鼻腔内接种由 NDV 病毒侵染的 SARS-CoV-2 疫苗可抵御 Delta 和 Omicron 的挑战。

IF 6.9 1区 医学 Q1 IMMUNOLOGY NPJ Vaccines Pub Date : 2024-05-23 DOI:10.1038/s41541-024-00870-8
Bryce M Warner, Jacob G E Yates, Robert Vendramelli, Thang Truong, Courtney Meilleur, Lily Chan, Alexander Leacy, Phuc H Pham, Yanlong Pei, Leonardo Susta, Sarah K Wootton, Darwyn Kobasa
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引用次数: 0

摘要

据估计,严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)出现后,疫苗的快速开发和部署挽救了数百万人的生命。尽管取得了巨大成功,但仍需要针对 SARS-CoV-2 和未来新出现的冠状病毒及其他呼吸道病毒的下一代疫苗接种方法。在这里,我们使用了一种新城疫病毒(NDV)载体疫苗,该疫苗以预融合稳定嵌合构象(NDV-PFS)表达 SARS-CoV-2 的祖先尖峰蛋白。经鼻给药后,NDV-PFS 可保护叙利亚仓鼠和 K18 小鼠免受 SARS-CoV-2 Delta 和 Omicron 变体的感染。此外,鼻内接种疫苗还能产生强效、持久的保护作用,并可延长至接种后 6 个月。总之,我们的数据证明,NDV载体疫苗是一种可行的下一代粘膜疫苗接种方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Intranasal vaccination with an NDV-vectored SARS-CoV-2 vaccine protects against Delta and Omicron challenges.

The rapid development and deployment of vaccines following the emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been estimated to have saved millions of lives. Despite their immense success, there remains a need for next-generation vaccination approaches for SARS-CoV-2 and future emerging coronaviruses and other respiratory viruses. Here we utilized a Newcastle Disease virus (NDV) vectored vaccine expressing the ancestral SARS-CoV-2 spike protein in a pre-fusion stabilized chimeric conformation (NDV-PFS). When delivered intranasally, NDV-PFS protected both Syrian hamsters and K18 mice against Delta and Omicron SARS-CoV-2 variants of concern. Additionally, intranasal vaccination induced robust, durable protection that was extended to 6 months post-vaccination. Overall, our data provide evidence that NDV-vectored vaccines represent a viable next-generation mucosal vaccination approach.

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来源期刊
NPJ Vaccines
NPJ Vaccines Immunology and Microbiology-Immunology
CiteScore
11.90
自引率
4.30%
发文量
146
审稿时长
11 weeks
期刊介绍: Online-only and open access, npj Vaccines is dedicated to highlighting the most important scientific advances in vaccine research and development.
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