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Thromb Haemost 2019; 119(08): 1212-1221
DOI: 10.1055/s-0039-1687877
DOI: 10.1055/s-0039-1687877
Theme Issue Article
Btk Inhibitors as First Oral Atherothrombosis-Selective Antiplatelet Drugs?
Funding This study was supported by grants from the Deutsche Forschungsgemeinschaft (SFB1123/B08) and the August-Lenz foundation.Weitere Informationen
Publikationsverlauf
29. September 2018
09. März 2019
Publikationsdatum:
14. Mai 2019 (online)
Abstract
Bruton's tyrosine kinase (Btk) is essential for B cell differentiation and proliferation, but also platelets express Btk. Patients with X-linked agammaglobulinemia due to hereditary Btk deficiency do not show bleeding, but a mild bleeding tendency is observed in high dose therapy of B-cell malignancies with ibrutinib and novel second-generation irreversible Btk inhibitors (acalabrutinib and ONO/GS-4059). This review discusses recent studies that may explain this apparent paradox and gives mechanistic insights that suggest a unique potential of low dose irreversible Btk inhibitors as atherothrombosis-focused antiplatelet drugs.
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