• VLX-1005 demonstrates the potential as an effective treatment for HIT by preventing platelet activation without increasing bleeding risk. • The efficacy and safety of VLX-1005 with a direct thrombin inhibitor in patients with HIT has been evaluated in a Phase II clinical trial. Heparin-induced thrombocytopenia (HIT) is an immune prothrombotic disorder characterized by the binding of platelet-activating immunoglobulin G antibodies to platelet factor 4/heparin. In the platelet, this leads to cross-linking of the immunoreceptor tyrosine-based activation motif (ITAM) FcγRIIa, platelet activation and thrombocytopenia, which in combination with extensive thrombin generation significantly increases the risk of thrombosis. Our lab has previously demonstrated that 12-lipoxygenase (12-LOX), an oxygenase primarily expressed in the platelet, plays a critical role in platelet activation through FcγRIIa. In this study, we aimed to determine the effectiveness of VLX-1005, a potent and selective inhibitor of 12-LOX, alone or in combination with argatroban, in preventing HIT. Pre-treatment with VLX-1005 attenuated aggregation of human washed platelets stimulated with a HIT immune complex in vitro . VLX-1005 prevented ITAM-induced human whole blood impedance alone or in combination with argatroban. VLX-1005 treatment impaired platelet adhesion and accumulation on a collagen-coated surface under shear stress. Mice expressing transgenic human FcγRIIa and 12-LOX experienced severe thrombocytopenia and thrombosis following a HIT-like challenge, while mice expressing transgenic human FcγRIIa and with 12-LOX knockout were completely refractory to HIT pathology. VLX-1005 treatment did not affect coagulation nor increase the risk of bleeding. This study demonstrates that inhibition of 12-LOX might be an effective intervention for prevention of ITAM-regulated platelet activation, such as in HIT, and is independent of argatroban effects in the blood. Importantly, VLX-1005 prevents platelet activation and does not increase the bleeding risk associated with direct thrombin inhibitors, such as argatroban.
Yamaguchi et al. (Sun,) studied this question.