Abstract |
Antiphospholipid syndrome (APS) is an autoimmune disease characterized by arterial, venous or small-vessel thrombotic events, and recurrent miscarriages or fetal loss. APS diagnosis is based on the repeated detection of anti- phospholipid (PL) antibodies (Ab), typically associated with anti-β2 glycoprotein I (β2GPI)-Ab. Recent studies suggest that anti-β2GPI Ab activity involves a protein complex including β2GPI and annexin A2 (ANXA2). Anti-ANXA2 Ab recognizes this complex, and these Ab can effectively promote thrombosis by inhibiting plasmin generation, and by activating endothelial cells. Therefore, anti-ANXA2 Ab represent a new biomarker, which can be detected in up to 25% of APS patients. Moreover, anti-ANXA2 Ab have been detected, in thrombotic associated diseases including pre-eclampsia, in other autoimmune diseases, and in cancer.
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Authors | Felipe Cañas, Laurent Simonin, Francis Couturaud, Yves Renaudineau |
Journal | Thrombosis research
(Thromb Res)
Vol. 135
Issue 2
Pg. 226-30
(Feb 2015)
ISSN: 1879-2472 [Electronic] United States |
PMID | 25533130
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2014 Elsevier Ltd. All rights reserved. |
Chemical References |
- Annexin A2
- Autoantibodies
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Topics |
- Annexin A2
(metabolism)
- Antiphospholipid Syndrome
(immunology)
- Autoantibodies
(immunology)
- Autoimmune Diseases
(immunology)
- Humans
- Thrombosis
(immunology)
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