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An update on the biologics for the treatment of antiphospholipid syndrome

Antiphospholipid syndrome (APS) is a systemic autoimmune disease characterized by thrombosis and pregnancy morbidity with the persistent presence of antiphospholipid antibodies (aPLs). Although anticoagulation is the primary treatment for APS, it fails in approximately 20-30% of obstetric APS cases...

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Detalles Bibliográficos
Autores principales: Yun, Zelin, Duan, Lizhi, Liu, Xiangjun, Cai, Qingmeng, Li, Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10237350/
https://www.ncbi.nlm.nih.gov/pubmed/37275894
http://dx.doi.org/10.3389/fimmu.2023.1145145
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author Yun, Zelin
Duan, Lizhi
Liu, Xiangjun
Cai, Qingmeng
Li, Chun
author_facet Yun, Zelin
Duan, Lizhi
Liu, Xiangjun
Cai, Qingmeng
Li, Chun
author_sort Yun, Zelin
collection PubMed
description Antiphospholipid syndrome (APS) is a systemic autoimmune disease characterized by thrombosis and pregnancy morbidity with the persistent presence of antiphospholipid antibodies (aPLs). Although anticoagulation is the primary treatment for APS, it fails in approximately 20-30% of obstetric APS cases and more than 30% of thrombotic APS cases. Therefore, there is a need for new, targeted treatments beyond anticoagulants. Biologics, such as rituximab and eculizumab, have been recommended for refractory catastrophic APS. This review focuses on the recent advancements in the pathogenesis of APS and explores the potential of targeted treatments, including eculizumab, rituximab, belimumab, daratumumab, obinutuzumab, and anti-TNF-α antibodies, for APS management.
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spelling pubmed-102373502023-06-03 An update on the biologics for the treatment of antiphospholipid syndrome Yun, Zelin Duan, Lizhi Liu, Xiangjun Cai, Qingmeng Li, Chun Front Immunol Immunology Antiphospholipid syndrome (APS) is a systemic autoimmune disease characterized by thrombosis and pregnancy morbidity with the persistent presence of antiphospholipid antibodies (aPLs). Although anticoagulation is the primary treatment for APS, it fails in approximately 20-30% of obstetric APS cases and more than 30% of thrombotic APS cases. Therefore, there is a need for new, targeted treatments beyond anticoagulants. Biologics, such as rituximab and eculizumab, have been recommended for refractory catastrophic APS. This review focuses on the recent advancements in the pathogenesis of APS and explores the potential of targeted treatments, including eculizumab, rituximab, belimumab, daratumumab, obinutuzumab, and anti-TNF-α antibodies, for APS management. Frontiers Media S.A. 2023-05-19 /pmc/articles/PMC10237350/ /pubmed/37275894 http://dx.doi.org/10.3389/fimmu.2023.1145145 Text en Copyright © 2023 Yun, Duan, Liu, Cai and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Yun, Zelin
Duan, Lizhi
Liu, Xiangjun
Cai, Qingmeng
Li, Chun
An update on the biologics for the treatment of antiphospholipid syndrome
title An update on the biologics for the treatment of antiphospholipid syndrome
title_full An update on the biologics for the treatment of antiphospholipid syndrome
title_fullStr An update on the biologics for the treatment of antiphospholipid syndrome
title_full_unstemmed An update on the biologics for the treatment of antiphospholipid syndrome
title_short An update on the biologics for the treatment of antiphospholipid syndrome
title_sort update on the biologics for the treatment of antiphospholipid syndrome
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10237350/
https://www.ncbi.nlm.nih.gov/pubmed/37275894
http://dx.doi.org/10.3389/fimmu.2023.1145145
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