Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Nat Commun. 2022 Aug 9;13(1):4677. doi: 10.1038/s41467-022-32149-8.
Messenger RNA (mRNA) vaccines represent a new, effective vaccine platform with high capacity for rapid development. Generation of a universal influenza virus vaccine with the potential to elicit long-lasting, broadly cross-reactive immune responses is a necessity for reducing influenza-associated morbidity and mortality. Here we focus on the development of a universal influenza B virus vaccine based on the lipid nanoparticle-encapsulated nucleoside-modified mRNA (mRNA-LNP) platform. We evaluate vaccine candidates based on different target antigens that afford protection against challenge with ancestral and recent influenza B viruses from both antigenic lineages. A pentavalent vaccine combining all tested antigens protects mice from morbidity at a very low dose of 50 ng per antigen after a single vaccination. These findings support the further advancement of nucleoside-modified mRNA-LNPs expressing multiple conserved antigens as universal influenza virus vaccine candidates.
信使 RNA(mRNA)疫苗代表了一种新的、有效的疫苗平台,具有快速开发的高能力。生成具有潜在能力引发持久、广泛交叉反应性免疫应答的通用流感病毒疫苗,是减少流感相关发病率和死亡率的必要条件。在这里,我们专注于基于脂质纳米颗粒包封的核苷修饰的 mRNA(mRNA-LNP)平台的通用流感 B 病毒疫苗的开发。我们根据不同的靶抗原评估候选疫苗,这些抗原提供针对来自两个抗原谱系的祖先和最近的流感 B 病毒的保护。一种五价疫苗结合了所有测试的抗原,在单次接种后,每个抗原仅需 50ng 的极低剂量即可保护小鼠免受发病。这些发现支持进一步推进表达多种保守抗原的核苷修饰的 mRNA-LNP 作为通用流感病毒疫苗候选物。