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Modulation of macrophage functions by sheeppox virus provides clues to understand interaction of the virus with host immune system

BACKGROUND: Poxviruses encode a range of immunomodulatory genes to subvert or evade the challenges posed by the innate and adaptive immune responses. However, the inactivated poxviruses possessed immunostimulating capacity and were used as a prophylactic or metaphylactic application that efficiently...

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Autores principales: Abu-EL-Saad, Abdel-Aziz S, Abdel-Moneim, Ahmed S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1079960/
https://www.ncbi.nlm.nih.gov/pubmed/15784144
http://dx.doi.org/10.1186/1743-422X-2-22
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author Abu-EL-Saad, Abdel-Aziz S
Abdel-Moneim, Ahmed S
author_facet Abu-EL-Saad, Abdel-Aziz S
Abdel-Moneim, Ahmed S
author_sort Abu-EL-Saad, Abdel-Aziz S
collection PubMed
description BACKGROUND: Poxviruses encode a range of immunomodulatory genes to subvert or evade the challenges posed by the innate and adaptive immune responses. However, the inactivated poxviruses possessed immunostimulating capacity and were used as a prophylactic or metaphylactic application that efficiently reduced susceptibility to infectious diseases in different species. This fact is intensively studied in different genera of poxviruses. However, little is known about the basic mechanisms adopted by sheeppox virus (SPPV). SPPV causes an acute disease of sheep that recently, has been observed to reinfect its host in spite of vaccination. RESULTS: By injecting inactivated or attenuated sheeppox virus SPPV vaccine in adult male Swiss mice, SPPV was found to reduce macrophages' functions in a local event that occurs at the site of application 12 h after vaccine administration as indicated by increased level of IL-10 and decreased level of SOD from cultured peritoneal macrophages. In contrast increased levels of IL-12, and SOD activity from cultured splenic macrophages, lymphocyte response to PHA-P, and in-vivo response to T-dependant Ag were detected. These effects were observed in both attenuated and inactivated SPPV, but more prominent in attenuated one. CONCLUSION: The results of this study help to elucidate, the phenomenon of existence natural SPPV infections in sheep instead of vaccination and the basic mechanisms responsible for the immunostimulating capacity of sheeppox virus. Locally, SPPV shows evidence for an immune escape mechanism that alleviates the host's immune response. Later and systemically, the virus protects the host from any fatal consequences of the immune system suppression.
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spelling pubmed-10799602005-04-15 Modulation of macrophage functions by sheeppox virus provides clues to understand interaction of the virus with host immune system Abu-EL-Saad, Abdel-Aziz S Abdel-Moneim, Ahmed S Virol J Research BACKGROUND: Poxviruses encode a range of immunomodulatory genes to subvert or evade the challenges posed by the innate and adaptive immune responses. However, the inactivated poxviruses possessed immunostimulating capacity and were used as a prophylactic or metaphylactic application that efficiently reduced susceptibility to infectious diseases in different species. This fact is intensively studied in different genera of poxviruses. However, little is known about the basic mechanisms adopted by sheeppox virus (SPPV). SPPV causes an acute disease of sheep that recently, has been observed to reinfect its host in spite of vaccination. RESULTS: By injecting inactivated or attenuated sheeppox virus SPPV vaccine in adult male Swiss mice, SPPV was found to reduce macrophages' functions in a local event that occurs at the site of application 12 h after vaccine administration as indicated by increased level of IL-10 and decreased level of SOD from cultured peritoneal macrophages. In contrast increased levels of IL-12, and SOD activity from cultured splenic macrophages, lymphocyte response to PHA-P, and in-vivo response to T-dependant Ag were detected. These effects were observed in both attenuated and inactivated SPPV, but more prominent in attenuated one. CONCLUSION: The results of this study help to elucidate, the phenomenon of existence natural SPPV infections in sheep instead of vaccination and the basic mechanisms responsible for the immunostimulating capacity of sheeppox virus. Locally, SPPV shows evidence for an immune escape mechanism that alleviates the host's immune response. Later and systemically, the virus protects the host from any fatal consequences of the immune system suppression. BioMed Central 2005-03-22 /pmc/articles/PMC1079960/ /pubmed/15784144 http://dx.doi.org/10.1186/1743-422X-2-22 Text en Copyright © 2005 Abu-EL-Saad and Abdel-Moneim; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Abu-EL-Saad, Abdel-Aziz S
Abdel-Moneim, Ahmed S
Modulation of macrophage functions by sheeppox virus provides clues to understand interaction of the virus with host immune system
title Modulation of macrophage functions by sheeppox virus provides clues to understand interaction of the virus with host immune system
title_full Modulation of macrophage functions by sheeppox virus provides clues to understand interaction of the virus with host immune system
title_fullStr Modulation of macrophage functions by sheeppox virus provides clues to understand interaction of the virus with host immune system
title_full_unstemmed Modulation of macrophage functions by sheeppox virus provides clues to understand interaction of the virus with host immune system
title_short Modulation of macrophage functions by sheeppox virus provides clues to understand interaction of the virus with host immune system
title_sort modulation of macrophage functions by sheeppox virus provides clues to understand interaction of the virus with host immune system
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1079960/
https://www.ncbi.nlm.nih.gov/pubmed/15784144
http://dx.doi.org/10.1186/1743-422X-2-22
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