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Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
Adverse events upon smallpox vaccination with fully-replicative strains of Vaccinia virus (VACV) comprise an array of clinical manifestations that occur primarily in immunocompromised patients leading to significant host morbidity/mortality. The expansion of immune-suppressed populations and the pos...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078145/ https://www.ncbi.nlm.nih.gov/pubmed/21526210 http://dx.doi.org/10.1371/journal.pone.0018924 |
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author | Mota, Bruno E. F. Gallardo-Romero, Nadia Trindade, Giliane Keckler, M. Shannon Karem, Kevin Carroll, Darin Campos, Marco A. Vieira, Leda Q. da Fonseca, Flávio G. Ferreira, Paulo C. P. Bonjardim, Cláudio A. Damon, Inger K. Kroon, Erna G. |
author_facet | Mota, Bruno E. F. Gallardo-Romero, Nadia Trindade, Giliane Keckler, M. Shannon Karem, Kevin Carroll, Darin Campos, Marco A. Vieira, Leda Q. da Fonseca, Flávio G. Ferreira, Paulo C. P. Bonjardim, Cláudio A. Damon, Inger K. Kroon, Erna G. |
author_sort | Mota, Bruno E. F. |
collection | PubMed |
description | Adverse events upon smallpox vaccination with fully-replicative strains of Vaccinia virus (VACV) comprise an array of clinical manifestations that occur primarily in immunocompromised patients leading to significant host morbidity/mortality. The expansion of immune-suppressed populations and the possible release of Variola virus as a bioterrorist act have given rise to concerns over vaccination complications should more widespread vaccination be reinitiated. Our goal was to evaluate the components of the host immune system that are sufficient to prevent morbidity/mortality in a murine model of tail scarification, which mimics immunological and clinical features of smallpox vaccination in humans. Infection of C57BL/6 wild-type mice led to a strictly localized infection, with complete viral clearance by day 28 p.i. On the other hand, infection of T and B-cell deficient mice (Rag1 (−/−)) produced a severe disease, with uncontrolled viral replication at the inoculation site and dissemination to internal organs. Infection of B-cell deficient animals (µMT) produced no mortality. However, viral clearance in µMT animals was delayed compared to WT animals, with detectable viral titers in tail and internal organs late in infection. Treatment of Rag1 (−/−) with rabbit hyperimmune anti-vaccinia serum had a subtle effect on the morbidity/mortality of this strain, but it was effective in reduce viral titers in ovaries. Finally, NUDE athymic mice showed a similar outcome of infection as Rag1 (−/−), and passive transfer of WT T cells to Rag1 (−/−) animals proved fully effective in preventing morbidity/mortality. These results strongly suggest that both T and B cells are important in the immune response to primary VACV infection in mice, and that T-cells are required to control the infection at the inoculation site and providing help for B-cells to produce antibodies, which help to prevent viral dissemination. These insights might prove helpful to better identify individuals with higher risk of complications after infection with poxvirus. |
format | Text |
id | pubmed-3078145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30781452011-04-27 Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus Mota, Bruno E. F. Gallardo-Romero, Nadia Trindade, Giliane Keckler, M. Shannon Karem, Kevin Carroll, Darin Campos, Marco A. Vieira, Leda Q. da Fonseca, Flávio G. Ferreira, Paulo C. P. Bonjardim, Cláudio A. Damon, Inger K. Kroon, Erna G. PLoS One Research Article Adverse events upon smallpox vaccination with fully-replicative strains of Vaccinia virus (VACV) comprise an array of clinical manifestations that occur primarily in immunocompromised patients leading to significant host morbidity/mortality. The expansion of immune-suppressed populations and the possible release of Variola virus as a bioterrorist act have given rise to concerns over vaccination complications should more widespread vaccination be reinitiated. Our goal was to evaluate the components of the host immune system that are sufficient to prevent morbidity/mortality in a murine model of tail scarification, which mimics immunological and clinical features of smallpox vaccination in humans. Infection of C57BL/6 wild-type mice led to a strictly localized infection, with complete viral clearance by day 28 p.i. On the other hand, infection of T and B-cell deficient mice (Rag1 (−/−)) produced a severe disease, with uncontrolled viral replication at the inoculation site and dissemination to internal organs. Infection of B-cell deficient animals (µMT) produced no mortality. However, viral clearance in µMT animals was delayed compared to WT animals, with detectable viral titers in tail and internal organs late in infection. Treatment of Rag1 (−/−) with rabbit hyperimmune anti-vaccinia serum had a subtle effect on the morbidity/mortality of this strain, but it was effective in reduce viral titers in ovaries. Finally, NUDE athymic mice showed a similar outcome of infection as Rag1 (−/−), and passive transfer of WT T cells to Rag1 (−/−) animals proved fully effective in preventing morbidity/mortality. These results strongly suggest that both T and B cells are important in the immune response to primary VACV infection in mice, and that T-cells are required to control the infection at the inoculation site and providing help for B-cells to produce antibodies, which help to prevent viral dissemination. These insights might prove helpful to better identify individuals with higher risk of complications after infection with poxvirus. Public Library of Science 2011-04-15 /pmc/articles/PMC3078145/ /pubmed/21526210 http://dx.doi.org/10.1371/journal.pone.0018924 Text en 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 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Mota, Bruno E. F. Gallardo-Romero, Nadia Trindade, Giliane Keckler, M. Shannon Karem, Kevin Carroll, Darin Campos, Marco A. Vieira, Leda Q. da Fonseca, Flávio G. Ferreira, Paulo C. P. Bonjardim, Cláudio A. Damon, Inger K. Kroon, Erna G. Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus |
title | Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
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title_full | Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
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title_fullStr | Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
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title_full_unstemmed | Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
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title_short | Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
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title_sort | adverse events post smallpox-vaccination: insights from tail scarification infection in mice with vaccinia virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078145/ https://www.ncbi.nlm.nih.gov/pubmed/21526210 http://dx.doi.org/10.1371/journal.pone.0018924 |
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