A combination influenza mRNA vaccine candidate provided broad protection against diverse influenza virus challenge

被引:0
|
作者
Tian, Yuying [1 ,3 ]
Deng, Zhuoya [1 ]
Chuai, Zhengran [2 ]
Li, Cong [1 ,3 ]
Chang, Liangzheng [1 ]
Sun, Fang [2 ]
Cao, Rui [1 ,3 ]
Yu, Hongyu [1 ,3 ]
Xiao, Ruixue [1 ,3 ]
Lu, Shuai [1 ]
Xu, Yan [1 ]
Yang, Penghui [1 ,3 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Inst Hepatobiliary Surg, Fac Hepatopancreato Biliary Surg, Med Ctr 1, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 5, Beijing 100039, Peoples R China
[3] Inner Mongolia Med Univ, Sch Basic Med, Hohhot, Peoples R China
基金
北京市自然科学基金;
关键词
mRNA vaccine; Influenza viruses; Influenza viruses mRNA vaccine; Immunoprotection; IMMUNOGENICITY;
D O I
10.1016/j.virol.2024.110125
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Influenza viruses present a significant threat to global health. The production of a universal vaccine is considered essential due to the ineffectiveness of current seasonal influenza vaccines against mutant strains. mRNA technology offers new prospects in vaccinology, with various candidates for different infectious diseases currently in development and testing phases. In this study, we encapsulated a universal influenza mRNA vaccine. The vaccine encoded influenza hemagglutinin (HA), nucleoprotein (NP), and three tandem repeats of matrix protein 2 (3M2e). Twice-vaccinated mice exhibited strong humoral and cell-mediated immune responses in vivo. Notably, these immune responses led to a significant reduction in viral load of the lungs in challenged mice, and also conferred protection against future wild-type H1N1, H3N2, or H5N1 influenza virus challenges. Our findings suggest that this mRNA-universal vaccine strategy for influenza virus may be instrumental in mitigating the impact of future influenza pandemics.
引用
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页数:10
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