Infused factor VIII–expressing platelets or megakaryocytes as a novel therapeutic strategy for hemophilia A

• Published in: Blood advances 2019-05, Vol.3 (9), p.1368-1378
• Main Authors: Lyde, Randolph B., Ahn, Hyun Sook, Vo, Karen K., Jarocha, Danuta J., Tkaczynski, John, Treffeisen, Elsa, Sullivan, Spencer K., Camire, Rodney M., Sabatino, Denise E., French, Deborah L., Poncz, Mortimer
• Format: Article
• Language: English
• Subjects: Animals; Area Under Curve; Blood Platelets - cytology; Blood Platelets - metabolism; Factor VIIa - therapeutic use; Factor VIII - analysis; Factor VIII - genetics; Factor VIII - metabolism; Hemophilia A - mortality; Hemophilia A - therapy; Humans; Male; Megakaryocytes - cytology; Megakaryocytes - metabolism; Megakaryocytes - transplantation; Mice; Mice, Inbred C57BL; Mice, Transgenic; Platelet Transfusion; ROC Curve; Survival Rate; Thrombosis and Hemostasis; Treatment Outcome
• ISSN: 2473-9529; 2473-9537
• DOI: 10.1182/bloodadvances.2017007914

B-domainless factor VIII (FVIII) ectopically expressed in megakaryocytes (MKs) is stored in α granules of platelets (pFVIII) and is capable of restoring hemostasis in FVIIInull mice, even in the presence of circulating inhibitors. However, our prior studies have shown that this ectopically expressed pFVIII can injure developing MKs. Moreover, the known risks of prolonged thrombocytopenia after bone marrow transplantation are significant challenges to the use of this strategy to treat individuals with severe hemophilia A and particularly those with intractable clinically relevant inhibitors. Because of these limitations, we now propose the alternative therapeutic pFVIII strategy of infusing pFVIII-expressing MKs or platelets derived from induced pluripotent stem cells (iPSCs). pFVIII-expressing iPSC-derived MKs, termed iMKs, release platelets that can contribute to improved hemostasis in problematic inhibitor patients with hemophilia A. As proof of principle, we demonstrate that hemostasis can be achieved in vitro and in vivo with pFVIII-expressing platelets and show prolonged efficacy. Notably, pFVIII-expressing platelets are also effective in the presence of inhibitors, and their effect was enhanced with recombinant FVIIa. Human pFVIII-expressing iMKs improved hemostasis in vitro, and derived platelets from infused human pFVIII-expressing iMKs improved hemostasis in FVIIInull mice. These studies indicate the potential therapeutic use of recurrent pFVIII-expressing MK or platelet infusions with prolonged hemostatic coverage that may be additive with bypassing agents in hemophilia A patients with neutralizing inhibitors. •Recurrent infused iPSC-derived MKs or platelets expressing FVIII are an effective hemostatic strategy for hemophilia A.•Platelets expressing FVIII are additive with recombinant activated FVII in the setting of hemophilia A. [Display omitted]