C1-esterase inhibitor enhances thrombin generation and spatial fibrin clot propagation in the presence of thrombomodulin

• Published in: Thrombosis research 2019-04, Vol.176, p.54-60
• Main Authors: Tarandovskiy, Ivan D., Buehler, Paul W., Ataullakhanov, Fazoil I., Karnaukhova, Elena
• Format: Article
• Language: English
• Subjects: Blood Coagulation; C1-inhibitor; Complement C1 Inhibitor Protein - analysis; Complement C1 Inhibitor Protein - metabolism; Fibrin - analysis; Fibrin - metabolism; Hereditary angioedem; Humans; Protein C; Thrombin - analysis; Thrombin - metabolism; Thrombin generation; Thrombodynamics; Thrombomodulin; Thrombomodulin - analysis; Thrombomodulin - metabolism; Thrombosis - blood; Thrombosis - metabolism
• ISSN: 0049-3848; 1879-2472
• DOI: 10.1016/j.thromres.2019.02.013

Package inserts for C1-esterase inhibitor (C1INH) products include warnings for an elevated risk of possible thrombosis in certain individuals, referring to thromboembolic events (TEEs) that were reported to occur after C1INH infusions. However, the mechanism(s) that could explain possible development of TEEs due to C1INH remains unknown. In this work, we evaluated plausible impact of C1INH on the protein C (PC) anticoagulant system. We performed thrombin generation (TG) assays (TGA) and analyzed spatial fibrin clot propagation using thrombodynamics in plasma of individual donors after the addition of thrombomodulin (TM) and C1INH. The addition of C1INH was consistent with the plasma concentrations resulting from doses currently approved for the HAE treatment up to ones consistent with off-label use in patients with risk of inflammation. 16 IU/ml of C1INH significantly enhanced thrombin peak (TP) generation in the presence of 12 and 15 nM TM. TG enhancement was observed by the addition of C1INH to make concentrations equal to 2 and 4 IU/ml in some donor plasmas. C1INH addition in the presence of TM enhanced the stop time of spatial clot growth in Thrombodynamics assay. A chromogenic activity assay demonstrated that C1INH inhibited PC activation by thrombin in the presence of TM. Substitution of TM with APC in TGA attenuated the TP enhancing effect of C1INH. The collective results of the present study suggest a concentration dependent C1INH interaction with the PC system. This study introduces a plausible TM-dependent mechanism, that may explain reported TEEs via suppressed production of APC in the presence of C1INH. •A possibility of elevated risk of thrombosis was reported for plasma-derived C1-inhibitor products•Mechanism of thrombosis induced by C1-inhibitor are presented•C1-inhibitor can enhance thrombin generation in the presence of thrombomodulin•The enhancement of thrombin generation by C1-inhibitor is strictly donor specific•C1-inhibitor reduces protein C activation by thrombin-thrombomodulin complex