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Intranasal monkeypox marmoset model: Prophylactic antibody treatment provides benefit against severe monkeypox virus disease

Concerns regarding outbreaks of human monkeypox or the potential reintroduction of smallpox into an immunological naïve population have prompted the development of animal models and countermeasures. Here we present a marmoset model of monkeypox and smallpox disease utilizing a relevant poxvirus via...

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Autores principales: Mucker, Eric M., Wollen-Roberts, Suzanne E., Kimmel, Adrienne, Shamblin, Josh, Sampey, Darryl, Hooper, Jay W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029809/
https://www.ncbi.nlm.nih.gov/pubmed/29927927
http://dx.doi.org/10.1371/journal.pntd.0006581
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author Mucker, Eric M.
Wollen-Roberts, Suzanne E.
Kimmel, Adrienne
Shamblin, Josh
Sampey, Darryl
Hooper, Jay W.
author_facet Mucker, Eric M.
Wollen-Roberts, Suzanne E.
Kimmel, Adrienne
Shamblin, Josh
Sampey, Darryl
Hooper, Jay W.
author_sort Mucker, Eric M.
collection PubMed
description Concerns regarding outbreaks of human monkeypox or the potential reintroduction of smallpox into an immunological naïve population have prompted the development of animal models and countermeasures. Here we present a marmoset model of monkeypox and smallpox disease utilizing a relevant poxvirus via a natural exposure route. We found that 1000 plaque forming units (PFU) of Monkeypox virus was sufficient to recapitulate smallpox disease, to include an incubation period of approximately 13 days, followed by the onset of rash, and death between 15 and 17 days. Temporally accurate manifestation of viremia and oral shedding were also features. The number of lesions ranged from no lesions to 299, the most reported in a marmoset exposed to a poxvirus. To both evaluate the efficacy of our antibodies and the applicability of the model system, marmosets were prophylactically treated with two monoclonal antibodies, c7D11 and c8A. Of three marmosets, two were completely free of disease and a single marmoset died 8 days after the mock (n = 1) or PBS control(s) (n = 2). Evaluation of the serum levels of the three animals provided a possible explanation to the animal succumbing to disease. Interestingly, more females had lesions (and a greater number of lesions) and lower viral burden (viremia and oral shedding) than males in our studies, suggesting a possible gender effect.
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spelling pubmed-60298092018-07-19 Intranasal monkeypox marmoset model: Prophylactic antibody treatment provides benefit against severe monkeypox virus disease Mucker, Eric M. Wollen-Roberts, Suzanne E. Kimmel, Adrienne Shamblin, Josh Sampey, Darryl Hooper, Jay W. PLoS Negl Trop Dis Research Article Concerns regarding outbreaks of human monkeypox or the potential reintroduction of smallpox into an immunological naïve population have prompted the development of animal models and countermeasures. Here we present a marmoset model of monkeypox and smallpox disease utilizing a relevant poxvirus via a natural exposure route. We found that 1000 plaque forming units (PFU) of Monkeypox virus was sufficient to recapitulate smallpox disease, to include an incubation period of approximately 13 days, followed by the onset of rash, and death between 15 and 17 days. Temporally accurate manifestation of viremia and oral shedding were also features. The number of lesions ranged from no lesions to 299, the most reported in a marmoset exposed to a poxvirus. To both evaluate the efficacy of our antibodies and the applicability of the model system, marmosets were prophylactically treated with two monoclonal antibodies, c7D11 and c8A. Of three marmosets, two were completely free of disease and a single marmoset died 8 days after the mock (n = 1) or PBS control(s) (n = 2). Evaluation of the serum levels of the three animals provided a possible explanation to the animal succumbing to disease. Interestingly, more females had lesions (and a greater number of lesions) and lower viral burden (viremia and oral shedding) than males in our studies, suggesting a possible gender effect. Public Library of Science 2018-06-21 /pmc/articles/PMC6029809/ /pubmed/29927927 http://dx.doi.org/10.1371/journal.pntd.0006581 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Mucker, Eric M.
Wollen-Roberts, Suzanne E.
Kimmel, Adrienne
Shamblin, Josh
Sampey, Darryl
Hooper, Jay W.
Intranasal monkeypox marmoset model: Prophylactic antibody treatment provides benefit against severe monkeypox virus disease
title Intranasal monkeypox marmoset model: Prophylactic antibody treatment provides benefit against severe monkeypox virus disease
title_full Intranasal monkeypox marmoset model: Prophylactic antibody treatment provides benefit against severe monkeypox virus disease
title_fullStr Intranasal monkeypox marmoset model: Prophylactic antibody treatment provides benefit against severe monkeypox virus disease
title_full_unstemmed Intranasal monkeypox marmoset model: Prophylactic antibody treatment provides benefit against severe monkeypox virus disease
title_short Intranasal monkeypox marmoset model: Prophylactic antibody treatment provides benefit against severe monkeypox virus disease
title_sort intranasal monkeypox marmoset model: prophylactic antibody treatment provides benefit against severe monkeypox virus disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029809/
https://www.ncbi.nlm.nih.gov/pubmed/29927927
http://dx.doi.org/10.1371/journal.pntd.0006581
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