Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/130547
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Type: Journal article
Title: Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures
Author: Hazlewood, J.E.
Dumenil, T.
Le, T.T.
Slonchak, A.
Kazakoff, S.H.
Patch, A.M.
Gray, L.A.
Howley, P.M.
Liu, L.
Hayball, J.D.
Yan, K.
Rawle, D.J.
Prow, N.A.
Suhrbier, A.
Citation: PLoS Pathogens, 2021; 17(1):e1009215-1-e1009215-39
Publisher: Public Library of Science
Issue Date: 2021
ISSN: 1553-7366
1553-7374
Editor: McFadden, G.
Statement of
Responsibility: 
Jessamine E. Hazlewood, Troy Dumenil, Thuy T. Le, Andrii Slonchak, Stephen H. Kazakoff, Ann-Marie Patch ... et al.
Abstract: Poxvirus systems have been extensively used as vaccine vectors. Herein a RNA-Seq analysis of intramuscular injection sites provided detailed insights into host innate immune responses, as well as expression of vector and recombinant immunogen genes, after vaccination with a new multiplication defective, vaccinia-based vector, Sementis Copenhagen Vector. Chikungunya and Zika virus immunogen mRNA and protein expression was associated with necrosing skeletal muscle cells surrounded by mixed cellular infiltrates. The multiple adjuvant signatures at 12 hours post-vaccination were dominated by TLR3, 4 and 9, STING, MAVS, PKR and the inflammasome. Th1 cytokine signatures were dominated by IFNγ, TNF and IL1β, and chemokine signatures by CCL5 and CXCL12. Multiple signatures associated with dendritic cell stimulation were evident. By day seven, vaccine transcripts were absent, and cell death, neutrophil, macrophage and inflammation annotations had abated. No compelling arthritis signatures were identified. Such injection site vaccinology approaches should inform refinements in poxvirus-based vector design.
Keywords: Animals
Mice, Inbred C57BL
Mice
Vaccinia virus
Vaccinia
Vaccines, Synthetic
Vaccination
Genome, Viral
Genetic Vectors
Female
Immunity, Innate
Zika Virus
Zika Virus Infection
Injection Site Reaction
Vaccinology
RNA-Seq
Rights: © 2021 Hazlewood et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
DOI: 10.1371/journal.ppat.1009215
Grant ID: http://purl.org/au-research/grants/nhmrc/1141421
http://purl.org/au-research/grants/nhmrc/1173880
Published version: http://dx.doi.org/10.1371/journal.ppat.1009215
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