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A bispecific antibody approach for the potential prophylactic treatment of inherited bleeding disorders.

Prafull S GandhiMinka ZivkovicHenrik ØstergaardAmalie C BondeTorben ElmMonika N LøvgreenGerd SchluckebierEva JohanssonOle H OlsenEva H N OlsenIan-Arris de BusKarien BloemOskar AlskärCatherine J ReaSøren E BjørnRoger E G SchutgensBenny SørensenRolf T UrbanusJohan H Faber
Published in: Nature cardiovascular research (2024)
Inherited bleeding disorders such as Glanzmann thrombasthenia (GT) lack prophylactic treatment options. As a result, serious bleeding episodes are treated acutely with blood product transfusions or frequent, repeated intravenous administration of recombinant activated coagulation factor VII (rFVIIa). Here we describe HMB-001, a bispecific antibody designed to bind and accumulate endogenous FVIIa and deliver it to sites of vascular injury by targeting it to the TREM (triggering receptor expressed on myeloid cells)-like transcript-1 (TLT-1) receptor that is selectively expressed on activated platelets. In healthy nonhuman primates, HMB-001 prolonged the half-life of endogenous FVIIa, resulting in its accumulation. Mouse bleeding studies confirmed antibody-mediated potentiation of FVIIa hemostatic activity by TLT-1 targeting. In ex vivo models of GT, HMB-001 localized FVIIa on activated platelets and potentiated fibrin-dependent platelet aggregation. Taken together, these results indicate that HMB-001 has the potential to offer subcutaneous prophylactic treatment to prevent bleeds in people with GT and other inherited bleeding disorders, with a low-frequency dosing regimen.
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