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Cytokine modulation correlates with severity of monkeypox disease in humans

BACKGROUND: Human monkeypox is a zoonotic disease endemic to parts of Africa. Similar to other orthopoxviruses, virus and host have considerable interactions through immunomodulation. These interactions likely drive the establishment of a productive infection and disease progression, resulting in th...

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Autores principales: Johnston, Sara C., Johnson, Joshua C., Stonier, Spencer W., Lin, Kenny L., Kisalu, Neville K., Hensley, Lisa E., Rimoin, Anne W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. Published by Elsevier B.V. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533885/
https://www.ncbi.nlm.nih.gov/pubmed/25600603
http://dx.doi.org/10.1016/j.jcv.2014.12.001
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author Johnston, Sara C.
Johnson, Joshua C.
Stonier, Spencer W.
Lin, Kenny L.
Kisalu, Neville K.
Hensley, Lisa E.
Rimoin, Anne W.
author_facet Johnston, Sara C.
Johnson, Joshua C.
Stonier, Spencer W.
Lin, Kenny L.
Kisalu, Neville K.
Hensley, Lisa E.
Rimoin, Anne W.
author_sort Johnston, Sara C.
collection PubMed
description BACKGROUND: Human monkeypox is a zoonotic disease endemic to parts of Africa. Similar to other orthopoxviruses, virus and host have considerable interactions through immunomodulation. These interactions likely drive the establishment of a productive infection and disease progression, resulting in the range of disease presentations and case fatality rates observed for members of the Orthopoxvirus genus. OBJECTIVES: Much of our understanding about the immune response to orthopoxvirus infection comes from either in vitro or in vivo studies performed in small animals or non-human primates. Here, we conducted a detailed assessment of cytokine responses to monkeypox virus using serum from acutely ill humans collected during monkeypox active disease surveillance (2005–2007) in the Democratic Republic of the Congo. STUDY DESIGN: Nineteen serum samples that were from patients with confirmed monkeypox virus infections were selected for cytokine profiling. Cytokine profiling was performed on the Bio-Rad Bioplex 100 system using a 30-plex human cytokine panel. RESULTS: Cytokine profiling revealed elevated cytokine concentrations in all samples. Overproduction of certain cytokines (interleukin [IL]-2R, IL-10, and granulocyte macrophage-colony stimulating factor were observed in patients with serious disease (defined as >250 lesions based on the World Health Organization scoring system). CONCLUSIONS: The data suggest that cytokine modulation affects monkeypox disease severity in humans.
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spelling pubmed-95338852022-10-07 Cytokine modulation correlates with severity of monkeypox disease in humans Johnston, Sara C. Johnson, Joshua C. Stonier, Spencer W. Lin, Kenny L. Kisalu, Neville K. Hensley, Lisa E. Rimoin, Anne W. J Clin Virol Short Communication BACKGROUND: Human monkeypox is a zoonotic disease endemic to parts of Africa. Similar to other orthopoxviruses, virus and host have considerable interactions through immunomodulation. These interactions likely drive the establishment of a productive infection and disease progression, resulting in the range of disease presentations and case fatality rates observed for members of the Orthopoxvirus genus. OBJECTIVES: Much of our understanding about the immune response to orthopoxvirus infection comes from either in vitro or in vivo studies performed in small animals or non-human primates. Here, we conducted a detailed assessment of cytokine responses to monkeypox virus using serum from acutely ill humans collected during monkeypox active disease surveillance (2005–2007) in the Democratic Republic of the Congo. STUDY DESIGN: Nineteen serum samples that were from patients with confirmed monkeypox virus infections were selected for cytokine profiling. Cytokine profiling was performed on the Bio-Rad Bioplex 100 system using a 30-plex human cytokine panel. RESULTS: Cytokine profiling revealed elevated cytokine concentrations in all samples. Overproduction of certain cytokines (interleukin [IL]-2R, IL-10, and granulocyte macrophage-colony stimulating factor were observed in patients with serious disease (defined as >250 lesions based on the World Health Organization scoring system). CONCLUSIONS: The data suggest that cytokine modulation affects monkeypox disease severity in humans. Elsevier B.V. Published by Elsevier B.V. 2015-02 2014-12-04 /pmc/articles/PMC9533885/ /pubmed/25600603 http://dx.doi.org/10.1016/j.jcv.2014.12.001 Text en Copyright © 2014 Elsevier B.V. Published by Elsevier B.V. All rights reserved. Elsevier has created a Monkeypox Information Center in response to the declared public health emergency of international concern, with free information in English on the monkeypox virus. The Monkeypox Information Center is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its monkeypox related research that is available on the Monkeypox Information Center - including this research content - immediately available in publicly funded repositories, 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 Monkeypox Information Center remains active.
spellingShingle Short Communication
Johnston, Sara C.
Johnson, Joshua C.
Stonier, Spencer W.
Lin, Kenny L.
Kisalu, Neville K.
Hensley, Lisa E.
Rimoin, Anne W.
Cytokine modulation correlates with severity of monkeypox disease in humans
title Cytokine modulation correlates with severity of monkeypox disease in humans
title_full Cytokine modulation correlates with severity of monkeypox disease in humans
title_fullStr Cytokine modulation correlates with severity of monkeypox disease in humans
title_full_unstemmed Cytokine modulation correlates with severity of monkeypox disease in humans
title_short Cytokine modulation correlates with severity of monkeypox disease in humans
title_sort cytokine modulation correlates with severity of monkeypox disease in humans
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533885/
https://www.ncbi.nlm.nih.gov/pubmed/25600603
http://dx.doi.org/10.1016/j.jcv.2014.12.001
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