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Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures

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 defect...

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Autores principales: Hazlewood, Jessamine E., Dumenil, Troy, Le, Thuy T., Slonchak, Andrii, Kazakoff, Stephen H., Patch, Ann-Marie, Gray, Lesley-Ann, Howley, Paul M., Liu, Liang, Hayball, John D., Yan, Kexin, Rawle, Daniel J., Prow, Natalie A., Suhrbier, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837487/
https://www.ncbi.nlm.nih.gov/pubmed/33439897
http://dx.doi.org/10.1371/journal.ppat.1009215
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author Hazlewood, Jessamine E.
Dumenil, Troy
Le, Thuy T.
Slonchak, Andrii
Kazakoff, Stephen H.
Patch, Ann-Marie
Gray, Lesley-Ann
Howley, Paul M.
Liu, Liang
Hayball, John D.
Yan, Kexin
Rawle, Daniel J.
Prow, Natalie A.
Suhrbier, Andreas
author_facet Hazlewood, Jessamine E.
Dumenil, Troy
Le, Thuy T.
Slonchak, Andrii
Kazakoff, Stephen H.
Patch, Ann-Marie
Gray, Lesley-Ann
Howley, Paul M.
Liu, Liang
Hayball, John D.
Yan, Kexin
Rawle, Daniel J.
Prow, Natalie A.
Suhrbier, Andreas
author_sort Hazlewood, Jessamine E.
collection PubMed
description 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.
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spelling pubmed-78374872021-02-02 Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures Hazlewood, Jessamine E. Dumenil, Troy Le, Thuy T. Slonchak, Andrii Kazakoff, Stephen H. Patch, Ann-Marie Gray, Lesley-Ann Howley, Paul M. Liu, Liang Hayball, John D. Yan, Kexin Rawle, Daniel J. Prow, Natalie A. Suhrbier, Andreas PLoS Pathog Research Article 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. Public Library of Science 2021-01-13 /pmc/articles/PMC7837487/ /pubmed/33439897 http://dx.doi.org/10.1371/journal.ppat.1009215 Text en © 2021 Hazlewood et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hazlewood, Jessamine E.
Dumenil, Troy
Le, Thuy T.
Slonchak, Andrii
Kazakoff, Stephen H.
Patch, Ann-Marie
Gray, Lesley-Ann
Howley, Paul M.
Liu, Liang
Hayball, John D.
Yan, Kexin
Rawle, Daniel J.
Prow, Natalie A.
Suhrbier, Andreas
Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures
title Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures
title_full Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures
title_fullStr Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures
title_full_unstemmed Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures
title_short Injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures
title_sort injection site vaccinology of a recombinant vaccinia-based vector reveals diverse innate immune signatures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837487/
https://www.ncbi.nlm.nih.gov/pubmed/33439897
http://dx.doi.org/10.1371/journal.ppat.1009215
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