Suppr超能文献

合成多抗原痘苗病毒载体疫苗COH04S1可保护叙利亚仓鼠和非人类灵长类动物免受新冠病毒感染。

Synthetic Multiantigen MVA Vaccine COH04S1 Protects Against SARS-CoV-2 in Syrian Hamsters and Non-Human Primates.

作者信息

Chiuppesi Flavia, Nguyen Vu H, Park Yoonsuh, Contreras Heidi, Karpinski Veronica, Faircloth Katelyn, Nguyen Jenny, Kha Mindy, Johnson Daisy, Martinez Joy, Iniguez Angelina, Zhou Qiao, Kaltcheva Teodora, Frankel Paul, Kar Swagata, Sharma Ankur, Andersen Hanne, Lewis Mark G, Shostak Yuriy, Wussow Felix, Diamond Don J

出版信息

bioRxiv. 2021 Sep 15:2021.09.15.460487. doi: 10.1101/2021.09.15.460487.

Abstract

Second-generation COVID-19 vaccines could contribute to establish protective immunity against SARS-CoV-2 and its emerging variants. We developed COH04S1, a synthetic multiantigen Modified Vaccinia Ankara-based SARS-CoV-2 vaccine that co-expresses spike and nucleocapsid antigens. Here, we report COH04S1 vaccine efficacy in animal models. We demonstrate that intramuscular or intranasal vaccination of Syrian hamsters with COH04S1 induces robust Th1-biased antigen-specific humoral immunity and cross-neutralizing antibodies (NAb) and protects against weight loss, lower respiratory tract infection, and lung injury following intranasal SARS-CoV-2 challenge. Moreover, we demonstrate that single-dose or two-dose vaccination of non-human primates with COH04S1 induces robust antigen-specific binding antibodies, NAb, and Th1-biased T cells, protects against both upper and lower respiratory tract infection following intranasal/intratracheal SARS-CoV-2 challenge, and triggers potent post-challenge anamnestic antiviral responses. These results demonstrate COH04S1-mediated vaccine protection in animal models through different vaccination routes and dose regimens, complementing ongoing investigation of this multiantigen SARS-CoV-2 vaccine in clinical trials.

摘要

第二代新冠疫苗有助于建立针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)及其新出现变体的保护性免疫。我们研发了COH04S1,这是一种基于安卡拉痘苗病毒的合成多抗原新冠疫苗,可共表达刺突蛋白和核衣壳抗原。在此,我们报告COH04S1疫苗在动物模型中的疗效。我们证明,用COH04S1对叙利亚仓鼠进行肌肉注射或鼻内接种可诱导强烈的以Th1为主的抗原特异性体液免疫和交叉中和抗体(NAb),并在鼻内接种SARS-CoV-2后预防体重减轻、下呼吸道感染和肺损伤。此外,我们证明,用COH04S1对非人灵长类动物进行单剂量或两剂量接种可诱导强烈的抗原特异性结合抗体、NAb和以Th1为主的T细胞,在鼻内/气管内接种SARS-CoV-2后预防上呼吸道和下呼吸道感染,并触发强烈的攻毒后回忆性抗病毒反应。这些结果证明了COH04S1通过不同的接种途径和剂量方案在动物模型中介导疫苗保护作用,为正在进行的这种多抗原新冠疫苗的临床试验研究提供了补充。

相似文献

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