用鼻内新城疫病毒(NDV)为基础的XBB.1.5变异疫苗进行单次免疫,可减少动物在对抗匹配变异攻击时的疾病和传播。

IF 4.5 3区 医学 Q2 IMMUNOLOGY Vaccine Pub Date : 2025-01-25 DOI:10.1016/j.vaccine.2024.126586
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。
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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.
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
期刊最新文献
Socio-demographic differences in citizen' preferences for distributing a scarce, lifesaving resource: A case study using COVID-19 vaccine distribution in Belgium Anti-vaccine attitudes and COVID-19 vaccine status at the end of the U.S. public health emergency Influenza vaccine effectiveness in Iceland 2014–2022: A test-negative design Meeting report: CEPI workshop on Rift Valley fever epidemiology and modeling to inform human vaccine development, Nairobi, 4–5 June 2024 A phase I study of the safety, reactogenicity and immunogenicity of two quadrivalent seasonal influenza vaccines (Fluzone® or Flublok®) with or without one of two adjuvants (AF03 or Advax-CpG55.2) in healthy adults 18–45 years of age
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