Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
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
_version_ 1782201923509682176
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
title_full Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
title_fullStr Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
title_full_unstemmed Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
title_short Adverse Events Post Smallpox-Vaccination: Insights from Tail Scarification Infection in Mice with Vaccinia virus
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
work_keys_str_mv AT motabrunoef adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT gallardoromeronadia adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT trindadegiliane adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT kecklermshannon adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT karemkevin adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT carrolldarin adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT camposmarcoa adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT vieiraledaq adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT dafonsecaflaviog adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT ferreirapaulocp adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT bonjardimclaudioa adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT damoningerk adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus
AT kroonernag adverseeventspostsmallpoxvaccinationinsightsfromtailscarificationinfectioninmicewithvacciniavirus