Stefan Slamanig, Nicholas Lemus, Tsoi Ying Lai, Gagandeep Singh, Mitali Mishra, Adam Abdeljawad, Marta Boza, Victoria Dolange, Gagandeep Singh, Benhur Lee, Irene González-Domínguez, Michael Schotsaert, Florian Krammer, Peter Palese, Weina Sun
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引用次数: 0
摘要
2019冠状病毒病(COVID-19)疫苗的快速开发有助于减轻大流行的初步影响。然而,为了降低传播率和保护更脆弱和免疫功能低下的个体,无法进行有效的免疫应答,开发下一代粘膜疫苗是必要的。在这里,我们开发了一种基于鼻内新城疫病毒(NDV)的疫苗,该疫苗表达了稳定在融合前构象(NDV- hxp - s)的XBB.1.5变异体的spike。我们证明,用表达XBB.1.5刺突的活NDV-HXP-S进行一次或两次鼻内免疫可诱导小鼠全身和粘膜抗体反应,并保护它们免受XBB.1.5变体严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的攻击。此外,一次或两次鼻内接种ndv - hps - s XBB.1.5可保护仓鼠免受变异匹配感染并减少病毒排放,从而为直接接触传播研究中的naïve动物提供完全保护。本研究显示的数据支持这样一种观点,即鼻内接种变异适应的NDV-HXP-S疫苗可诱导保护性粘膜免疫并降低传播率,突出了单次粘膜疫苗对小鼠和仓鼠的强大保护作用。
A single immunization with intranasal Newcastle disease virus (NDV)-based XBB.1.5 variant vaccine reduces disease and transmission in animals against matched-variant challenge.
The rapid development of coronavirus disease 2019 (COVID-19) vaccines has helped mitigate the initial impact of the pandemic. However, in order to reduce transmission rates and protect more vulnerable and immunocompromised individuals unable to mount an effective immune response, development of a next-generation of mucosal vaccines is necessary. Here, we developed an intranasal Newcastle disease virus (NDV)-based vaccine expressing the spike of the XBB.1.5 variant stabilized in its pre-fusion conformation (NDV-HXP-S). We demonstrated that one or two intranasal immunizations with live NDV-HXP-S expressing the XBB.1.5 spike induces systemic and mucosal antibody responses in mice and protects them from a challenge with the XBB.1.5 variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Furthermore, one or two intranasal vaccinations with NDV-HXP-S XBB.1.5 protected hamsters from variant matched infection and reduced virus emission, thereby providing complete protection to naïve animals in a direct contact transmission study. The data shown in this study supports the notion that intranasal vaccination with variant-adapted NDV-HXP-S induces protective mucosal immunity and reduces transmission rates, highlighting the robust protective efficacy of a single mucosal vaccination in mice and hamsters.