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Cytokine and Chemokine Profile in Individuals with Different Degrees of Periportal Fibrosis due to Schistosoma mansoni Infection
Periportal fibrosis in schistosomiasis has been associated to the host immune response to parasite antigens. We evaluated the immune response in S. mansoni infected individuals with different degrees of periportal fibrosis. Cytokine and chemokines were measured in serum and in supernatants of PBMC c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540765/ https://www.ncbi.nlm.nih.gov/pubmed/23320145 http://dx.doi.org/10.1155/2012/394981 |
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author | De Souza, Robson Da Paixão Cardoso, Luciana Santos Lopes, Giuseppe Tittoni Varela Almeida, Maria Cecília F. Oliveira, Ricardo Riccio Alcântara, Leda Maria Carvalho, Edgar M. Araujo, Maria Ilma |
author_facet | De Souza, Robson Da Paixão Cardoso, Luciana Santos Lopes, Giuseppe Tittoni Varela Almeida, Maria Cecília F. Oliveira, Ricardo Riccio Alcântara, Leda Maria Carvalho, Edgar M. Araujo, Maria Ilma |
author_sort | De Souza, Robson Da Paixão |
collection | PubMed |
description | Periportal fibrosis in schistosomiasis has been associated to the host immune response to parasite antigens. We evaluated the immune response in S. mansoni infected individuals with different degrees of periportal fibrosis. Cytokine and chemokines were measured in serum and in supernatants of PBMC cultures stimulated with the soluble adult worm (SWAP) or egg (SEA) antigens, using a sandwich ELISA. The levels of IL-5 in response to SEA were higher in individuals with moderate to severe fibrosis (310.9 pg/mL) compared to individuals without fibrosis (36.8 pg/mL; P = 0.0418). There was also a higher production of TNF-α in cultures stimulated with SWAP in patients with insipient fibrosis (1446 pg/mL) compared to those without fibrosis (756.1 pg/mL; P = 0.0319). The serum levels of IL-13 and MIP-1α were higher in subjects without fibrosis than in those with moderate to severe fibrosis. However a positive association between serum levels of IL-13, TNF-α, MIP-1α, and RANTES and S. mansoni parasite burden was found. From these data we conclude that IL-5 and TNF-α may participate in liver pathology in schistosomiasis. The positive association between IL-13, TNF-α, MIP-1α, and RANTES with parasite burden, however, might predict the development of liver pathology. |
format | Online Article Text |
id | pubmed-3540765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35407652013-01-14 Cytokine and Chemokine Profile in Individuals with Different Degrees of Periportal Fibrosis due to Schistosoma mansoni Infection De Souza, Robson Da Paixão Cardoso, Luciana Santos Lopes, Giuseppe Tittoni Varela Almeida, Maria Cecília F. Oliveira, Ricardo Riccio Alcântara, Leda Maria Carvalho, Edgar M. Araujo, Maria Ilma J Parasitol Res Research Article Periportal fibrosis in schistosomiasis has been associated to the host immune response to parasite antigens. We evaluated the immune response in S. mansoni infected individuals with different degrees of periportal fibrosis. Cytokine and chemokines were measured in serum and in supernatants of PBMC cultures stimulated with the soluble adult worm (SWAP) or egg (SEA) antigens, using a sandwich ELISA. The levels of IL-5 in response to SEA were higher in individuals with moderate to severe fibrosis (310.9 pg/mL) compared to individuals without fibrosis (36.8 pg/mL; P = 0.0418). There was also a higher production of TNF-α in cultures stimulated with SWAP in patients with insipient fibrosis (1446 pg/mL) compared to those without fibrosis (756.1 pg/mL; P = 0.0319). The serum levels of IL-13 and MIP-1α were higher in subjects without fibrosis than in those with moderate to severe fibrosis. However a positive association between serum levels of IL-13, TNF-α, MIP-1α, and RANTES and S. mansoni parasite burden was found. From these data we conclude that IL-5 and TNF-α may participate in liver pathology in schistosomiasis. The positive association between IL-13, TNF-α, MIP-1α, and RANTES with parasite burden, however, might predict the development of liver pathology. Hindawi Publishing Corporation 2012 2012-12-25 /pmc/articles/PMC3540765/ /pubmed/23320145 http://dx.doi.org/10.1155/2012/394981 Text en Copyright © 2012 Robson Da Paixão De Souza 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 | Research Article De Souza, Robson Da Paixão Cardoso, Luciana Santos Lopes, Giuseppe Tittoni Varela Almeida, Maria Cecília F. Oliveira, Ricardo Riccio Alcântara, Leda Maria Carvalho, Edgar M. Araujo, Maria Ilma Cytokine and Chemokine Profile in Individuals with Different Degrees of Periportal Fibrosis due to Schistosoma mansoni Infection |
title | Cytokine and Chemokine Profile in Individuals with Different Degrees of Periportal Fibrosis due to Schistosoma mansoni Infection |
title_full | Cytokine and Chemokine Profile in Individuals with Different Degrees of Periportal Fibrosis due to Schistosoma mansoni Infection |
title_fullStr | Cytokine and Chemokine Profile in Individuals with Different Degrees of Periportal Fibrosis due to Schistosoma mansoni Infection |
title_full_unstemmed | Cytokine and Chemokine Profile in Individuals with Different Degrees of Periportal Fibrosis due to Schistosoma mansoni Infection |
title_short | Cytokine and Chemokine Profile in Individuals with Different Degrees of Periportal Fibrosis due to Schistosoma mansoni Infection |
title_sort | cytokine and chemokine profile in individuals with different degrees of periportal fibrosis due to schistosoma mansoni infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540765/ https://www.ncbi.nlm.nih.gov/pubmed/23320145 http://dx.doi.org/10.1155/2012/394981 |
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