Suppr超能文献

含 SARS-CoV-2 刺突蛋白和 H5N1 基质 1 蛋白的嵌合病毒样颗粒的免疫原性和保护潜力。

Immunogenicity and protective potential of chimeric virus-like particles containing SARS-CoV-2 spike and H5N1 matrix 1 proteins.

机构信息

College of Veterinary medicine, Key Lab for Zoonoses Research, Ministry of Education, Jilin University, Changchun, China.

Research Unit of Key Technologies for Prevention and Control of Virus Zoonoses, Chinese Academy of Medical Sciences, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.

出版信息

Front Cell Infect Microbiol. 2022 Jul 18;12:967493. doi: 10.3389/fcimb.2022.967493. eCollection 2022.

Abstract

Coronavirus Disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2), has posed a constant threat to human beings and the world economy for more than two years. Vaccination is the first choice to control and prevent the pandemic. However, an effective SARS-CoV-2 vaccine against the virus infection is still needed. This study designed and prepared four kinds of virus-like particles (VLPs) using an insect expression system. Two constructs encoded wild-type SARS-CoV-2 spike (S) fused with or without H5N1 matrix 1 (M1) (S and SM). The other two constructs contained a codon-optimized spike gene and/or M1 gene (mS and mSM) based on protein expression, stability, and ADE avoidance. The results showed that the VLP-based vaccine could induce high SARS-CoV-2 specific antibodies in mice, including specific IgG, IgG1, and IgG2a. Moreover, the mSM group has the most robust ability to stimulate humoral immunity and cellular immunity than the other VLPs, suggesting the mSM is the best immunogen. Further studies showed that the mSM combined with Al/CpG adjuvant could stimulate animals to produce sustained high-level antibodies and establish an effective protective barrier to protect mice from challenges with mouse-adapted strain. The vaccine based on mSM and Al/CpG adjuvant is a promising candidate vaccine to prevent the COVID-19 pandemic.

摘要

新型冠状病毒病(COVID-19)由严重急性呼吸系统综合征冠状病毒 2 型(SARS-CoV-2)引起,已对人类和世界经济造成两年多的持续威胁。疫苗接种是控制和预防大流行的首选方法。然而,仍然需要针对病毒感染的有效 SARS-CoV-2 疫苗。本研究使用昆虫表达系统设计并制备了四种病毒样颗粒(VLPs)。两种构建体编码野生型 SARS-CoV-2 刺突(S)与或不与 H5N1 基质 1(M1)融合(S 和 SM)。另外两种构建体包含基于蛋白表达、稳定性和避免 ADE 的优化密码子刺突基因和/或 M1 基因(mS 和 mSM)。结果表明,基于 VLP 的疫苗可在小鼠中诱导高 SARS-CoV-2 特异性抗体,包括特异性 IgG、IgG1 和 IgG2a。此外,mSM 组比其他 VLPs 更能刺激体液免疫和细胞免疫,表明 mSM 是最佳免疫原。进一步的研究表明,mSM 与 Al/CpG 佐剂联合使用可以刺激动物产生持续高水平的抗体,并建立有效的保护屏障,保护小鼠免受鼠适应株的挑战。基于 mSM 和 Al/CpG 佐剂的疫苗是预防 COVID-19 大流行的有前途的候选疫苗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验