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An R848-Conjugated Influenza Virus Vaccine Elicits Robust Immunoglobulin G to Hemagglutinin Stem in a Newborn Nonhuman Primate Model

Elene A. Clemens, Beth C. Holbrook, Masaru Kanekiyo, Jonathan W. Yewdell, Barney S. Graham, Martha A. Alexander‐Miller

2020The Journal of Infectious Diseases18 citationsDOIOpen Access PDF

Abstract

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.

Topics & Concepts

VirologyHemagglutinin (influenza)BiologyVaccinationImmunologyVirusPopulationImmune systemAntibodyAdjuvantInfluenza vaccineInfluenza A virusTLR7EpitopeMedicineToll-like receptorInnate immune systemEnvironmental healthInfluenza Virus Research StudiesImmune Response and InflammationRespiratory viral infections research
An R848-Conjugated Influenza Virus Vaccine Elicits Robust Immunoglobulin G to Hemagglutinin Stem in a Newborn Nonhuman Primate Model | Litcius