. doi: 10.1038/s41426-017-0005-x.

DOI:10.1038/s41426-017-0005-x
PMID:29323105
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5837163/
Abstract

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.

摘要

肠道病毒 D68(EV-D68)在全球范围内与儿童严重呼吸道疾病和神经系统并发症的关联性日益增加。然而,目前尚无预防 EV-D68 感染的疫苗。在本研究中,我们研究了开发基于病毒样颗粒(VLP)的 EV-D68 疫苗的可能性。我们发现,在毕赤酵母中共同表达 EV-D68 的 P1 前体和 3CD 蛋白酶可产生 EV-D68 VLP,其由加工的 VP0、VP1 和 VP3 衣壳蛋白组成,并被视为~30nm 球形颗粒。用这些 VLP 免疫的小鼠产生的血清抗体能够特异性中和体外的 EV-D68 感染。在两项攻毒实验中评估了 EV-D68 VLP 候选疫苗的体内保护效力。第一项攻毒实验表明,来自 VLP 免疫母鼠的新生小鼠完全免受致死性 EV-D68 感染,而在第二项实验中,发现抗-VLP 血清的被动转移可使受体小鼠完全免受感染。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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/86100dee3316/41426_2017_5_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/ef48d2593e37/41426_2017_5_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/aeb85b2e505b/41426_2017_5_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/830b5dcf60fe/41426_2017_5_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/1c628c7e9242/41426_2017_5_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/86100dee3316/41426_2017_5_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/ef48d2593e37/41426_2017_5_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/aeb85b2e505b/41426_2017_5_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/830b5dcf60fe/41426_2017_5_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/1c628c7e9242/41426_2017_5_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d49b/5837163/86100dee3316/41426_2017_5_Fig5_HTML.jpg

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