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Phenotypic characterisation of the cellular immune infiltrate in placentas of cattle following experimental inoculation with Neospora caninum in late gestation

Despite Neospora caninum being a major cause of bovine abortion worldwide, its pathogenesis is not completely understood. Neospora infection stimulates host cell-mediated immune responses, which may be responsible for the placental damage leading to abortion. The aim of the current study was to char...

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Autores principales: Cantón, Germán J, Katzer, Frank, Benavides-Silván, Julio, Maley, Stephen W, Palarea-Albaladejo, Javier, Pang, Yvonne, Smith, Sionagh, Bartley, Paul M, Rocchi, Mara, Innes, Elisabeth A, Chianini, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726360/
https://www.ncbi.nlm.nih.gov/pubmed/23876124
http://dx.doi.org/10.1186/1297-9716-44-60
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author Cantón, Germán J
Katzer, Frank
Benavides-Silván, Julio
Maley, Stephen W
Palarea-Albaladejo, Javier
Pang, Yvonne
Smith, Sionagh
Bartley, Paul M
Rocchi, Mara
Innes, Elisabeth A
Chianini, Francesca
author_facet Cantón, Germán J
Katzer, Frank
Benavides-Silván, Julio
Maley, Stephen W
Palarea-Albaladejo, Javier
Pang, Yvonne
Smith, Sionagh
Bartley, Paul M
Rocchi, Mara
Innes, Elisabeth A
Chianini, Francesca
author_sort Cantón, Germán J
collection PubMed
description Despite Neospora caninum being a major cause of bovine abortion worldwide, its pathogenesis is not completely understood. Neospora infection stimulates host cell-mediated immune responses, which may be responsible for the placental damage leading to abortion. The aim of the current study was to characterize the placental immune response following an experimental inoculation of pregnant cattle with N. caninum tachyzoites at day 210 of gestation. Cows were culled at 14, 28, 42 and 56 days post inoculation (dpi). Placentomes were examined by immunohistochemistry using antibodies against macrophages, T-cell subsets (CD4, CD8 and γδ), NK cells and B cells. Macrophages were detected mainly at 14 days post inoculation. Inflammation was generally mild and mainly characterized by CD3(+), CD4(+) and γδ T-cells; whereas CD8(+) and NK cells were less numerous. The immune cell repertoire observed in this study was similar to those seen in pregnant cattle challenged with N. caninum at early gestation. However, cellular infiltrates were less severe than those seen during first trimester Neospora infections. This may explain the milder clinical outcome observed when animals are infected late in gestation.
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spelling pubmed-37263602013-07-30 Phenotypic characterisation of the cellular immune infiltrate in placentas of cattle following experimental inoculation with Neospora caninum in late gestation Cantón, Germán J Katzer, Frank Benavides-Silván, Julio Maley, Stephen W Palarea-Albaladejo, Javier Pang, Yvonne Smith, Sionagh Bartley, Paul M Rocchi, Mara Innes, Elisabeth A Chianini, Francesca Vet Res Research Despite Neospora caninum being a major cause of bovine abortion worldwide, its pathogenesis is not completely understood. Neospora infection stimulates host cell-mediated immune responses, which may be responsible for the placental damage leading to abortion. The aim of the current study was to characterize the placental immune response following an experimental inoculation of pregnant cattle with N. caninum tachyzoites at day 210 of gestation. Cows were culled at 14, 28, 42 and 56 days post inoculation (dpi). Placentomes were examined by immunohistochemistry using antibodies against macrophages, T-cell subsets (CD4, CD8 and γδ), NK cells and B cells. Macrophages were detected mainly at 14 days post inoculation. Inflammation was generally mild and mainly characterized by CD3(+), CD4(+) and γδ T-cells; whereas CD8(+) and NK cells were less numerous. The immune cell repertoire observed in this study was similar to those seen in pregnant cattle challenged with N. caninum at early gestation. However, cellular infiltrates were less severe than those seen during first trimester Neospora infections. This may explain the milder clinical outcome observed when animals are infected late in gestation. BioMed Central 2013 2013-07-22 /pmc/articles/PMC3726360/ /pubmed/23876124 http://dx.doi.org/10.1186/1297-9716-44-60 Text en Copyright © 2013 Cantón et al.; 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
Cantón, Germán J
Katzer, Frank
Benavides-Silván, Julio
Maley, Stephen W
Palarea-Albaladejo, Javier
Pang, Yvonne
Smith, Sionagh
Bartley, Paul M
Rocchi, Mara
Innes, Elisabeth A
Chianini, Francesca
Phenotypic characterisation of the cellular immune infiltrate in placentas of cattle following experimental inoculation with Neospora caninum in late gestation
title Phenotypic characterisation of the cellular immune infiltrate in placentas of cattle following experimental inoculation with Neospora caninum in late gestation
title_full Phenotypic characterisation of the cellular immune infiltrate in placentas of cattle following experimental inoculation with Neospora caninum in late gestation
title_fullStr Phenotypic characterisation of the cellular immune infiltrate in placentas of cattle following experimental inoculation with Neospora caninum in late gestation
title_full_unstemmed Phenotypic characterisation of the cellular immune infiltrate in placentas of cattle following experimental inoculation with Neospora caninum in late gestation
title_short Phenotypic characterisation of the cellular immune infiltrate in placentas of cattle following experimental inoculation with Neospora caninum in late gestation
title_sort phenotypic characterisation of the cellular immune infiltrate in placentas of cattle following experimental inoculation with neospora caninum in late gestation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726360/
https://www.ncbi.nlm.nih.gov/pubmed/23876124
http://dx.doi.org/10.1186/1297-9716-44-60
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