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Immune Response Induced by an Immunodominant 60 kDa Glycoprotein of the Cell Wall of Sporothrix schenckii in Two Mice Strains with Experimental Sporotrichosis

Cell wall (CW) components of fungus Sporothrix schenckii are the major inductors antigens of immune responses. The immunodominant 60 kDa glycoprotein (gp60) has been shown to be associated with the virulence of this fungus but its role in experimental sporotrichosis is unknown. In this work, the imm...

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Autores principales: Alba-Fierro, Carlos A., Pérez-Torres, Armando, Toriello, Conchita, Pulido-Camarillo, Evelyn, López-Romero, Everardo, Romo-Lozano, Yolanda, Gutiérrez-Sánchez, Gerardo, Ruiz-Baca, Estela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4808653/
https://www.ncbi.nlm.nih.gov/pubmed/27051673
http://dx.doi.org/10.1155/2016/6525831
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author Alba-Fierro, Carlos A.
Pérez-Torres, Armando
Toriello, Conchita
Pulido-Camarillo, Evelyn
López-Romero, Everardo
Romo-Lozano, Yolanda
Gutiérrez-Sánchez, Gerardo
Ruiz-Baca, Estela
author_facet Alba-Fierro, Carlos A.
Pérez-Torres, Armando
Toriello, Conchita
Pulido-Camarillo, Evelyn
López-Romero, Everardo
Romo-Lozano, Yolanda
Gutiérrez-Sánchez, Gerardo
Ruiz-Baca, Estela
author_sort Alba-Fierro, Carlos A.
collection PubMed
description Cell wall (CW) components of fungus Sporothrix schenckii are the major inductors antigens of immune responses. The immunodominant 60 kDa glycoprotein (gp60) has been shown to be associated with the virulence of this fungus but its role in experimental sporotrichosis is unknown. In this work, the immunological effects of CW-purified gp60 were investigated in a model of experimental subcutaneous sporotrichosis in normal and gp60-preimmunized C57BL/6 and BALB/c mice strains which were then infected with S. schenckii conidia. Results showed that both mice strains use different cytokine profiles in order to fight S. schenckii infection; C57BL/6 mice seem to use a Th17 response while BALB/c mice tend to depend on a Th1 profile. Preimmunization with gp60 showed a downregulatory effect on the immune response since cytokines levels were diminished in both strains. There were no significant differences in the magnitude of dorsoplantar inflammation between gp60-preimmunized and nonimmunized mice of both strains. However, skin lesions due to the infection in gp60-preimmunized mice were more severe in BALB/c than in C57BL/6 mice, suggesting that the antigen exerts a higher downregulatory effect on the Th1 response.
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spelling pubmed-48086532016-04-05 Immune Response Induced by an Immunodominant 60 kDa Glycoprotein of the Cell Wall of Sporothrix schenckii in Two Mice Strains with Experimental Sporotrichosis Alba-Fierro, Carlos A. Pérez-Torres, Armando Toriello, Conchita Pulido-Camarillo, Evelyn López-Romero, Everardo Romo-Lozano, Yolanda Gutiérrez-Sánchez, Gerardo Ruiz-Baca, Estela J Immunol Res Research Article Cell wall (CW) components of fungus Sporothrix schenckii are the major inductors antigens of immune responses. The immunodominant 60 kDa glycoprotein (gp60) has been shown to be associated with the virulence of this fungus but its role in experimental sporotrichosis is unknown. In this work, the immunological effects of CW-purified gp60 were investigated in a model of experimental subcutaneous sporotrichosis in normal and gp60-preimmunized C57BL/6 and BALB/c mice strains which were then infected with S. schenckii conidia. Results showed that both mice strains use different cytokine profiles in order to fight S. schenckii infection; C57BL/6 mice seem to use a Th17 response while BALB/c mice tend to depend on a Th1 profile. Preimmunization with gp60 showed a downregulatory effect on the immune response since cytokines levels were diminished in both strains. There were no significant differences in the magnitude of dorsoplantar inflammation between gp60-preimmunized and nonimmunized mice of both strains. However, skin lesions due to the infection in gp60-preimmunized mice were more severe in BALB/c than in C57BL/6 mice, suggesting that the antigen exerts a higher downregulatory effect on the Th1 response. Hindawi Publishing Corporation 2016 2016-03-14 /pmc/articles/PMC4808653/ /pubmed/27051673 http://dx.doi.org/10.1155/2016/6525831 Text en Copyright © 2016 Carlos A. Alba-Fierro et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Alba-Fierro, Carlos A.
Pérez-Torres, Armando
Toriello, Conchita
Pulido-Camarillo, Evelyn
López-Romero, Everardo
Romo-Lozano, Yolanda
Gutiérrez-Sánchez, Gerardo
Ruiz-Baca, Estela
Immune Response Induced by an Immunodominant 60 kDa Glycoprotein of the Cell Wall of Sporothrix schenckii in Two Mice Strains with Experimental Sporotrichosis
title Immune Response Induced by an Immunodominant 60 kDa Glycoprotein of the Cell Wall of Sporothrix schenckii in Two Mice Strains with Experimental Sporotrichosis
title_full Immune Response Induced by an Immunodominant 60 kDa Glycoprotein of the Cell Wall of Sporothrix schenckii in Two Mice Strains with Experimental Sporotrichosis
title_fullStr Immune Response Induced by an Immunodominant 60 kDa Glycoprotein of the Cell Wall of Sporothrix schenckii in Two Mice Strains with Experimental Sporotrichosis
title_full_unstemmed Immune Response Induced by an Immunodominant 60 kDa Glycoprotein of the Cell Wall of Sporothrix schenckii in Two Mice Strains with Experimental Sporotrichosis
title_short Immune Response Induced by an Immunodominant 60 kDa Glycoprotein of the Cell Wall of Sporothrix schenckii in Two Mice Strains with Experimental Sporotrichosis
title_sort immune response induced by an immunodominant 60 kda glycoprotein of the cell wall of sporothrix schenckii in two mice strains with experimental sporotrichosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4808653/
https://www.ncbi.nlm.nih.gov/pubmed/27051673
http://dx.doi.org/10.1155/2016/6525831
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