TY - JOUR
T1 - COVID-19 and antiphospholipid antibodies
T2 - A position statement and management guidance from AntiPhospholipid Syndrome Alliance for Clinical Trials and InternatiOnal Networking (APS ACTION)
AU - on Behalf of APS ACTION
AU - Wang, Xin
AU - Gkrouzman, Elena
AU - Andrade, Danieli Castro Oliveira
AU - Andreoli, Laura
AU - Barbhaiya, Medha
AU - Belmont, H. Michael
AU - Branch, David Ware
AU - de Jesús, Guilherme R.
AU - Efthymiou, Maria
AU - Ríos-Garcés, Roberto
AU - Gerosa, Maria
AU - El Hasbani, Georges
AU - Knight, Jason
AU - Meroni, Pier Luigi
AU - Pazzola, Giulia
AU - Petri, Michelle
AU - Rand, Jacob
AU - Salmon, Jane
AU - Tektonidou, Maria
AU - Tincani, Angela
AU - Uthman, Imad W.
AU - Zuily, Stephane
AU - Zuo, Yu
AU - Lockshin, Michael
AU - Cohen, Hannah
AU - Erkan, Doruk
N1 - Publisher Copyright:
© The Author(s) 2021.
PY - 2021/12
Y1 - 2021/12
N2 - Coronavirus disease 2019 (COVID-19) is associated with a high rate of thrombosis. Prolonged activated partial thromboplastin times (aPTT) and antiphospholipid antibodies (aPL) are reported in COVID-19 patients. The majority of publications have not reported whether patients develop clinically relevant persistent aPL, and the clinical significance of new aPL-positivity in COVID-19 is currently unknown. However, the reports of aPL-positivity in COVID-19 raised the question whether common mechanisms exist in the pathogenesis of COVID-19 and antiphospholipid syndrome (APS). In both conditions, thrombotic microangiopathy resulting in microvascular injury and thrombosis is hypothesized to occur through multiple pathways, including endothelial damage, complement activation, and release of neutrophil extracellular traps (NETosis). APS-ACTION, an international APS research network, created a COVID-19 working group that reviewed common mechanisms, positive aPL tests in COVID-19 patients, and implications of COVID-19 infection for patients with known aPL positivity or APS, with the goals of proposing guidance for clinical management and monitoring of aPL-positive COVID-19 patients. This guidance also serves as a call and focus for clinical and basic scientific research.
AB - Coronavirus disease 2019 (COVID-19) is associated with a high rate of thrombosis. Prolonged activated partial thromboplastin times (aPTT) and antiphospholipid antibodies (aPL) are reported in COVID-19 patients. The majority of publications have not reported whether patients develop clinically relevant persistent aPL, and the clinical significance of new aPL-positivity in COVID-19 is currently unknown. However, the reports of aPL-positivity in COVID-19 raised the question whether common mechanisms exist in the pathogenesis of COVID-19 and antiphospholipid syndrome (APS). In both conditions, thrombotic microangiopathy resulting in microvascular injury and thrombosis is hypothesized to occur through multiple pathways, including endothelial damage, complement activation, and release of neutrophil extracellular traps (NETosis). APS-ACTION, an international APS research network, created a COVID-19 working group that reviewed common mechanisms, positive aPL tests in COVID-19 patients, and implications of COVID-19 infection for patients with known aPL positivity or APS, with the goals of proposing guidance for clinical management and monitoring of aPL-positive COVID-19 patients. This guidance also serves as a call and focus for clinical and basic scientific research.
KW - Antiphospholipid antibodies
KW - COVID-19
KW - Hughes syndrome
KW - anticoagulation
KW - antiphospholipid syndrome
KW - lupus anticoagulant
KW - thrombosis
UR - http://www.scopus.com/inward/record.url?scp=85121840181&partnerID=8YFLogxK
U2 - 10.1177/09612033211062523
DO - 10.1177/09612033211062523
M3 - Article
C2 - 34915764
AN - SCOPUS:85121840181
SN - 0961-2033
VL - 30
SP - 2276
EP - 2285
JO - Lupus
JF - Lupus
IS - 14
ER -