Nebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
School of Veterinary Medicine and Biomedical Sciences and Nebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
mSphere. 2024 Aug 28;9(8):e0028324. doi: 10.1128/msphere.00283-24. Epub 2024 Aug 1.
In 2009, a novel swine-origin H1N1 virus emerged, causing a pandemic. The virus, known as H1N1pdm09, quickly displaced the circulating H1 lineage and became the dominant seasonal influenza A virus subtype infecting humans. Human-to-swine spillovers of the H1N1pdm09 have occurred frequently, and each occurrence has led to sustained transmission of the human-origin H1N1pdm09 within swine populations. In the present study, we developed a lipid nanoparticle-based DNA vaccine (LNP-DNA) containing the hemagglutinin gene of a swine-origin H1N1pdm09. In pigs, this LNP-DNA vaccine induced a robust antibody response after a single intramuscular immunization and protected the pigs against challenge infection with the homologous swine-origin H1N1pdm09 virus. In a mouse model, the LNP-DNA vaccine induced antibody and T-cell responses and protected mice against lethal challenge with a mouse-adapted human-origin H1N1pdm09 virus. These findings demonstrate the potential of the LNP-DNA vaccine to protect against both swine- and human-origin H1N1pdm09 viruses.
Swine influenza A virus (IAV) is widespread and causes significant economic losses to the swine industry. Moreover, bidirectional transmission of IAV between swine and humans commonly occurs. Once introduced into the swine population, human-origin IAV often reassorts with endemic swine IAV, resulting in reassortant viruses. Thus, it is imperative to develop a vaccine that is not only effective against IAV strains endemic in swine but also capable of preventing the spillover of human-origin IAV. In this study, we developed a lipid nanoparticle-encapsulated DNA plasmid vaccine (LNP-DNA) that demonstrates efficacy against both swine- and human-origin H1N1 viruses. The LNP-DNA vaccines are non-infectious and non-viable, meeting the criteria to serve as a vaccine platform for rapidly updating vaccines. Collectively, this LNP-DNA vaccine approach holds great potential for alleviating the impact of IAV on the swine industry and preventing the emergence of reassortant IAV strains.
2009 年,一种新型猪源 H1N1 病毒出现,引发了大流行。该病毒被称为 H1N1pdm09,迅速取代了流行的 H1 谱系,并成为感染人类的主要季节性甲型流感病毒亚型。H1N1pdm09 已频繁发生人-猪溢出,每次溢出都会导致猪群中持续传播人类来源的 H1N1pdm09。在本研究中,我们开发了一种基于脂质纳米颗粒的 DNA 疫苗(LNP-DNA),其中包含猪源 H1N1pdm09 的血凝素基因。在猪中,这种 LNP-DNA 疫苗在单次肌肉内免疫后可诱导出强大的抗体反应,并可保护猪免受同源猪源 H1N1pdm09 病毒的攻击感染。在小鼠模型中,LNP-DNA 疫苗可诱导抗体和 T 细胞反应,并可保护小鼠免受致死性攻击适应人类来源的 H1N1pdm09 病毒。这些发现表明,LNP-DNA 疫苗有可能预防猪源和人类来源的 H1N1pdm09 病毒。
甲型流感病毒(IAV)在猪中广泛传播,给养猪业造成重大经济损失。此外,IAV 在猪与人之间的双向传播很常见。一旦引入猪群,人类来源的 IAV 通常与地方性猪 IAV 重组,导致重组病毒。因此,开发一种不仅对猪地方性 IAV 株有效,而且能防止人类来源的 IAV 溢出的疫苗至关重要。在这项研究中,我们开发了一种脂质纳米颗粒包裹的 DNA 质粒疫苗(LNP-DNA),对猪源和人类来源的 H1N1 病毒均有效。LNP-DNA 疫苗是非传染性和非活性的,符合作为快速更新疫苗的疫苗平台的标准。总的来说,这种 LNP-DNA 疫苗方法具有很大的潜力,可以减轻 IAV 对养猪业的影响,并防止重组 IAV 株的出现。