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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/132355

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network_name_str CONICET Digital (CONICET)
spelling 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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