Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10495/43625
Título : Effects of anti-beta 2-glycoprotein 1 antibodies and its association with pregnancy-related morbidity in antiphospholipid syndrome
Autor : Cadavid Jaramillo, Angela Patricia
Velásquez Berrio, Manuela
Fierro Martínez, Juan José
de Leeuw, Karina
metadata.dc.subject.*: Síndrome Antifosfolípido
Antiphospholipid Syndrome
Autoanticuerpos
Autoantibodies
Embarazo
Pregnancy
Pregnancy Complications
Complicaciones del Embarazo
beta 2-Glycoproteína I
beta 2 Glicoprotein I
https://id.nlm.nih.gov/mesh/D016736
https://id.nlm.nih.gov/mesh/D001323
https://id.nlm.nih.gov/mesh/D011247
https://id.nlm.nih.gov/mesh/D011248
https://id.nlm.nih.gov/mesh/D053482
Fecha de publicación : 2022
Editorial : Wiley-Blackwell
Citación : Fierro JJ, Velásquez M, Cadavid AP, de Leeuw K. Effects of anti-beta 2-glycoprotein 1 antibodies and its association with pregnancy-related morbidity in antiphospholipid syndrome. Am J Reprod Immunol. 2022 Jan;87(1):e13509. doi: 10.1111/aji.13509.
Resumen : ABSTRACT: Antiphospholipid syndrome (APS) is an autoimmune disease characterized by venous, arterial, or small-vessel thrombosis and/or pregnancy-related morbidity, associated with persistent positivity of antiphospholipid antibodies (aPL). Pregnancy-related morbidity in APS patients is characterized by unexplained fetal deaths, premature birth of morphologically normal newborns, and/or consecutive pregnancy losses before the 10th week of gestation. Beta 2-glycoprotein 1 (ß2GP1) is the main antigen recognized by aPL and plays an essential role in the pathogenesis of APS. Antibodies against ß2GP1 (aß2GP1) are involved in damage-generating mechanisms in APS due to their interaction with trophoblasts, decidua, and endothelial cells. aß2GP1 might be used as a prognostic tool for obstetric risk stratification and ß2GP1 could be a target for molecular-targeted treatment to prevent pregnancy morbidity in APS. This review describes these aspects of aß2GP1, including effects on different cellular targets, its association with the severity of obstetric manifestations and the potential of ß2GP1-targeted therapies for APS.
metadata.dc.identifier.eissn: 1600-0897
ISSN : 1046-7408
metadata.dc.identifier.doi: 10.1111/aji.13509
metadata.dc.identifier.url: http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-0897
Aparece en las colecciones: Artículos de Revista en Ciencias Médicas

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