Department of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
J Infect Dis. 2021 Jul 15;224(2):351-359. doi: 10.1093/infdis/jiaa728.
Eliciting broadly protective antibodies is a critical goal for the development of more effective vaccines against influenza. Optimizing protection is of particular importance in newborns, who are highly vulnerable to severe disease following infection. An effective vaccination strategy for this population must surmount the challenges associated with the neonatal immune system as well as mitigate the inherent immune subdominance of conserved influenza virus epitopes, responses to which can provide broader protection. Here, we show that prime-boost vaccination with a TLR7/8 agonist (R848)-conjugated influenza A virus vaccine elicits antibody responses to the highly conserved hemagglutinin stem and promotes rapid induction of virus neutralizing stem-specific antibodies following viral challenge. These findings support the efficacy of R848 as an effective adjuvant for newborns and demonstrate its ability to enhance antibody responses to subdominant antigenic sites in this at-risk population.
诱导广泛保护性抗体是开发更有效的流感疫苗的关键目标。在新生儿中,优化保护尤其重要,因为他们在感染后极易患上重病。对于这一人群,有效的疫苗接种策略必须克服与新生儿免疫系统相关的挑战,并减轻保守流感病毒表位的固有免疫劣势,针对这些表位的反应可以提供更广泛的保护。在这里,我们表明,TLR7/8 激动剂(R848)缀合的流感 A 病毒疫苗的初免-加强免疫接种可诱导对高度保守的血凝素茎的抗体反应,并在病毒攻击后迅速诱导病毒中和茎特异性抗体。这些发现支持 R848 作为新生儿有效佐剂的功效,并证明其能够增强该高危人群中对次要抗原位点的抗体反应。