The development of more effective gene therapy strategies for hemophilia B remains essential, as results of multiple clinical trials show significant interpatient variability in clinical outcomes, with a fraction of patients (up to 13%) even returning to prophylaxis. Another major challenge in current AAV based gene therapy for hemophilia B pertains to dose-dependent vector-related immune responses, requiring immune suppression. We investigated whether combining gene therapy with transgenes encoding extended half-life (EHL) coagulation factors could enhance therapeutic efficacy. Adeno-associated viral (AAV) vectors encoding a hyperactive factor IX variant R338L (i.e., FIX-Padua), genetically fused to a mutant human albumin (FIX-R338L-ALB(QMP)), were administered to both wild-type and hemophilia B mice. These chimeric transgenes were codon-optimized and driven by a hepatocyte-specific promoter. The AAV-FIX-R338L-ALB(QMP) vector demonstrated significantly improved efficacy compared to the control AAV-FIX-R338L vector, resulting in a sustained 4-fold and 3-fold increase in FIX antigen levels and activity, respectively. These increases were consistent with durable correction of the bleeding phenotype. Importantly, immunogenicity or liver toxicity was not increased, as no anti-FIX antibodies, alanine transaminase elevations, or liver immune infiltrations were detected following treatment. Furthermore, immune tolerance was achieved in the majority of hemophilia B mice treated with AAV-FIX-R338L-ALB(QMP), even after active immunization with FIX protein and adjuvant, which was found to be mediated by regulatory T cells. Additionally, no increase in thrombogenic risk was observed, indicated by stable D-dimer levels. These findings support the potential of FIX-R338L-ALB(QMP) fusion constructs encoding extended half-life FIX as a promising next-generation gene therapy for hemophilia B.
Wolf et al. (Thu,) studied this question.