Viral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Institute for Systems Biology, Seattle, WA 98109, USA.
Sci Transl Med. 2022 Jul 13;14(653):eabo2167. doi: 10.1126/scitranslmed.abo2167.
Influenza A viruses (IAVs) present major public health threats from annual seasonal epidemics and pandemics and from viruses adapted to a variety of animals including poultry, pigs, and horses. Vaccines that broadly protect against all such IAVs, so-called "universal" influenza vaccines, do not currently exist but are urgently needed. Here, we demonstrated that an inactivated, multivalent whole-virus vaccine, delivered intramuscularly or intranasally, was broadly protective against challenges with multiple IAV hemagglutinin and neuraminidase subtypes in both mice and ferrets. The vaccine is composed of four β-propiolactone-inactivated low-pathogenicity avian IAV subtypes of H1N9, H3N8, H5N1, and H7N3. Vaccinated mice and ferrets demonstrated substantial protection against a variety of IAVs, including the 1918 H1N1 strain, the highly pathogenic avian H5N8 strain, and H7N9. We also observed protection against challenge with antigenically variable and heterosubtypic avian, swine, and human viruses. Compared to control animals, vaccinated mice and ferrets demonstrated marked reductions in viral titers, lung pathology, and host inflammatory responses. This vaccine approach indicates the feasibility of eliciting broad, heterosubtypic IAV protection and identifies a promising candidate for influenza vaccine clinical development.
甲型流感病毒(IAV)每年都会引发季节性流行和大流行,对公共健康构成重大威胁,还会由适应各种动物(包括家禽、猪和马)的病毒引发。目前尚无广泛预防所有此类 IAV 的疫苗,即所谓的“通用”流感疫苗,但却急需这样的疫苗。在这里,我们证明了一种灭活的、多价全病毒疫苗,通过肌肉内或鼻内给药,可在小鼠和雪貂中广泛预防多种 IAV 血凝素和神经氨酸酶亚型的挑战。该疫苗由四种β-丙内酯灭活的低致病性禽源 IAV 亚型 H1N9、H3N8、H5N1 和 H7N3 组成。接种疫苗的小鼠和雪貂对多种 IAV 表现出显著的保护作用,包括 1918 年 H1N1 株、高致病性禽源 H5N8 株和 H7N9 株。我们还观察到对具有抗原变异性和异源亚型的禽源、猪源和人源病毒的保护作用。与对照动物相比,接种疫苗的小鼠和雪貂的病毒滴度、肺部病理和宿主炎症反应明显降低。这种疫苗方法表明,激发广泛的、异源亚型 IAV 保护是可行的,并确定了流感疫苗临床开发的有希望的候选者。