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一种从适应 Vero 细胞的寨卡病毒中纯化的灭活疫苗可在小鼠中引发保护作用。

A purified inactivated vaccine derived from Vero cell-adapted zika virus elicits protection in mice.

机构信息

R&D Center, GeneMatrix, Inc., Seongnam-si, Gyeonggi-do, Republic of Korea.

R&D Center, GeneMatrix, Inc., Seongnam-si, Gyeonggi-do, Republic of Korea.

出版信息

Virology. 2021 Aug;560:124-130. doi: 10.1016/j.virol.2021.05.003. Epub 2021 May 12.

Abstract

The Zika virus (ZIKV) outbreak in 2015-2016 raised public health concerns and created a pressing need for vaccine development. However, no vaccine has been developed and most of the ones under development use a single serotype of ZIKV. In this study, we established a Vero cell-adapted ZIKV strain (GMZ-002) and developed a purified inactivated virus (PIV) vaccine. GMZ-002 presented significantly increased productivity in Vero cells, and IFNAR1-blocked C57BL/6 mice administered two doses of the PIV were fully protected against lethal challenge. Vaccine efficacy was illustrated by the high level of serum neutralizing antibodies and strong innate immune response, along with an absence of detectable viremia in vaccinated mice. Furthermore, anti-sera neutralized both African and Asian genetic lineages of the virus in vitro. Our results suggest that GMZ-002 PIV elicited robust and persistent protective immunity, and therefore represents a promising vaccine candidate for ZIKV.

摘要

2015-2016 年的 Zika 病毒(ZIKV)爆发引起了公众健康的关注,并迫切需要开发疫苗。然而,目前尚无疫苗被开发出来,而且大多数正在开发的疫苗都使用单一血清型的 ZIKV。在本研究中,我们建立了一株适应 Vero 细胞的 Zika 病毒株(GMZ-002),并开发了一种纯化的灭活病毒(PIV)疫苗。GMZ-002 在 Vero 细胞中表现出显著提高的生产能力,用 IFNAR1 阻断的 C57BL/6 小鼠给予两剂 PIV 完全免受致死性挑战的保护。疫苗的功效通过高水平的血清中和抗体和强烈的先天免疫反应来证明,同时接种疫苗的小鼠中没有检测到可检测的病毒血症。此外,抗血清在体外中和了该病毒的非洲和亚洲遗传谱系。我们的结果表明,GMZ-002 PIV 引起了强大和持久的保护免疫,因此代表了 Zika 病毒的一种有前途的候选疫苗。

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