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DOI: 10.1160/TH16-12-0911
Platelet receptors as therapeutic targets: Past, present and future
Financial Support: SG is supported by grants from Scientific Research in Japan (24390202,050452092), a grant for the next-generation supercomputer Research and Development program supported by RIKEN a grant for Biomedical Engineering Research from the Nakatani Foundation of measuring technologies in biomedical engineering, Sanofi, and Pfizer. KP is supported by a Principal Research Fellowship of the National Health and Medical Research Council of Australia. WS is supported by grants from the Bayerische Forschungsstiftung (AZ 1145–14), the Deutsche Forschungsgemeinschaft (SFB1123/B08), and the August-Lenz foundation.Publication History
Received:
05 December 2016
Accepted after major revision:
08 April 2017
Publication Date:
28 November 2017 (online)
Summary
Anti-platelet drugs reduce arterial thrombosis after plaque rupture and erosion, prevent stent thrombosis and are used to prevent and treat myocardial infarction and ischaemic stroke. Some of them may also be helpful in treating less frequent diseases such as thrombotic thrombocytopenic purpura. The present concise review aims to cover current and future developments of anti-platelet drugs interfering with the interaction of von Willebrand factor (VWF) with glycoprotein (GP) Ibα, and directed against GPVI, GPIIb/IIIa (integrin αIIbβ3), the thrombin receptor PAR-1, and the ADP receptor P2Y12. The high expectations of having novel antiplatelet drugs which selectively inhibit arterial thrombosis without interfering with normal haemostasis could possibly be met in the near future.
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