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Safety and biodistribution of a double-deleted oncolytic vaccinia virus encoding CD40 ligand in laboratory Beagles

We evaluated adverse events, biodistribution and shedding of oncolytic vaccinia virus encoding CD40 ligand in two Beagles, in preparation for a phase 1 trial in canine cancer patients. Dog 1 received one dose of vaccinia virus and was euthanized 24 hours afterwards, while dog 2 received virus four t...

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Autores principales: Autio, Karoliina, Knuuttila, Anna, Kipar, Anja, Pesonen, Sari, Guse, Kilian, Parviainen, Suvi, Rajamäki, Minna, Laitinen-Vapaavuori, Outi, Vähä-Koskela, Markus, Kanerva, Anna, Hemminki, Akseli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782937/
https://www.ncbi.nlm.nih.gov/pubmed/27119092
http://dx.doi.org/10.1038/mto.2014.2
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author Autio, Karoliina
Knuuttila, Anna
Kipar, Anja
Pesonen, Sari
Guse, Kilian
Parviainen, Suvi
Rajamäki, Minna
Laitinen-Vapaavuori, Outi
Vähä-Koskela, Markus
Kanerva, Anna
Hemminki, Akseli
author_facet Autio, Karoliina
Knuuttila, Anna
Kipar, Anja
Pesonen, Sari
Guse, Kilian
Parviainen, Suvi
Rajamäki, Minna
Laitinen-Vapaavuori, Outi
Vähä-Koskela, Markus
Kanerva, Anna
Hemminki, Akseli
author_sort Autio, Karoliina
collection PubMed
description We evaluated adverse events, biodistribution and shedding of oncolytic vaccinia virus encoding CD40 ligand in two Beagles, in preparation for a phase 1 trial in canine cancer patients. Dog 1 received one dose of vaccinia virus and was euthanized 24 hours afterwards, while dog 2 received virus four times once weekly and was euthanized 7 days after that. Dogs were monitored for adverse events and underwent a detailed postmortem examination. Blood, saliva, urine, feces, and organs were collected for virus detection. Dog 1 had mild fever and lethargy while dog 2 experienced a possible seizure 5.5 hours after first virus administration. Viral DNA declined quickly in the blood after virus administration in both dogs but was still detectable 1 week later by quantitative polymerase chain reaction. Only samples taken directly after virus infusion contained infectious virus. Small amounts of viral DNA, but no infectious virus, were detected in a few saliva and urine samples. Necropsies did not reveal any relevant pathological changes and virus DNA was detected mainly in the spleen. The dogs in the study did not have cancer, and thus adverse events could be more common and viral load higher in dogs with tumors which allow viral amplification.
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spelling pubmed-47829372016-04-26 Safety and biodistribution of a double-deleted oncolytic vaccinia virus encoding CD40 ligand in laboratory Beagles Autio, Karoliina Knuuttila, Anna Kipar, Anja Pesonen, Sari Guse, Kilian Parviainen, Suvi Rajamäki, Minna Laitinen-Vapaavuori, Outi Vähä-Koskela, Markus Kanerva, Anna Hemminki, Akseli Mol Ther Oncolytics Article We evaluated adverse events, biodistribution and shedding of oncolytic vaccinia virus encoding CD40 ligand in two Beagles, in preparation for a phase 1 trial in canine cancer patients. Dog 1 received one dose of vaccinia virus and was euthanized 24 hours afterwards, while dog 2 received virus four times once weekly and was euthanized 7 days after that. Dogs were monitored for adverse events and underwent a detailed postmortem examination. Blood, saliva, urine, feces, and organs were collected for virus detection. Dog 1 had mild fever and lethargy while dog 2 experienced a possible seizure 5.5 hours after first virus administration. Viral DNA declined quickly in the blood after virus administration in both dogs but was still detectable 1 week later by quantitative polymerase chain reaction. Only samples taken directly after virus infusion contained infectious virus. Small amounts of viral DNA, but no infectious virus, were detected in a few saliva and urine samples. Necropsies did not reveal any relevant pathological changes and virus DNA was detected mainly in the spleen. The dogs in the study did not have cancer, and thus adverse events could be more common and viral load higher in dogs with tumors which allow viral amplification. Nature Publishing Group 2014-12-10 /pmc/articles/PMC4782937/ /pubmed/27119092 http://dx.doi.org/10.1038/mto.2014.2 Text en Copyright © 2014 American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Autio, Karoliina
Knuuttila, Anna
Kipar, Anja
Pesonen, Sari
Guse, Kilian
Parviainen, Suvi
Rajamäki, Minna
Laitinen-Vapaavuori, Outi
Vähä-Koskela, Markus
Kanerva, Anna
Hemminki, Akseli
Safety and biodistribution of a double-deleted oncolytic vaccinia virus encoding CD40 ligand in laboratory Beagles
title Safety and biodistribution of a double-deleted oncolytic vaccinia virus encoding CD40 ligand in laboratory Beagles
title_full Safety and biodistribution of a double-deleted oncolytic vaccinia virus encoding CD40 ligand in laboratory Beagles
title_fullStr Safety and biodistribution of a double-deleted oncolytic vaccinia virus encoding CD40 ligand in laboratory Beagles
title_full_unstemmed Safety and biodistribution of a double-deleted oncolytic vaccinia virus encoding CD40 ligand in laboratory Beagles
title_short Safety and biodistribution of a double-deleted oncolytic vaccinia virus encoding CD40 ligand in laboratory Beagles
title_sort safety and biodistribution of a double-deleted oncolytic vaccinia virus encoding cd40 ligand in laboratory beagles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782937/
https://www.ncbi.nlm.nih.gov/pubmed/27119092
http://dx.doi.org/10.1038/mto.2014.2
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