Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical Manifestations

ABSTRACT: The endothelium is a monolayer of cells that covers the inner surface of blood vessels and its integrity is essential for the maintenance of vascular health. Endothelial dysfunction is a key pathological component of antiphospholipid syndrome (APS). Its systemic complications include throm...

Full description

Autores:
Velásquez Berrio, Manuela
Rojas López, Mauricio
Abrahams, Vikki M
Escudero, Carlos Alonso
Cadavid Jaramillo, Angela Patricia
Tipo de recurso:
Review article
Fecha de publicación:
2018
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/34187
Acceso en línea:
https://hdl.handle.net/10495/34187
https://www.frontiersin.org/articles/10.3389/fphys.2018.01840/full
Palabra clave:
Antibodies, Antiphospholipid
Anticuerpos Antifosfolípidos
Inflammation
Inflamación
Thrombosis
Trombosis
Antiphospholipid Syndrome
Síndrome Antifosfolípido
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical Manifestations
title Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical Manifestations
spellingShingle Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical Manifestations
Antibodies, Antiphospholipid
Anticuerpos Antifosfolípidos
Inflammation
Inflamación
Thrombosis
Trombosis
Antiphospholipid Syndrome
Síndrome Antifosfolípido
title_short Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical Manifestations
title_full Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical Manifestations
title_fullStr Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical Manifestations
title_full_unstemmed Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical Manifestations
title_sort Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical Manifestations
dc.creator.fl_str_mv Velásquez Berrio, Manuela
Rojas López, Mauricio
Abrahams, Vikki M
Escudero, Carlos Alonso
Cadavid Jaramillo, Angela Patricia
dc.contributor.author.none.fl_str_mv Velásquez Berrio, Manuela
Rojas López, Mauricio
Abrahams, Vikki M
Escudero, Carlos Alonso
Cadavid Jaramillo, Angela Patricia
dc.contributor.researchgroup.spa.fl_str_mv Grupo de Inmunología Celular e Inmunogenética
Grupo Reproducción
dc.subject.decs.none.fl_str_mv Antibodies, Antiphospholipid
Anticuerpos Antifosfolípidos
Inflammation
Inflamación
Thrombosis
Trombosis
Antiphospholipid Syndrome
Síndrome Antifosfolípido
topic Antibodies, Antiphospholipid
Anticuerpos Antifosfolípidos
Inflammation
Inflamación
Thrombosis
Trombosis
Antiphospholipid Syndrome
Síndrome Antifosfolípido
description ABSTRACT: The endothelium is a monolayer of cells that covers the inner surface of blood vessels and its integrity is essential for the maintenance of vascular health. Endothelial dysfunction is a key pathological component of antiphospholipid syndrome (APS). Its systemic complications include thrombotic endocarditis, valvular dysfunction, cerebrovascular occlusions, proliferative nephritis, deep vein thrombosis, and pulmonary embolism. In women, APS is also associated with pregnancy complications (obstetric APS). The conventional treatment regimens for APS are ineffective when the clinical symptoms are severe. Therefore, a better understanding of alterations in the endothelium caused by antiphospholipid antibodies (aPL) may lead to more effective therapies in patients with elevated aPL titers and severe clinical symptoms. Currently, while in vivo analyses of endothelial dysfunction in patients with APS have been reported, most research has been performed using in vitro models with endothelial cells exposed to either patient serum/plasma, monoclonal aPL, or IgGs isolated from patients with APS. These studies have described a reduction in endothelial cell nitric oxide synthesis, the induction of inflammatory and procoagulant phenotypes, an increase in endothelial proliferation, and impairments in vascular remodeling and angiogenesis. Despite these lines of evidence, further research is required to better understand the pathophysiology of endothelial dysfunction in patients with APS. In this review, we have compared the current understanding about the mechanisms of endothelial dysfunction induced by patient-derived aPL under the two main clinical manifestations of APS: thrombosis and gestational complications, either alone or in combination. We also discuss gaps in our current knowledge regarding aPL-induced endothelial dysfunction.
publishDate 2018
dc.date.issued.none.fl_str_mv 2018
dc.date.accessioned.none.fl_str_mv 2023-03-23T16:48:01Z
dc.date.available.none.fl_str_mv 2023-03-23T16:48:01Z
dc.type.spa.fl_str_mv Artículo de revisión
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dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/34187
dc.identifier.doi.none.fl_str_mv 10.3389/fphys.2018.01840
dc.identifier.eissn.none.fl_str_mv 1664-042X
dc.identifier.url.spa.fl_str_mv https://www.frontiersin.org/articles/10.3389/fphys.2018.01840/full
url https://hdl.handle.net/10495/34187
https://www.frontiersin.org/articles/10.3389/fphys.2018.01840/full
identifier_str_mv 10.3389/fphys.2018.01840
1664-042X
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Front Physiol
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dc.relation.citationissue.spa.fl_str_mv 1840
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 9
dc.relation.ispartofjournal.spa.fl_str_mv Frontiers in Physiology
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dc.publisher.place.spa.fl_str_mv Lausana, Suiza
dc.publisher.faculty.spa.fl_str_mv sin facultad - programa
institution Universidad de Antioquia
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spelling Velásquez Berrio, ManuelaRojas López, MauricioAbrahams, Vikki MEscudero, Carlos AlonsoCadavid Jaramillo, Angela PatriciaGrupo de Inmunología Celular e InmunogenéticaGrupo Reproducción2023-03-23T16:48:01Z2023-03-23T16:48:01Z2018https://hdl.handle.net/10495/3418710.3389/fphys.2018.018401664-042Xhttps://www.frontiersin.org/articles/10.3389/fphys.2018.01840/fullABSTRACT: The endothelium is a monolayer of cells that covers the inner surface of blood vessels and its integrity is essential for the maintenance of vascular health. Endothelial dysfunction is a key pathological component of antiphospholipid syndrome (APS). Its systemic complications include thrombotic endocarditis, valvular dysfunction, cerebrovascular occlusions, proliferative nephritis, deep vein thrombosis, and pulmonary embolism. In women, APS is also associated with pregnancy complications (obstetric APS). The conventional treatment regimens for APS are ineffective when the clinical symptoms are severe. Therefore, a better understanding of alterations in the endothelium caused by antiphospholipid antibodies (aPL) may lead to more effective therapies in patients with elevated aPL titers and severe clinical symptoms. Currently, while in vivo analyses of endothelial dysfunction in patients with APS have been reported, most research has been performed using in vitro models with endothelial cells exposed to either patient serum/plasma, monoclonal aPL, or IgGs isolated from patients with APS. These studies have described a reduction in endothelial cell nitric oxide synthesis, the induction of inflammatory and procoagulant phenotypes, an increase in endothelial proliferation, and impairments in vascular remodeling and angiogenesis. Despite these lines of evidence, further research is required to better understand the pathophysiology of endothelial dysfunction in patients with APS. In this review, we have compared the current understanding about the mechanisms of endothelial dysfunction induced by patient-derived aPL under the two main clinical manifestations of APS: thrombosis and gestational complications, either alone or in combination. We also discuss gaps in our current knowledge regarding aPL-induced endothelial dysfunction.COL000863910application/pdfengFrontiers Research FoundationLausana, Suizasin facultad - programahttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Mechanisms of Endothelial Dysfunction in Antiphospholipid Syndrome : Association With Clinical ManifestationsArtículo de revisiónhttp://purl.org/coar/resource_type/c_dcae04bchttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARTREVhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAntibodies, AntiphospholipidAnticuerpos AntifosfolípidosInflammationInflamaciónThrombosisTrombosisAntiphospholipid SyndromeSíndrome AntifosfolípidoFront Physiol10184019Frontiers in PhysiologyPublicationORIGINALVelasquezManuela_2018_MechanismsEndothelialDysfunction.pdfVelasquezManuela_2018_MechanismsEndothelialDysfunction.pdfArtículo de revisiónapplication/pdf2333905https://bibliotecadigital.udea.edu.co/bitstreams/2896b029-1234-473d-8a14-df89d4cf784e/downloada71eb7f4608281bc25ba1283db7ecd99MD51trueAnonymousREADCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8927https://bibliotecadigital.udea.edu.co/bitstreams/2c36b17e-1734-429f-a180-9f3bfb427c23/download1646d1f6b96dbbbc38035efc9239ac9cMD52falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/563c6c38-6f0b-4d51-b6ef-567e1ab964ab/download8a4605be74aa9ea9d79846c1fba20a33MD53falseAnonymousREADTEXTVelasquezManuela_2018_MechanismsEndothelialDysfunction.pdf.txtVelasquezManuela_2018_MechanismsEndothelialDysfunction.pdf.txtExtracted texttext/plain58987https://bibliotecadigital.udea.edu.co/bitstreams/03bb72b0-ecb7-4966-8113-cce55f0ebed8/download478437735e5939b7d659d72a3acc20e8MD54falseAnonymousREADTHUMBNAILVelasquezManuela_2018_MechanismsEndothelialDysfunction.pdf.jpgVelasquezManuela_2018_MechanismsEndothelialDysfunction.pdf.jpgGenerated Thumbnailimage/jpeg14214https://bibliotecadigital.udea.edu.co/bitstreams/1d77cdfb-72fd-479f-8b8c-2441ca38dff1/download1c5ac09cc712271b9a285588d051d366MD55falseAnonymousREAD10495/34187oai:bibliotecadigital.udea.edu.co:10495/341872025-03-26 21:18:37.92https://creativecommons.org/licenses/by/4.0/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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