AS03-Adjuvanted H5N1 Avian Influenza Vaccine Modulates Early Innate Immune Signatures in Human Peripheral Blood Mononuclear Cells.

Publication Type
Journal Article
Year of Publication
2019
Authors
Howard, Leigh M; Goll, Johannes B; Jensen, Travis L; Hoek, Kristen L; Prasad, Nripesh; Gelber, Casey E; Levy, Shawn E; Joyce, Sebastian; Link, Andrew J; Creech, C Buddy; Edwards, Kathryn M
Secondary
J Infect Dis
Volume
219
Pagination
1786-1798
Date Published
2019 05 05
Keywords
Adaptive Immunity; Adjuvants, Immunologic; Adult; alpha-Tocopherol; Double-Blind Method; Drug Combinations; Gene Expression Profiling; Humans; Immunity, Innate; Influenza A Virus, H5N1 Subtype; Influenza Vaccines; Influenza, Human; Leukocytes; Polysorbates; Signal Transduction; Squalene; Young Adult
Abstract

BACKGROUND: Adjuvant System 03 (AS03) markedly enhances responses to influenza A/H5N1 vaccines, but the mechanisms of this enhancement are incompletely understood.

METHODS: Using ribonucleic acid sequencing on peripheral blood mononuclear cells (PBMCs) from AS03-adjuvanted and unadjuvanted inactivated H5N1 vaccine recipients, we identified differentially expressed genes, enriched pathways, and genes that correlated with serologic responses. We compared bulk PBMC findings with our previously published assessments of flow-sorted immune cell types.

RESULTS: AS03-adjuvanted vaccine induced the strongest differential signals on day 1 postvaccination, activating multiple innate immune pathways including interferon and JAK-STAT signaling, Fcγ receptor (FcγR)-mediated phagocytosis, and antigen processing and presentation. Changes in signal transduction and immunoglobulin genes predicted peak hemagglutinin inhibition (HAI) titers. Compared with individual immune cell types, activated PBMC genes and pathways were most similar to innate immune cells. However, several pathways were unique to PBMCs, and several pathways identified in individual cell types were absent in PBMCs.

CONCLUSIONS: Transcriptomic analysis of PBMCs after AS03-adjuvanted H5N1 vaccination revealed early activation of innate immune signaling, including a 5- to 8-fold upregulation of FcγR1A/1B/1C genes. Several early gene responses were correlated with HAI titer, indicating links with the adaptive immune response. Although PBMCs and cell-specific results shared key innate immune signals, unique signals were identified by both approaches.