Li Mingyang, Liu Mengyuan, Song Shaohui, Zhao Ruirui, Xie Yun, Liu Jing, Xu Lilan, Ma Xuefeng, Song Mingyu, Zhou Jian, Liao Guoyang
Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming 650118, China.
Vaccines (Basel). 2024 Mar 13;12(3):300. doi: 10.3390/vaccines12030300.
Vaccines are one of the most effective means of preventing influenza A, typically containing the hemagglutinin (HA) of the influenza A virus. However, antigenic drift and shift of the influenza A virus can lead to instability in vaccine efficacy. Compared to HA, the antigenic variation rate of neuraminidase (NA) is slower. In traditional inactivated influenza vaccines, although they contain a certain amount of NA, there are significant differences between different batches, which cannot consistently induce NA-based immune responses. Therefore, NA is often overlooked in vaccine development. In this study, we report an mRNA vaccine encoding the NA of two strains of influenza A virus. The experimental results demonstrated that when matched with the viral strain, this mRNA vaccine induced high levels of neutralizing antibodies, providing a protective effect to mice in viral challenge experiments, and this immune response was shown to be biased towards the Th1 type. In summary, this study demonstrates that NA is a promising potential antigen, providing new insights for the development of influenza A virus vaccines.
疫苗是预防甲型流感最有效的手段之一,通常含有甲型流感病毒的血凝素(HA)。然而,甲型流感病毒的抗原漂移和转变会导致疫苗效力不稳定。与HA相比,神经氨酸酶(NA)的抗原变异率较慢。在传统的灭活流感疫苗中,虽然含有一定量的NA,但不同批次之间存在显著差异,无法持续诱导基于NA的免疫反应。因此,NA在疫苗研发中常常被忽视。在本研究中,我们报道了一种编码两株甲型流感病毒NA的mRNA疫苗。实验结果表明,与病毒株匹配时,这种mRNA疫苗可诱导高水平的中和抗体,在病毒攻击实验中为小鼠提供保护作用,并且这种免疫反应显示偏向于Th1型。总之,本研究表明NA是一种有前景的潜在抗原,为甲型流感病毒疫苗的研发提供了新的见解。