Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation
- Autores
- Mouriès, Juliette; Moron, Victor Gabriel; Schlecht, Géraldine; Escriou, Nicolas; Dadaglio, Gilles; Lederc, Claude
- Año de publicación
- 2008
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Cross-presentation is a crucial mechanism in tumoral and microbial immunity because it allows internalized cell associated or exogenous antigens (Ags) to be delivered into the major histocompatibility complex I pathway. This pathway is important for the development of CD8 + T-cell responses and for the induction of tolerance. In mice, cross-presentation is considered to be a unique property of CD8α + conventional dendritic cells (DCs). Here we show that splenic plasmacytoid DCs (pDCs) efficiently capture exogenous Ags in vivo but are not able to cross-present these Ags at steady state. However, in vitro and in vivo stimulation by Toll-like receptor-7, or -9 or viruses licenses pDCs to cross-present soluble or particulate Ags by a transporter associated with antigen processing-dependent mechanism. Induction of cross-presentation confers to pDCs the ability to generate efficient effectorCD8 + T-cell responses against exogenous Ags in vivo, showing that pDCs may play a crucial role in induction of adaptive immune responses against pathogens that do not infect tissues of hemopoietic origin. This study provides the first evidence for an in vivo role of splenic pDCs in Ag cross-presentation and T-cell crosspriming and suggests that pDCs may constitute an attractive target to boost the efficacy of vaccines based on cytotoxic T lymphocyte induction.
Fil: Mouriès, Juliette. Inserm; Francia. Institut Pasteur de Paris.; Francia
Fil: Moron, Victor Gabriel. Inserm; Francia. Institut Pasteur de Paris.; Francia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina
Fil: Schlecht, Géraldine. Inserm; Francia. Institut Pasteur de Paris.; Francia
Fil: Escriou, Nicolas. Inserm; Francia. Institut Pasteur de Paris.; Francia
Fil: Dadaglio, Gilles. Inserm; Francia. Institut Pasteur de Paris.; Francia
Fil: Lederc, Claude. Inserm; Francia. Institut Pasteur de Paris.; Francia - Materia
-
Plasmocitoid
Dendritic cells
Cross-presentation
Cytotoxicity - 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:11336/132355
Ver los metadatos del registro completo
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Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activationMouriès, JulietteMoron, Victor GabrielSchlecht, GéraldineEscriou, NicolasDadaglio, GillesLederc, ClaudePlasmocitoidDendritic cellsCross-presentationCytotoxicityhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Cross-presentation is a crucial mechanism in tumoral and microbial immunity because it allows internalized cell associated or exogenous antigens (Ags) to be delivered into the major histocompatibility complex I pathway. This pathway is important for the development of CD8 + T-cell responses and for the induction of tolerance. In mice, cross-presentation is considered to be a unique property of CD8α + conventional dendritic cells (DCs). Here we show that splenic plasmacytoid DCs (pDCs) efficiently capture exogenous Ags in vivo but are not able to cross-present these Ags at steady state. However, in vitro and in vivo stimulation by Toll-like receptor-7, or -9 or viruses licenses pDCs to cross-present soluble or particulate Ags by a transporter associated with antigen processing-dependent mechanism. Induction of cross-presentation confers to pDCs the ability to generate efficient effectorCD8 + T-cell responses against exogenous Ags in vivo, showing that pDCs may play a crucial role in induction of adaptive immune responses against pathogens that do not infect tissues of hemopoietic origin. This study provides the first evidence for an in vivo role of splenic pDCs in Ag cross-presentation and T-cell crosspriming and suggests that pDCs may constitute an attractive target to boost the efficacy of vaccines based on cytotoxic T lymphocyte induction.Fil: Mouriès, Juliette. Inserm; Francia. Institut Pasteur de Paris.; FranciaFil: Moron, Victor Gabriel. Inserm; Francia. Institut Pasteur de Paris.; Francia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; ArgentinaFil: Schlecht, Géraldine. Inserm; Francia. Institut Pasteur de Paris.; FranciaFil: Escriou, Nicolas. Inserm; Francia. Institut Pasteur de Paris.; FranciaFil: Dadaglio, Gilles. Inserm; Francia. Institut Pasteur de Paris.; FranciaFil: Lederc, Claude. Inserm; Francia. Institut Pasteur de Paris.; FranciaAmerican Society of Hematology2008-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/132355Mouriès, Juliette; Moron, Victor Gabriel; Schlecht, Géraldine; Escriou, Nicolas; Dadaglio, Gilles; et al.; Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation; American Society of Hematology; Blood; 112; 9; 11-2008; 3713-37220006-49711528-0020CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1182/blood-2008-03-146290info:eu-repo/semantics/altIdentifier/url/https://ashpublications.org/blood/article/112/9/3713/125900/Plasmacytoid-dendritic-cells-efficiently-crossinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:59:36Zoai:ri.conicet.gov.ar:11336/132355instacron: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:34982025-09-03 09:59:36.319CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation |
title |
Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation |
spellingShingle |
Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation Mouriès, Juliette Plasmocitoid Dendritic cells Cross-presentation Cytotoxicity |
title_short |
Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation |
title_full |
Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation |
title_fullStr |
Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation |
title_full_unstemmed |
Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation |
title_sort |
Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation |
dc.creator.none.fl_str_mv |
Mouriès, Juliette Moron, Victor Gabriel Schlecht, Géraldine Escriou, Nicolas Dadaglio, Gilles Lederc, Claude |
author |
Mouriès, Juliette |
author_facet |
Mouriès, Juliette Moron, Victor Gabriel Schlecht, Géraldine Escriou, Nicolas Dadaglio, Gilles Lederc, Claude |
author_role |
author |
author2 |
Moron, Victor Gabriel Schlecht, Géraldine Escriou, Nicolas Dadaglio, Gilles Lederc, Claude |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Plasmocitoid Dendritic cells Cross-presentation Cytotoxicity |
topic |
Plasmocitoid Dendritic cells Cross-presentation Cytotoxicity |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Cross-presentation is a crucial mechanism in tumoral and microbial immunity because it allows internalized cell associated or exogenous antigens (Ags) to be delivered into the major histocompatibility complex I pathway. This pathway is important for the development of CD8 + T-cell responses and for the induction of tolerance. In mice, cross-presentation is considered to be a unique property of CD8α + conventional dendritic cells (DCs). Here we show that splenic plasmacytoid DCs (pDCs) efficiently capture exogenous Ags in vivo but are not able to cross-present these Ags at steady state. However, in vitro and in vivo stimulation by Toll-like receptor-7, or -9 or viruses licenses pDCs to cross-present soluble or particulate Ags by a transporter associated with antigen processing-dependent mechanism. Induction of cross-presentation confers to pDCs the ability to generate efficient effectorCD8 + T-cell responses against exogenous Ags in vivo, showing that pDCs may play a crucial role in induction of adaptive immune responses against pathogens that do not infect tissues of hemopoietic origin. This study provides the first evidence for an in vivo role of splenic pDCs in Ag cross-presentation and T-cell crosspriming and suggests that pDCs may constitute an attractive target to boost the efficacy of vaccines based on cytotoxic T lymphocyte induction. Fil: Mouriès, Juliette. Inserm; Francia. Institut Pasteur de Paris.; Francia Fil: Moron, Victor Gabriel. Inserm; Francia. Institut Pasteur de Paris.; Francia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina Fil: Schlecht, Géraldine. Inserm; Francia. Institut Pasteur de Paris.; Francia Fil: Escriou, Nicolas. Inserm; Francia. Institut Pasteur de Paris.; Francia Fil: Dadaglio, Gilles. Inserm; Francia. Institut Pasteur de Paris.; Francia Fil: Lederc, Claude. Inserm; Francia. Institut Pasteur de Paris.; Francia |
description |
Cross-presentation is a crucial mechanism in tumoral and microbial immunity because it allows internalized cell associated or exogenous antigens (Ags) to be delivered into the major histocompatibility complex I pathway. This pathway is important for the development of CD8 + T-cell responses and for the induction of tolerance. In mice, cross-presentation is considered to be a unique property of CD8α + conventional dendritic cells (DCs). Here we show that splenic plasmacytoid DCs (pDCs) efficiently capture exogenous Ags in vivo but are not able to cross-present these Ags at steady state. However, in vitro and in vivo stimulation by Toll-like receptor-7, or -9 or viruses licenses pDCs to cross-present soluble or particulate Ags by a transporter associated with antigen processing-dependent mechanism. Induction of cross-presentation confers to pDCs the ability to generate efficient effectorCD8 + T-cell responses against exogenous Ags in vivo, showing that pDCs may play a crucial role in induction of adaptive immune responses against pathogens that do not infect tissues of hemopoietic origin. This study provides the first evidence for an in vivo role of splenic pDCs in Ag cross-presentation and T-cell crosspriming and suggests that pDCs may constitute an attractive target to boost the efficacy of vaccines based on cytotoxic T lymphocyte induction. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-11 |
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/11336/132355 Mouriès, Juliette; Moron, Victor Gabriel; Schlecht, Géraldine; Escriou, Nicolas; Dadaglio, Gilles; et al.; Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation; American Society of Hematology; Blood; 112; 9; 11-2008; 3713-3722 0006-4971 1528-0020 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/132355 |
identifier_str_mv |
Mouriès, Juliette; Moron, Victor Gabriel; Schlecht, Géraldine; Escriou, Nicolas; Dadaglio, Gilles; et al.; Plasmacytoid dendritic cells efficiently cross-prime naive T cells in vivo after TLR activation; American Society of Hematology; Blood; 112; 9; 11-2008; 3713-3722 0006-4971 1528-0020 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1182/blood-2008-03-146290 info:eu-repo/semantics/altIdentifier/url/https://ashpublications.org/blood/article/112/9/3713/125900/Plasmacytoid-dendritic-cells-efficiently-cross |
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 |
American Society of Hematology |
publisher.none.fl_str_mv |
American Society of Hematology |
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) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
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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1842269589991325696 |
score |
13.13397 |