Literature DB >> 33245745

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

Elene A Clemens1, Beth C Holbrook1, Masaru Kanekiyo2, Jonathan W Yewdell3, Barney S Graham2, Martha A Alexander-Miller1.   

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.
© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  HA stem; NHP; adjuvant; antibody; influenza vaccine; newborns; universal vaccine

Mesh:

Substances:

Year:  2021        PMID: 33245745      PMCID: PMC8280492          DOI: 10.1093/infdis/jiaa728

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  50 in total

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6.  Hemagglutinin head-specific responses dominate over stem-specific responses following prime boost with mismatched vaccines.

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Review 3.  Regulation and Function of Interferon-Lambda (IFNλ) and Its Receptor in Asthma.

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