Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?

ABSTRACT: Antiphospholipid syndrome (APS) is an autoimmune disease characterized by the presence of thrombosis and/or obstetric events, and persistent high titers of circulating antiphospholipid antibodies (aPL). Most patients display both clinical signs, although some patients can have isolated vas...

Full description

Autores:
Cadavid Jaramillo, Ángela Patricia
Tipo de recurso:
http://purl.org/coar/resource_type/c_5794
Fecha de publicación:
2022
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/31532
Acceso en línea:
https://hdl.handle.net/10495/31532
Palabra clave:
Síndrome Antifosfolípido
Antiphospholipid Syndrome
Anticuerpos Antifosfolípidos
Antibodies, Antiphospholipid
Trombosis de la Vena
Venous Thrombosis
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-sa/2.5/co/
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repository_id_str
dc.title.spa.fl_str_mv Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?
title Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?
spellingShingle Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?
Síndrome Antifosfolípido
Antiphospholipid Syndrome
Anticuerpos Antifosfolípidos
Antibodies, Antiphospholipid
Trombosis de la Vena
Venous Thrombosis
title_short Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?
title_full Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?
title_fullStr Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?
title_full_unstemmed Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?
title_sort Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?
dc.creator.fl_str_mv Cadavid Jaramillo, Ángela Patricia
dc.contributor.author.none.fl_str_mv Cadavid Jaramillo, Ángela Patricia
dc.contributor.conferencename.spa.fl_str_mv Latin American and Caribbean Congress of Immunology ALACI 2022 (13 : 7 de junio de 2022 : Varadero, Matanzas, Cuba)
dc.contributor.researchgroup.spa.fl_str_mv Grupo de Investigación en Trombosis
Grupo Reproducción
dc.subject.decs.none.fl_str_mv Síndrome Antifosfolípido
Antiphospholipid Syndrome
Anticuerpos Antifosfolípidos
Antibodies, Antiphospholipid
Trombosis de la Vena
Venous Thrombosis
topic Síndrome Antifosfolípido
Antiphospholipid Syndrome
Anticuerpos Antifosfolípidos
Antibodies, Antiphospholipid
Trombosis de la Vena
Venous Thrombosis
description ABSTRACT: Antiphospholipid syndrome (APS) is an autoimmune disease characterized by the presence of thrombosis and/or obstetric events, and persistent high titers of circulating antiphospholipid antibodies (aPL). Most patients display both clinical signs, although some patients can have isolated vascular or obstetric variants. aPL are a heterogeneous group of autoantibodies directed against negatively charged phospholipids or phospholipid-binding proteins. It seems that the same aPL are present in the two clinical manifestations of APS, but it is evident that vascular APS and obstetric APS have different pathogenic mechanisms, the first being caused by a state of hypercoagulability and the second by an inflammatory phenomenon. It is not yet clear if there are different specificities of these aPL. Sera or polyclonal IgG from women with several clinical manifestations of APS show differential effects on various cellular models in in vitro assays. On trophoblast cells there is a decrease of trophoblast invasion. On endothelial cells these aPL stimulated nitrotyrosine expression, reduction in eNOS phosphorylation at Ser1177, mitochondrial hyperpolarization and activation of autophagic pathways, expression of adhesion molecules and the generation of procoagulant microparticles. In conclusion, whether vascular APS and obstetric APS are two sides of the same coin, or two different coins altogether, has not yet been clarified. It would be very useful both for the diagnosis and for the therapeutic approach of the patients to define whether the determining factors of each variant of the disease are the aPL per se or whether there are other factors that influence the onset and pathogenesis of obstetric or vascular APS.
publishDate 2022
dc.date.accessioned.none.fl_str_mv 2022-10-28T13:55:33Z
dc.date.available.none.fl_str_mv 2022-10-28T13:55:33Z
dc.date.issued.none.fl_str_mv 2022-06-07
dc.type.spa.fl_str_mv Documento de conferencia
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_c94f
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dc.language.iso.spa.fl_str_mv eng
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dc.relation.conferencedate.spa.fl_str_mv 2022-06-06/2022-06-10
dc.relation.conferenceplace.spa.fl_str_mv Meliá Internacional Varadero, Varadero, Matanzas, Cuba
dc.relation.ispartofjournal.spa.fl_str_mv ALACI22 - 13th Latin American and Caribbean Immunology and 7th Cuban Immunology Society Congresses
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spelling Cadavid Jaramillo, Ángela PatriciaLatin American and Caribbean Congress of Immunology ALACI 2022 (13 : 7 de junio de 2022 : Varadero, Matanzas, Cuba)Grupo de Investigación en TrombosisGrupo Reproducción2022-10-28T13:55:33Z2022-10-28T13:55:33Z2022-06-07https://hdl.handle.net/10495/31532ABSTRACT: Antiphospholipid syndrome (APS) is an autoimmune disease characterized by the presence of thrombosis and/or obstetric events, and persistent high titers of circulating antiphospholipid antibodies (aPL). Most patients display both clinical signs, although some patients can have isolated vascular or obstetric variants. aPL are a heterogeneous group of autoantibodies directed against negatively charged phospholipids or phospholipid-binding proteins. It seems that the same aPL are present in the two clinical manifestations of APS, but it is evident that vascular APS and obstetric APS have different pathogenic mechanisms, the first being caused by a state of hypercoagulability and the second by an inflammatory phenomenon. It is not yet clear if there are different specificities of these aPL. Sera or polyclonal IgG from women with several clinical manifestations of APS show differential effects on various cellular models in in vitro assays. On trophoblast cells there is a decrease of trophoblast invasion. On endothelial cells these aPL stimulated nitrotyrosine expression, reduction in eNOS phosphorylation at Ser1177, mitochondrial hyperpolarization and activation of autophagic pathways, expression of adhesion molecules and the generation of procoagulant microparticles. In conclusion, whether vascular APS and obstetric APS are two sides of the same coin, or two different coins altogether, has not yet been clarified. It would be very useful both for the diagnosis and for the therapeutic approach of the patients to define whether the determining factors of each variant of the disease are the aPL per se or whether there are other factors that influence the onset and pathogenesis of obstetric or vascular APS.Universidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODIColombia. Ministerio de Ciencia Tecnología e Innovación - MinicienciasCOL0010421COL0007631application/pdfenghttp://creativecommons.org/licenses/by-nc-sa/2.5/co/https://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccessAtribución-NoComercial-CompartirIgual 2.5 Colombiahttp://purl.org/coar/access_right/c_abf2Obstetric and vascular antiphospholipid syndrome: Two sides of the same coin?Documento de conferenciahttp://purl.org/coar/resource_type/c_5794http://purl.org/coar/resource_type/c_c94fhttps://purl.org/redcol/resource_type/EChttp://purl.org/coar/version/c_b1a7d7d4d402bcceinfo:eu-repo/semantics/conferenceObjectinfo:eu-repo/semantics/draftVaradero, CubaSíndrome AntifosfolípidoAntiphospholipid SyndromeAnticuerpos AntifosfolípidosAntibodies, AntiphospholipidTrombosis de la VenaVenous Thrombosis2022-06-06/2022-06-10Meliá Internacional Varadero, Varadero, Matanzas, CubaALACI22 - 13th Latin American and Caribbean Immunology and 7th Cuban Immunology Society Congressesgrid.412881.6grid.433658.fMecanismos de daño y disfunción endotelial en el síndrome antifosfolípido: ¿hay diferencias de acuerdo a las manifestaciones clínicas del síndrome?”2015-7448 y 111580762949; 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