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Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients

High levels of proinflammatory cytokines such as IFN-γ and TNF are associated with tissue lesions in cutaneous leishmaniasis (CL). We previously demonstrated that Schistosoma mansoni antigens downmodulate the in vitro cytokine response in CL. In the current study we evaluated whether S. mansoni anti...

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Autores principales: Bafica, Aline Michelle Barbosa, Cardoso, Luciana Santos, Oliveira, Sérgio Costa, Loukas, Alex, Góes, Alfredo, Oliveira, Ricardo Riccio, Carvalho, Edgar M., Araujo, Maria Ilma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504418/
https://www.ncbi.nlm.nih.gov/pubmed/23209879
http://dx.doi.org/10.1155/2012/520308
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author Bafica, Aline Michelle Barbosa
Cardoso, Luciana Santos
Oliveira, Sérgio Costa
Loukas, Alex
Góes, Alfredo
Oliveira, Ricardo Riccio
Carvalho, Edgar M.
Araujo, Maria Ilma
author_facet Bafica, Aline Michelle Barbosa
Cardoso, Luciana Santos
Oliveira, Sérgio Costa
Loukas, Alex
Góes, Alfredo
Oliveira, Ricardo Riccio
Carvalho, Edgar M.
Araujo, Maria Ilma
author_sort Bafica, Aline Michelle Barbosa
collection PubMed
description High levels of proinflammatory cytokines such as IFN-γ and TNF are associated with tissue lesions in cutaneous leishmaniasis (CL). We previously demonstrated that Schistosoma mansoni antigens downmodulate the in vitro cytokine response in CL. In the current study we evaluated whether S. mansoni antigens alter monocyte and T-lymphocyte phenotypes in leishmaniasis. Peripheral blood mononuclear cells of CL patients were cultured with L. braziliensis antigen in the presence or absence of the S. mansoni antigens rSm29, rSmTSP-2- and PIII. Cells were stained with fluorochrome conjugated antibodies and analyzed by flow cytometry. The addition of rSm29 to the cultures decreased the expression of HLA-DR in nonclassical (CD14(+)CD16(++)) monocytes, while the addition of PIII diminished the expression of this molecule in classical (CD14(++)CD16(−)) and intermediate (CD14(++)CD16(+)) monocytes. The addition of PIII and rSmTSP-2 resulted in downmodulation of CD80 expression in nonclassical and CD86 expression in intermediate monocytes, respectively. These two antigens increased the expression of CTLA-4 in CD4(+) T cells and they also expanded the frequency of CD4(+)CD25(high)Foxp3(+) T cells. Taken together, we show that S. mansoni antigens, mainly rSmTSP-2 and PIII, are able to decrease the activation status of monocytes and also to upregulate the expression of modulatory molecules in T lymphocytes.
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spelling pubmed-35044182012-12-03 Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients Bafica, Aline Michelle Barbosa Cardoso, Luciana Santos Oliveira, Sérgio Costa Loukas, Alex Góes, Alfredo Oliveira, Ricardo Riccio Carvalho, Edgar M. Araujo, Maria Ilma J Parasitol Res Clinical Study High levels of proinflammatory cytokines such as IFN-γ and TNF are associated with tissue lesions in cutaneous leishmaniasis (CL). We previously demonstrated that Schistosoma mansoni antigens downmodulate the in vitro cytokine response in CL. In the current study we evaluated whether S. mansoni antigens alter monocyte and T-lymphocyte phenotypes in leishmaniasis. Peripheral blood mononuclear cells of CL patients were cultured with L. braziliensis antigen in the presence or absence of the S. mansoni antigens rSm29, rSmTSP-2- and PIII. Cells were stained with fluorochrome conjugated antibodies and analyzed by flow cytometry. The addition of rSm29 to the cultures decreased the expression of HLA-DR in nonclassical (CD14(+)CD16(++)) monocytes, while the addition of PIII diminished the expression of this molecule in classical (CD14(++)CD16(−)) and intermediate (CD14(++)CD16(+)) monocytes. The addition of PIII and rSmTSP-2 resulted in downmodulation of CD80 expression in nonclassical and CD86 expression in intermediate monocytes, respectively. These two antigens increased the expression of CTLA-4 in CD4(+) T cells and they also expanded the frequency of CD4(+)CD25(high)Foxp3(+) T cells. Taken together, we show that S. mansoni antigens, mainly rSmTSP-2 and PIII, are able to decrease the activation status of monocytes and also to upregulate the expression of modulatory molecules in T lymphocytes. Hindawi Publishing Corporation 2012 2012-11-13 /pmc/articles/PMC3504418/ /pubmed/23209879 http://dx.doi.org/10.1155/2012/520308 Text en Copyright © 2012 Aline Michelle Barbosa Bafica et al. https://creativecommons.org/licenses/by/3.0/ 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 Clinical Study
Bafica, Aline Michelle Barbosa
Cardoso, Luciana Santos
Oliveira, Sérgio Costa
Loukas, Alex
Góes, Alfredo
Oliveira, Ricardo Riccio
Carvalho, Edgar M.
Araujo, Maria Ilma
Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients
title Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients
title_full Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients
title_fullStr Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients
title_full_unstemmed Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients
title_short Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients
title_sort changes in t-cell and monocyte phenotypes in vitro by schistosoma mansoni antigens in cutaneous leishmaniasis patients
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504418/
https://www.ncbi.nlm.nih.gov/pubmed/23209879
http://dx.doi.org/10.1155/2012/520308
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