Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells
- Autores
- Rodriguez, Ernesto; Noya, Verónica; Cervi, Laura Alejandra; Chiribao, Maria Laura; Brossard, Natalie; Chiale, Carolina; Carmona, Carlos; Giacomini, Cecilia; Freire, Teresa
- Año de publicación
- 2015
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Helminths express various carbohydrate-containing glycoconjugates on their surface, and they release glycan-rich excretion/secretion products that can be very important in their life cycles, infection and pathology. Recent evidence suggests that parasite glycoconjugates could play a role in the evasion of the immune response, leading to a modified Th2-polarized immune response that favors parasite survival in the host. Nevertheless, there is limited information about the nature or function of glycans produced by the trematode Fasciola hepatica, the causative agent of fasciolosis. In this paper, we investigate whether glycosylated molecules from F. hepatica participate in the modulation of host immunity. We also focus on dendritic cells, since they are an important target of immune-modulation by helminths, affecting their activity or function. Our results indicate that glycans from F. hepatica promote the production of IL-4 and IL-10, suppressing IFNγ production. During infection, this parasite is able to induce a semi-mature phenotype of DCs expressing low levels of MHCII and secrete IL-10. Furthermore, we show that parasite glycoconjugates mediate the modulation of LPS-induced maturation of DCs since their oxidation restores the capacity of LPS-treated DCs to secrete high levels of the pro-inflammatory cytokines IL-6 and IL-12/23p40 and low levels of the anti-inflammatory cytokine IL-10. Inhibition assays using carbohydrates suggest that the immune-modulation is mediated, at least in part, by the recognition of a mannose specific-CLR that signals by recruiting the phosphatase Php2. The results presented here contribute to the understanding of the role of parasite glycosylated molecules in the modulation of the host immunity and might be useful in the design of vaccines against fasciolosis.
Fil: Rodriguez, Ernesto. Universidad de la República; Uruguay
Fil: Noya, Verónica. Universidad de la República; Uruguay
Fil: Cervi, Laura Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina
Fil: Chiribao, Maria Laura. Universidad de la República; Uruguay
Fil: Brossard, Natalie. Universidad de la República; Uruguay
Fil: Chiale, Carolina. Universidad de la República; Uruguay
Fil: Carmona, Carlos. Universidad de la República; Uruguay
Fil: Giacomini, Cecilia. Universidad de la República; Uruguay
Fil: Freire, Teresa. Universidad de la República; Uruguay - Materia
-
FASCIOLA HEPATICA
GLYCANS
DENDRITIC CELLS
TLR: MATURATION - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/46078
Ver los metadatos del registro completo
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spelling |
Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cellsRodriguez, ErnestoNoya, VerónicaCervi, Laura AlejandraChiribao, Maria LauraBrossard, NatalieChiale, CarolinaCarmona, CarlosGiacomini, CeciliaFreire, TeresaFASCIOLA HEPATICAGLYCANSDENDRITIC CELLSTLR: MATURATIONhttps://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3Helminths express various carbohydrate-containing glycoconjugates on their surface, and they release glycan-rich excretion/secretion products that can be very important in their life cycles, infection and pathology. Recent evidence suggests that parasite glycoconjugates could play a role in the evasion of the immune response, leading to a modified Th2-polarized immune response that favors parasite survival in the host. Nevertheless, there is limited information about the nature or function of glycans produced by the trematode Fasciola hepatica, the causative agent of fasciolosis. In this paper, we investigate whether glycosylated molecules from F. hepatica participate in the modulation of host immunity. We also focus on dendritic cells, since they are an important target of immune-modulation by helminths, affecting their activity or function. Our results indicate that glycans from F. hepatica promote the production of IL-4 and IL-10, suppressing IFNγ production. During infection, this parasite is able to induce a semi-mature phenotype of DCs expressing low levels of MHCII and secrete IL-10. Furthermore, we show that parasite glycoconjugates mediate the modulation of LPS-induced maturation of DCs since their oxidation restores the capacity of LPS-treated DCs to secrete high levels of the pro-inflammatory cytokines IL-6 and IL-12/23p40 and low levels of the anti-inflammatory cytokine IL-10. Inhibition assays using carbohydrates suggest that the immune-modulation is mediated, at least in part, by the recognition of a mannose specific-CLR that signals by recruiting the phosphatase Php2. The results presented here contribute to the understanding of the role of parasite glycosylated molecules in the modulation of the host immunity and might be useful in the design of vaccines against fasciolosis.Fil: Rodriguez, Ernesto. Universidad de la República; UruguayFil: Noya, Verónica. Universidad de la República; UruguayFil: Cervi, Laura Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; ArgentinaFil: Chiribao, Maria Laura. Universidad de la República; UruguayFil: Brossard, Natalie. Universidad de la República; UruguayFil: Chiale, Carolina. Universidad de la República; UruguayFil: Carmona, Carlos. Universidad de la República; UruguayFil: Giacomini, Cecilia. Universidad de la República; UruguayFil: Freire, Teresa. Universidad de la República; UruguayPublic Library of Science2015-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/46078Rodriguez, Ernesto; Noya, Verónica; Cervi, Laura Alejandra; Chiribao, Maria Laura; Brossard, Natalie; et al.; Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells; Public Library of Science; Neglected Tropical Diseases; 31; 12; 12-2015; 1-261935-27271935-2735CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pntd.0004234info:eu-repo/semantics/altIdentifier/url/http://journals.plos.org/plosntds/article?id=10.1371/journal.pntd.0004234info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:05:13Zoai:ri.conicet.gov.ar:11336/46078instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-10 13:05:13.849CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells |
title |
Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells |
spellingShingle |
Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells Rodriguez, Ernesto FASCIOLA HEPATICA GLYCANS DENDRITIC CELLS TLR: MATURATION |
title_short |
Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells |
title_full |
Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells |
title_fullStr |
Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells |
title_full_unstemmed |
Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells |
title_sort |
Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells |
dc.creator.none.fl_str_mv |
Rodriguez, Ernesto Noya, Verónica Cervi, Laura Alejandra Chiribao, Maria Laura Brossard, Natalie Chiale, Carolina Carmona, Carlos Giacomini, Cecilia Freire, Teresa |
author |
Rodriguez, Ernesto |
author_facet |
Rodriguez, Ernesto Noya, Verónica Cervi, Laura Alejandra Chiribao, Maria Laura Brossard, Natalie Chiale, Carolina Carmona, Carlos Giacomini, Cecilia Freire, Teresa |
author_role |
author |
author2 |
Noya, Verónica Cervi, Laura Alejandra Chiribao, Maria Laura Brossard, Natalie Chiale, Carolina Carmona, Carlos Giacomini, Cecilia Freire, Teresa |
author2_role |
author author author author author author author author |
dc.subject.none.fl_str_mv |
FASCIOLA HEPATICA GLYCANS DENDRITIC CELLS TLR: MATURATION |
topic |
FASCIOLA HEPATICA GLYCANS DENDRITIC CELLS TLR: MATURATION |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.3 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Helminths express various carbohydrate-containing glycoconjugates on their surface, and they release glycan-rich excretion/secretion products that can be very important in their life cycles, infection and pathology. Recent evidence suggests that parasite glycoconjugates could play a role in the evasion of the immune response, leading to a modified Th2-polarized immune response that favors parasite survival in the host. Nevertheless, there is limited information about the nature or function of glycans produced by the trematode Fasciola hepatica, the causative agent of fasciolosis. In this paper, we investigate whether glycosylated molecules from F. hepatica participate in the modulation of host immunity. We also focus on dendritic cells, since they are an important target of immune-modulation by helminths, affecting their activity or function. Our results indicate that glycans from F. hepatica promote the production of IL-4 and IL-10, suppressing IFNγ production. During infection, this parasite is able to induce a semi-mature phenotype of DCs expressing low levels of MHCII and secrete IL-10. Furthermore, we show that parasite glycoconjugates mediate the modulation of LPS-induced maturation of DCs since their oxidation restores the capacity of LPS-treated DCs to secrete high levels of the pro-inflammatory cytokines IL-6 and IL-12/23p40 and low levels of the anti-inflammatory cytokine IL-10. Inhibition assays using carbohydrates suggest that the immune-modulation is mediated, at least in part, by the recognition of a mannose specific-CLR that signals by recruiting the phosphatase Php2. The results presented here contribute to the understanding of the role of parasite glycosylated molecules in the modulation of the host immunity and might be useful in the design of vaccines against fasciolosis. Fil: Rodriguez, Ernesto. Universidad de la República; Uruguay Fil: Noya, Verónica. Universidad de la República; Uruguay Fil: Cervi, Laura Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina Fil: Chiribao, Maria Laura. Universidad de la República; Uruguay Fil: Brossard, Natalie. Universidad de la República; Uruguay Fil: Chiale, Carolina. Universidad de la República; Uruguay Fil: Carmona, Carlos. Universidad de la República; Uruguay Fil: Giacomini, Cecilia. Universidad de la República; Uruguay Fil: Freire, Teresa. Universidad de la República; Uruguay |
description |
Helminths express various carbohydrate-containing glycoconjugates on their surface, and they release glycan-rich excretion/secretion products that can be very important in their life cycles, infection and pathology. Recent evidence suggests that parasite glycoconjugates could play a role in the evasion of the immune response, leading to a modified Th2-polarized immune response that favors parasite survival in the host. Nevertheless, there is limited information about the nature or function of glycans produced by the trematode Fasciola hepatica, the causative agent of fasciolosis. In this paper, we investigate whether glycosylated molecules from F. hepatica participate in the modulation of host immunity. We also focus on dendritic cells, since they are an important target of immune-modulation by helminths, affecting their activity or function. Our results indicate that glycans from F. hepatica promote the production of IL-4 and IL-10, suppressing IFNγ production. During infection, this parasite is able to induce a semi-mature phenotype of DCs expressing low levels of MHCII and secrete IL-10. Furthermore, we show that parasite glycoconjugates mediate the modulation of LPS-induced maturation of DCs since their oxidation restores the capacity of LPS-treated DCs to secrete high levels of the pro-inflammatory cytokines IL-6 and IL-12/23p40 and low levels of the anti-inflammatory cytokine IL-10. Inhibition assays using carbohydrates suggest that the immune-modulation is mediated, at least in part, by the recognition of a mannose specific-CLR that signals by recruiting the phosphatase Php2. The results presented here contribute to the understanding of the role of parasite glycosylated molecules in the modulation of the host immunity and might be useful in the design of vaccines against fasciolosis. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-12 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/46078 Rodriguez, Ernesto; Noya, Verónica; Cervi, Laura Alejandra; Chiribao, Maria Laura; Brossard, Natalie; et al.; Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells; Public Library of Science; Neglected Tropical Diseases; 31; 12; 12-2015; 1-26 1935-2727 1935-2735 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/46078 |
identifier_str_mv |
Rodriguez, Ernesto; Noya, Verónica; Cervi, Laura Alejandra; Chiribao, Maria Laura; Brossard, Natalie; et al.; Glycans from Fasciola hepatica modulate the host immune response and TLR-Induced maturation of dendritic cells; Public Library of Science; Neglected Tropical Diseases; 31; 12; 12-2015; 1-26 1935-2727 1935-2735 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pntd.0004234 info:eu-repo/semantics/altIdentifier/url/http://journals.plos.org/plosntds/article?id=10.1371/journal.pntd.0004234 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Public Library of Science |
publisher.none.fl_str_mv |
Public Library of Science |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842980186409140224 |
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12.993085 |