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Distribution and absence of generalized lesions in mice following single dose intramuscular inoculation of the vaccine candidate MVA-MERS-S
Modified Vaccinia Virus Ankara (MVA) is a highly attenuated and replication-deficient virus serving as vaccine against infectious diseases. Here, we assessed the in vivo distribution of a recombinant MVA candidate vaccine against the Middle Eastern Respiratory Syndrome (MVA-MERS-S) in mice. Intramus...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Alliance for Biological Standardization. Published by Elsevier Ltd.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128986/ https://www.ncbi.nlm.nih.gov/pubmed/29759890 http://dx.doi.org/10.1016/j.biologicals.2018.05.004 |
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author | Langenmayer, Martin C. Lülf-Averhoff, Anna-Theresa Adam-Neumair, Silvia Fux, Robert Sutter, Gerd Volz, Asisa |
author_facet | Langenmayer, Martin C. Lülf-Averhoff, Anna-Theresa Adam-Neumair, Silvia Fux, Robert Sutter, Gerd Volz, Asisa |
author_sort | Langenmayer, Martin C. |
collection | PubMed |
description | Modified Vaccinia Virus Ankara (MVA) is a highly attenuated and replication-deficient virus serving as vaccine against infectious diseases. Here, we assessed the in vivo distribution of a recombinant MVA candidate vaccine against the Middle Eastern Respiratory Syndrome (MVA-MERS-S) in mice. Intramuscularly inoculated mice were necropsied at different time points and examined by histology, immunohistochemistry and real-time PCR. We detected inflammation and myonecrosis at the parenteral site and hyperplasia of the draining lymph nodes. MVA-MERS-S did not result in detectable lesions in tissues peripheral to the parenteral site and draining lymph nodes. Real-time PCR analysis of >240 tissue samples detected MVA-DNA predominantly at the injection site and in the draining lymph nodes, and suggested continuous clearance of the candidate vaccine during the observation period. Levels of parenteral site inflammation and hyperplasia of draining lymph nodes were considered in line with immunological responses to vaccine inoculation. |
format | Online Article Text |
id | pubmed-7128986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | International Alliance for Biological Standardization. Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71289862020-04-08 Distribution and absence of generalized lesions in mice following single dose intramuscular inoculation of the vaccine candidate MVA-MERS-S Langenmayer, Martin C. Lülf-Averhoff, Anna-Theresa Adam-Neumair, Silvia Fux, Robert Sutter, Gerd Volz, Asisa Biologicals Article Modified Vaccinia Virus Ankara (MVA) is a highly attenuated and replication-deficient virus serving as vaccine against infectious diseases. Here, we assessed the in vivo distribution of a recombinant MVA candidate vaccine against the Middle Eastern Respiratory Syndrome (MVA-MERS-S) in mice. Intramuscularly inoculated mice were necropsied at different time points and examined by histology, immunohistochemistry and real-time PCR. We detected inflammation and myonecrosis at the parenteral site and hyperplasia of the draining lymph nodes. MVA-MERS-S did not result in detectable lesions in tissues peripheral to the parenteral site and draining lymph nodes. Real-time PCR analysis of >240 tissue samples detected MVA-DNA predominantly at the injection site and in the draining lymph nodes, and suggested continuous clearance of the candidate vaccine during the observation period. Levels of parenteral site inflammation and hyperplasia of draining lymph nodes were considered in line with immunological responses to vaccine inoculation. International Alliance for Biological Standardization. Published by Elsevier Ltd. 2018-07 2018-07-06 /pmc/articles/PMC7128986/ /pubmed/29759890 http://dx.doi.org/10.1016/j.biologicals.2018.05.004 Text en © 2018 International Alliance for Biological Standardization. Published by Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Langenmayer, Martin C. Lülf-Averhoff, Anna-Theresa Adam-Neumair, Silvia Fux, Robert Sutter, Gerd Volz, Asisa Distribution and absence of generalized lesions in mice following single dose intramuscular inoculation of the vaccine candidate MVA-MERS-S |
title | Distribution and absence of generalized lesions in mice following single dose intramuscular inoculation of the vaccine candidate MVA-MERS-S |
title_full | Distribution and absence of generalized lesions in mice following single dose intramuscular inoculation of the vaccine candidate MVA-MERS-S |
title_fullStr | Distribution and absence of generalized lesions in mice following single dose intramuscular inoculation of the vaccine candidate MVA-MERS-S |
title_full_unstemmed | Distribution and absence of generalized lesions in mice following single dose intramuscular inoculation of the vaccine candidate MVA-MERS-S |
title_short | Distribution and absence of generalized lesions in mice following single dose intramuscular inoculation of the vaccine candidate MVA-MERS-S |
title_sort | distribution and absence of generalized lesions in mice following single dose intramuscular inoculation of the vaccine candidate mva-mers-s |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128986/ https://www.ncbi.nlm.nih.gov/pubmed/29759890 http://dx.doi.org/10.1016/j.biologicals.2018.05.004 |
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