Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus
- Autores
- Mackern Oberti, Juan Pablo; Llanos, Carolina; Riedel, Claudia A.; Bueno, Susan M.; Kalergis, Alexis M.
- Año de publicación
- 2015
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Systemic lupus erythematosus (SLE) is a heterogeneous disease in which excessive inflammation, autoantibodies and complement activation lead to multisystem tissue damage. The contribution of the individual genetic composition has been extensively studied, and several susceptibility genes related to immune pathways that participate in SLE pathogenesis have been identified. It has been proposed that SLE takes place when susceptibility factors interact with environmental stimuli leading to a deregulated immune response. Experimental evidence suggests that such events are related to the failure of T-cell and B-cell suppression mediated by defects in cell signalling, immune tolerance and apoptotic mechanism promoting autoimmunity. In addition, it has been reported that dendritic cells (DCs) from SLE patients, which are crucial in the modulation of peripheral tolerance to self-antigens, show an increased ratio of activating/inhibitory receptors on their surfaces. This phenotype and an augmented expression of co-stimulatory molecules is thought to be critical for disease pathogenesis. Accordingly, tolerogenic DCs can be a potential strategy for developing antigen-specific therapies to reduce detrimental inflammation without causing systemic immunosuppression. In this review article we discuss the most relevant data relative to the contribution of DCs to the triggering of SLE.
Fil: Mackern Oberti, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina. Pontificia Universidad Católica de Chile; Chile
Fil: Llanos, Carolina. Pontificia Universidad Católica de Chile; Chile
Fil: Riedel, Claudia A.. Universidad Andrés Bello; Chile
Fil: Bueno, Susan M.. Pontificia Universidad Católica de Chile; Chile
Fil: Kalergis, Alexis M.. Pontificia Universidad Católica de Chile; Chile - Materia
-
DENDRITIC CELLS
IMMUNE TOLERANCE
IMMUNOTHERAPY
LUPUS
SYSTEMIC AUTOIMMUNITY - 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:11336/210319
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Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus ErythematosusMackern Oberti, Juan PabloLlanos, CarolinaRiedel, Claudia A.Bueno, Susan M.Kalergis, Alexis M.DENDRITIC CELLSIMMUNE TOLERANCEIMMUNOTHERAPYLUPUSSYSTEMIC AUTOIMMUNITYhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Systemic lupus erythematosus (SLE) is a heterogeneous disease in which excessive inflammation, autoantibodies and complement activation lead to multisystem tissue damage. The contribution of the individual genetic composition has been extensively studied, and several susceptibility genes related to immune pathways that participate in SLE pathogenesis have been identified. It has been proposed that SLE takes place when susceptibility factors interact with environmental stimuli leading to a deregulated immune response. Experimental evidence suggests that such events are related to the failure of T-cell and B-cell suppression mediated by defects in cell signalling, immune tolerance and apoptotic mechanism promoting autoimmunity. In addition, it has been reported that dendritic cells (DCs) from SLE patients, which are crucial in the modulation of peripheral tolerance to self-antigens, show an increased ratio of activating/inhibitory receptors on their surfaces. This phenotype and an augmented expression of co-stimulatory molecules is thought to be critical for disease pathogenesis. Accordingly, tolerogenic DCs can be a potential strategy for developing antigen-specific therapies to reduce detrimental inflammation without causing systemic immunosuppression. In this review article we discuss the most relevant data relative to the contribution of DCs to the triggering of SLE.Fil: Mackern Oberti, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina. Pontificia Universidad Católica de Chile; ChileFil: Llanos, Carolina. Pontificia Universidad Católica de Chile; ChileFil: Riedel, Claudia A.. Universidad Andrés Bello; ChileFil: Bueno, Susan M.. Pontificia Universidad Católica de Chile; ChileFil: Kalergis, Alexis M.. Pontificia Universidad Católica de Chile; ChileWiley Blackwell Publishing, Inc2015-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/210319Mackern Oberti, Juan Pablo; Llanos, Carolina; Riedel, Claudia A.; Bueno, Susan M.; Kalergis, Alexis M.; Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus; Wiley Blackwell Publishing, Inc; Immunology; 146; 4; 7-2015; 497-5070019-2805CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.onlinelibrary.wiley.com/journal.1365-2567.htmlinfo:eu-repo/semantics/altIdentifier/doi/10.1111/imm.12504info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:40:16Zoai:ri.conicet.gov.ar:11336/210319instacron: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:34982025-09-29 10:40:16.455CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus |
title |
Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus |
spellingShingle |
Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus Mackern Oberti, Juan Pablo DENDRITIC CELLS IMMUNE TOLERANCE IMMUNOTHERAPY LUPUS SYSTEMIC AUTOIMMUNITY |
title_short |
Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus |
title_full |
Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus |
title_fullStr |
Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus |
title_full_unstemmed |
Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus |
title_sort |
Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus |
dc.creator.none.fl_str_mv |
Mackern Oberti, Juan Pablo Llanos, Carolina Riedel, Claudia A. Bueno, Susan M. Kalergis, Alexis M. |
author |
Mackern Oberti, Juan Pablo |
author_facet |
Mackern Oberti, Juan Pablo Llanos, Carolina Riedel, Claudia A. Bueno, Susan M. Kalergis, Alexis M. |
author_role |
author |
author2 |
Llanos, Carolina Riedel, Claudia A. Bueno, Susan M. Kalergis, Alexis M. |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
DENDRITIC CELLS IMMUNE TOLERANCE IMMUNOTHERAPY LUPUS SYSTEMIC AUTOIMMUNITY |
topic |
DENDRITIC CELLS IMMUNE TOLERANCE IMMUNOTHERAPY LUPUS SYSTEMIC AUTOIMMUNITY |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Systemic lupus erythematosus (SLE) is a heterogeneous disease in which excessive inflammation, autoantibodies and complement activation lead to multisystem tissue damage. The contribution of the individual genetic composition has been extensively studied, and several susceptibility genes related to immune pathways that participate in SLE pathogenesis have been identified. It has been proposed that SLE takes place when susceptibility factors interact with environmental stimuli leading to a deregulated immune response. Experimental evidence suggests that such events are related to the failure of T-cell and B-cell suppression mediated by defects in cell signalling, immune tolerance and apoptotic mechanism promoting autoimmunity. In addition, it has been reported that dendritic cells (DCs) from SLE patients, which are crucial in the modulation of peripheral tolerance to self-antigens, show an increased ratio of activating/inhibitory receptors on their surfaces. This phenotype and an augmented expression of co-stimulatory molecules is thought to be critical for disease pathogenesis. Accordingly, tolerogenic DCs can be a potential strategy for developing antigen-specific therapies to reduce detrimental inflammation without causing systemic immunosuppression. In this review article we discuss the most relevant data relative to the contribution of DCs to the triggering of SLE. Fil: Mackern Oberti, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina. Pontificia Universidad Católica de Chile; Chile Fil: Llanos, Carolina. Pontificia Universidad Católica de Chile; Chile Fil: Riedel, Claudia A.. Universidad Andrés Bello; Chile Fil: Bueno, Susan M.. Pontificia Universidad Católica de Chile; Chile Fil: Kalergis, Alexis M.. Pontificia Universidad Católica de Chile; Chile |
description |
Systemic lupus erythematosus (SLE) is a heterogeneous disease in which excessive inflammation, autoantibodies and complement activation lead to multisystem tissue damage. The contribution of the individual genetic composition has been extensively studied, and several susceptibility genes related to immune pathways that participate in SLE pathogenesis have been identified. It has been proposed that SLE takes place when susceptibility factors interact with environmental stimuli leading to a deregulated immune response. Experimental evidence suggests that such events are related to the failure of T-cell and B-cell suppression mediated by defects in cell signalling, immune tolerance and apoptotic mechanism promoting autoimmunity. In addition, it has been reported that dendritic cells (DCs) from SLE patients, which are crucial in the modulation of peripheral tolerance to self-antigens, show an increased ratio of activating/inhibitory receptors on their surfaces. This phenotype and an augmented expression of co-stimulatory molecules is thought to be critical for disease pathogenesis. Accordingly, tolerogenic DCs can be a potential strategy for developing antigen-specific therapies to reduce detrimental inflammation without causing systemic immunosuppression. In this review article we discuss the most relevant data relative to the contribution of DCs to the triggering of SLE. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-07 |
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/11336/210319 Mackern Oberti, Juan Pablo; Llanos, Carolina; Riedel, Claudia A.; Bueno, Susan M.; Kalergis, Alexis M.; Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus; Wiley Blackwell Publishing, Inc; Immunology; 146; 4; 7-2015; 497-507 0019-2805 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/210319 |
identifier_str_mv |
Mackern Oberti, Juan Pablo; Llanos, Carolina; Riedel, Claudia A.; Bueno, Susan M.; Kalergis, Alexis M.; Contribution of Dendritic cells to the autoimmune pathology of Systemic Lupus Erythematosus; Wiley Blackwell Publishing, Inc; Immunology; 146; 4; 7-2015; 497-507 0019-2805 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://www.onlinelibrary.wiley.com/journal.1365-2567.html info:eu-repo/semantics/altIdentifier/doi/10.1111/imm.12504 |
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 |
Wiley Blackwell Publishing, Inc |
publisher.none.fl_str_mv |
Wiley Blackwell Publishing, Inc |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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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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13.070432 |