TY - JOUR
T1 - Treatment of antiphospholipid syndrome beyond anticoagulation
AU - Dobrowolski, Chrisanna
AU - Erkan, Doruk
N1 - Funding Information:
Doruk Erkan received research grants from New York Community Trust, Hospital for Special Surgery Medical Education Academy, Lupus Clinical Trials Consortium, and National Heart Lung and Blood Institute (NHLBI); is a clinical trial investigator for EMD Serono, GSK, and Xencor; and is a consultant for GSK and Ablynx.
Publisher Copyright:
© 2018
PY - 2019/9
Y1 - 2019/9
N2 - Antiphospholipid syndrome (APS) is a systemic autoimmune disorder marked by thrombosis and/or pregnancy morbidity in the presence of antiphospholipid antibodies (aPL). At the present time, treatment is primarily focused on anticoagulation. However, there is increasing awareness of the mechanisms involved in APS pathogenesis, which has led to the trial of novel therapies targeting those mechanisms. Following a brief review of the etiopathogenesis of and current management strategies in APS, this paper focuses on the evidence for these potential, targeted APS treatments, e.g., hydroxychloroquine, statins, rituximab, belimumab, eculizumab, defibrotide, sirolimus, and peptide therapy.
AB - Antiphospholipid syndrome (APS) is a systemic autoimmune disorder marked by thrombosis and/or pregnancy morbidity in the presence of antiphospholipid antibodies (aPL). At the present time, treatment is primarily focused on anticoagulation. However, there is increasing awareness of the mechanisms involved in APS pathogenesis, which has led to the trial of novel therapies targeting those mechanisms. Following a brief review of the etiopathogenesis of and current management strategies in APS, this paper focuses on the evidence for these potential, targeted APS treatments, e.g., hydroxychloroquine, statins, rituximab, belimumab, eculizumab, defibrotide, sirolimus, and peptide therapy.
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U2 - 10.1016/j.clim.2018.03.001
DO - 10.1016/j.clim.2018.03.001
M3 - Article
C2 - 29510235
AN - SCOPUS:85046106427
SN - 1521-6616
VL - 206
SP - 53
EP - 62
JO - Clinical Immunology
JF - Clinical Immunology
ER -