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- W2041194529 endingPage "176" @default.
- W2041194529 startingPage "165" @default.
- W2041194529 abstract "The antiphospholipid syndrome (APS) is an autoimmune disease characterized by the clinical features of recurrent thrombosis in the venous or arterial circulation and fetal losses. Antiphospholipid antibodies (aPL), particularly against the phospholipid binding protein beta-2 glycoprotein I (β2GPI), play an important role in APS pathological mechanisms. aPL can activate intracellular signal transduction in a β2GPI-dependent manner to induce inflammatory responses, and promote hypercoagulable state and recurrent spontaneous abortion when β2GPI is associated with the cell surface receptor. In vivo and in vitro studies show that Annexin A2 (ANXA2) is the high affinity receptor that connects β2GPI to the target cells. However, ANXA2 is not a transmembrane protein and lacks an intracellular signal transduction pathway. Growing evidences suggest that the transmembrane protein toll-like receptor 4 (TLR4) might act as an 'adaptor' for intracellular signal transduction. This review focuses on the role of TLR4 and its signalling pathway in APS pathological mechanisms which will help us better understand the pathological processes of this syndrome." @default.
- W2041194529 created "2016-06-24" @default.
- W2041194529 creator A5006873847 @default.
- W2041194529 creator A5008118059 @default.
- W2041194529 creator A5044440736 @default.
- W2041194529 creator A5061883832 @default.
- W2041194529 date "2013-10-08" @default.
- W2041194529 modified "2023-10-04" @default.
- W2041194529 title "The role of TLR4 in pathophysiology of antiphospholipid syndrome-associated thrombosis and pregnancy morbidity" @default.
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