| Autor: |
Assaf A, Barg, Tami, Brutman-Barazani, Einat, Avishai, Ivan, Budnik, Omri, Cohen, Rima, Dardik, Sarina, Levy-Mendelovich, Tami, Livnat, Gili, Kenet |
| Rok vydání: |
2022 |
| Předmět: |
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| Zdroj: |
Blood Cells, Molecules, and Diseases. 95:102663 |
| ISSN: |
1079-9796 |
| DOI: |
10.1016/j.bcmd.2022.102663 |
| Popis: |
Rare bleeding disorders (RBD) are inherited coagulopathies, whose hemostatic control is based upon replacement therapy. Marstacimab (PF-06741086) is a human monoclonal IgG that targets the Kunitz2 domain of tissue factor pathway inhibitor [TFPI]. Marstacimab is currently in development for bleeding prophylaxis in patients with hemophilia.To assess the potential impact of Marstacimab upon thrombin generation (TG) in RBD patients' plasma samples.Our cohort included 18 RBD patients, with severe deficiencies: 5 Von Willebrand Disease (VWD) type 3, 4 FVII, 3 FXI, 2 FXIII deficiency and 1 patient with: FX, FV + FVIII, Fibrinogen, combined vitamin K dependent factors' deficiency. Citrated samples from RBD patients were collected and spiked with Marstacimab, TG was measured by calibrated automated thrombogram. Among all patients a reduced baseline TG was observed as compared to controls. Improvement of median (lag time, peak and ETP was observed in Marstacimab spiked samples from 8 min, 99 nM, 1116 nMx min to 5.5 min, 194 nM,1614 nMx min, respectively. None of the values measured among RBD patients exceeded normal controls.These in vitro data suggest that Marstacimab may serve as a promising approach for restoring the hemostatic balance in various RBD, though potential clinical implications should be further investigated. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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