tetano
Editor, Senior Moderator
Vet Microbiol
. 2025 Dec 21:313:110847.
doi: 10.1016/j.vetmic.2025.110847. Online ahead of print. Hemagglutinin-encoded mRNA vaccine confers efficient protection against H3N8 avian influenza virus in mice
Jiayan Wu[SUP] 1 [/SUP], Wenjie Jiang[SUP] 1 [/SUP], Xingyao Guo[SUP] 1 [/SUP], Jingwen Li[SUP] 1 [/SUP], Shengnan Wang[SUP] 1 [/SUP], Zhimin Wan[SUP] 1 [/SUP], Quan Xie[SUP] 1 [/SUP], Hongxia Shao[SUP] 1 [/SUP], Wei Gao[SUP] 1 [/SUP], Aijian Qin[SUP] 1 [/SUP], Tuofan Li[SUP] 2 [/SUP], Jianqiang Ye[SUP] 3 [/SUP]
Affiliations
Recently, the endemic of novel H3N8 avian influenza virus (AIV) in chickens poses significant threats to poultry industry and public health, driving the urgent need for safe and immunogenic vaccines. In this study, an mRNA vaccine, HA mRNA-LNP, expressing the hemagglutinin (HA) protein of H3N8 was developed. The sequence of HA of H3N8 was first codon-optimized and cloned into the pUC57 vector. The mRNA of the HA was synthesized by in vitro transcription (IVT) and enzymatic capping. The efficient expression of the HA protein of the mRNA was confirmed by Western blot, indirect immunofluorescence assay (IFA), and flow cytometry in 293 T or DF-1 cells. The mRNA vaccine was then encapsulated with lipid nanoparticle (LNP) named as HA mRNA-LNP. Furthermore, two doses of HA mRNA-LNP in mice through intramuscular vaccination elicited robust humoral immune response against H3N8, with peak hemagglutination inhibition (HI) and microneutralization (MN) titers reaching 1:5120 and 1:8192, respectively. This vaccine conferred efficient protection against the challenge of H3N8, evidenced by accelerated body weight recovery, undetectable viral loads in lung tissues, and milder pulmonary pathological changes. All these demonstrate that the HA mRNA-LNP vaccine generated here is a promising candidate for combating H3N8 infections.
Keywords: H3N8; HA; Protective efficacy; mRNA vaccine.
. 2025 Dec 21:313:110847.
doi: 10.1016/j.vetmic.2025.110847. Online ahead of print. Hemagglutinin-encoded mRNA vaccine confers efficient protection against H3N8 avian influenza virus in mice
Jiayan Wu[SUP] 1 [/SUP], Wenjie Jiang[SUP] 1 [/SUP], Xingyao Guo[SUP] 1 [/SUP], Jingwen Li[SUP] 1 [/SUP], Shengnan Wang[SUP] 1 [/SUP], Zhimin Wan[SUP] 1 [/SUP], Quan Xie[SUP] 1 [/SUP], Hongxia Shao[SUP] 1 [/SUP], Wei Gao[SUP] 1 [/SUP], Aijian Qin[SUP] 1 [/SUP], Tuofan Li[SUP] 2 [/SUP], Jianqiang Ye[SUP] 3 [/SUP]
Affiliations
- PMID: 41443052
- DOI: 10.1016/j.vetmic.2025.110847
Recently, the endemic of novel H3N8 avian influenza virus (AIV) in chickens poses significant threats to poultry industry and public health, driving the urgent need for safe and immunogenic vaccines. In this study, an mRNA vaccine, HA mRNA-LNP, expressing the hemagglutinin (HA) protein of H3N8 was developed. The sequence of HA of H3N8 was first codon-optimized and cloned into the pUC57 vector. The mRNA of the HA was synthesized by in vitro transcription (IVT) and enzymatic capping. The efficient expression of the HA protein of the mRNA was confirmed by Western blot, indirect immunofluorescence assay (IFA), and flow cytometry in 293 T or DF-1 cells. The mRNA vaccine was then encapsulated with lipid nanoparticle (LNP) named as HA mRNA-LNP. Furthermore, two doses of HA mRNA-LNP in mice through intramuscular vaccination elicited robust humoral immune response against H3N8, with peak hemagglutination inhibition (HI) and microneutralization (MN) titers reaching 1:5120 and 1:8192, respectively. This vaccine conferred efficient protection against the challenge of H3N8, evidenced by accelerated body weight recovery, undetectable viral loads in lung tissues, and milder pulmonary pathological changes. All these demonstrate that the HA mRNA-LNP vaccine generated here is a promising candidate for combating H3N8 infections.
Keywords: H3N8; HA; Protective efficacy; mRNA vaccine.