Liu Ying, Deng Shaofeng, Ren Shuang, Tam Rachel Chun-Yee, Liu Siwen, Zhang Anna Jinxia, To Kelvin Kai-Wang, Yuen Kwok-Yung, Chen Honglin, Wang Pui
State Key Laboratory for Emerging Infectious Diseases and Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Centre for Virology, Vaccinology and Therapeutics Limited, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Nat Commun. 2025 Apr 1;16(1):3133. doi: 10.1038/s41467-025-58504-z.
The highly pathogenic avian influenza (HPAI) H5N1 virus has been endemic in aquatic birds since 1997, causing outbreaks in domestic poultry and occasional human infections worldwide. Recently, the cross-species transmission of a new reassortant variant from clade 2.3.4.4b of H5N1 to cattle in the US has heightened concerns regarding the expansion of host range and potential human infection. As eradicating the H5N1 virus from its reservoir is impossible, it is essential to prepare for a potential pandemic caused by an H5N1 derivative. Utilizing a deleted-NS1 live attenuated influenza viral vector vaccine system (DelNS1 LAIV), a system we have previously used in the development of a COVID-19 vaccine, we have rapidly developed an intranasal vaccine for cattle H5N1 and related clade 2.3.4.4b strains, based on publicly available sequences. Our research demonstrates that a single intranasal immunization can provide effective protection against lethal challenges from HPAI cattle or mink H5N1 variants, offering strong, sustained immunity after two months in female mouse and male hamster models. Immunogenicity analysis reveals that intranasal vaccination with DelNS1 LAIV induces robust neutralizing antibody, mucosal IgA and T cell responses in mice. It is crucial to further evaluate the DelNS1-H5N1 LAIV system to prepare for potential future H5N1 outbreaks in humans.
自1997年以来,高致病性禽流感(HPAI)H5N1病毒在家水禽中呈地方性流行,在全球范围内导致家禽疫情爆发和偶发的人类感染。最近,H5N1 2.3.4.4b分支的一种新的重组变体跨物种传播至美国的牛,这加剧了人们对宿主范围扩大和潜在人类感染的担忧。由于从其宿主中根除H5N1病毒是不可能的,因此为H5N1衍生病毒可能引发的大流行做好准备至关重要。利用一种缺失NS1的减毒活流感病毒载体疫苗系统(DelNS1 LAIV),这是我们之前在开发COVID-19疫苗时使用过的系统,我们基于公开可用序列,迅速开发出一种用于牛H5N1及相关2.3.4.4b分支毒株的鼻内疫苗。我们的研究表明,单次鼻内免疫可有效抵御高致病性禽流感牛或水貂H5N1变体的致死性攻击,在雌性小鼠和雄性仓鼠模型中两个月后可提供强大、持久的免疫力。免疫原性分析显示,用DelNS1 LAIV进行鼻内疫苗接种可在小鼠体内诱导强大的中和抗体、粘膜IgA和T细胞反应。进一步评估DelNS1-H5N1 LAIV系统对于为未来人类可能爆发的H5N1疫情做好准备至关重要。