| Literature DB >> 34784508 |
David R McIlwain1, Han Chen2, Zainab Rahil2, Neda Hajiakhoond Bidoki3, Sizun Jiang4, Zach Bjornson2, Nikita S Kolhatkar5, C Josefina Martinez5, Brice Gaudillière6, Julien Hedou6, Nilanjan Mukherjee2, Christian M Schürch7, Angelica Trejo2, Melton Affrime8, Bonnie Bock8, Kenneth Kim9, David Liebowitz5, Nima Aghaeepour10, Sean N Tucker5, Garry P Nolan11.
Abstract
Developing new influenza vaccines with improved performance and easier administration routes hinges on defining correlates of protection. Vaccine-elicited cellular correlates of protection for influenza in humans have not yet been demonstrated. A phase-2 double-blind randomized placebo and active (inactivated influenza vaccine) controlled study provides evidence that a human-adenovirus-5-based oral influenza vaccine tablet (VXA-A1.1) can protect from H1N1 virus challenge in humans. Mass cytometry characterization of vaccine-elicited cellular immune responses identified shared and vaccine-type-specific responses across B and T cells. For VXA-A1.1, the abundance of hemagglutinin-specific plasmablasts and plasmablasts positive for integrin α4β7, phosphorylated STAT5, or lacking expression of CD62L at day 8 were significantly correlated with protection from developing viral shedding following virus challenge at day 90 and contributed to an effective machine learning model of protection. These findings reveal the characteristics of vaccine-elicited cellular correlates of protection for an oral influenza vaccine.Entities:
Keywords: CyTOF; cellular immunity; correlates of protection; influenza challenge study; influenza vaccine; mass cytometry
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Year: 2021 PMID: 34784508 PMCID: PMC8665113 DOI: 10.1016/j.chom.2021.10.009
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023