The efficacy and the risk of immunogenicity of FIX Padua (R338L) in hemophilia B dogs treated by AAV muscle gene therapy

Introduction

Hemophilia B (HB) is an X-linked bleeding disorder resulting from a deficiency of coagulation factor IX (FIX). Gene therapy is an attractive strategy for the treatment of the disease because continuous maintenance of FIX levels as low as 1%-5% of normal have been shown to substantially ameliorate the bleeding phenotype in both preclinical and clinical models.^1–6

Studies using adeno-associated viral (AAV) vectors showed that the safety profile is vector dose-dependent.^3,4 In a liver-directed approach, immune responses to AAV-capsid proteins at the highest dose tested (2 × 10¹² vg/kg) required transient immunosuppression for sustained transgene expression.^3,4 In a study on direct intramuscular AAV-FIX, the safety profile was excellent² and the local transgene expression of FIX in the injected muscle persisted for 3.7 and 10 years in 2 human subjects tested.^7,8 However, all doses tested in the intramuscular study resulted in subtherapeutic circulating FIX levels.² The use of FIX variants with gain of function offers the opportunity to enhance the efficacy of gene-based approaches for HB without increasing the vector doses. In an early study, we demonstrated that replacement of arginine 338 by alanine (R338A) was associated with an ∼ 3-fold increase in the protein specific activity in murine models of HB receiving AAV-FIX-R338A⁹ as later confirmed in other models.^10,11 Recently, we described a naturally occurring gain-of-function mutation in humans characterized by leucine at position 338 (R338L), which exhibits normal antigen levels, but an ∼ 8-fold higher specific activity.¹² Notably, the arginine at position 338 in FIX is conserved among mammals, and this region of the enzyme appears to be part of the substrate exosite for factor X.¹³ Here we report, for the first time, the use of the homologous FIX-R338L in a large and immunocompetent canine model of severe HB (< 1% of normal).

Methods

Results and discussion

Skeletal muscle is an ideal target for the expression of therapeutic transgenes in genetic diseases that are associated with primary or iatrogenic underlying liver disease. In adults with hemophilia, the high rates of viral hepatitis resulting from blood transfusion preclude the enrollment of many patients in liver-directed gene therapy. We sought to test whether cFIX-R338L could be safely expressed in HB dogs by regional transvenular delivery of AAV vector to skeletal muscle of a single limb. We generated an AAV-6 vector encoding cFIX-338L and delivered it to 3 adult HB dogs. We chose to use an AAV-6 vector given the excellent tropism for systemic transduction of striated muscle¹⁵ and our own experience using AAV-6 for muscle transduction in HB dogs.¹ There was a continuous increase in the circulating cFIX levels that reached plateau levels after day 100 (Figure 1). The kinetics and magnitude of expression in cFIX-338L dogs were similar to those observed in our earlier studies in dogs using cFIX wild-type (WT) via transvenular route.¹ In a series of previous studies in HB dogs after liver, intramuscular, or intravascular delivery to skeletal muscle of AAV vectors of distinct serotypes expressing cFIX-WT, there was a linear correlation between cFIX antigen and activity levels (ration, 0.8-1.1).^1,3,5,16 Here the ratio of antigen and activity clearly demonstrated that cFIX-338L exhibits an 8- to 9-fold higher specific activity of the protein (Table 1), as observed in humans with R338L.¹² The expression of cFIX-338L was accompanied by normalization of the whole blood clotting time 1 week after vector delivery; this was stable throughout the follow-up (Table 1) and comparable with values observed in hemostatically normal dogs.¹⁷ Moreover, no spontaneous bleeding episodes requiring treatment occurred for a cumulative period of ∼ 5 years after vector delivery (ongoing observations). The frequency of spontaneous bleeding episodes in untreated HB dogs is 5.5 bleeds per dog/year¹⁸; thus, the phenotypic improvement supported by cFIX-338L is clinically evident.

One important consideration in any novel therapeutic approach for hemophilia is the risk of induction of neutralizing antibodies to the clotting factor. The success of gene therapy strategies to cure disease relies on the control of unwanted immune responses to transgene products, genetically modified cells, and/or to the vector.¹⁹ In early studies, we showed that transient immunosuppression (up to 4 weeks) of postskeletal muscle delivery of AAV-cFIX is required to prevent antibodies to the cFIX-WT transgene.^1,6,19 One potential risk of introducing FIX with a variant sequence distinct from the WT protein is the immune response to the neotransgene product. The underlying mutation in the HB model from the University of North Carolina is a missense mutation that results in a G379E substitution in cFIX.²⁰ Notably, there was no formation of inhibitory antibodies to cFIX-R338L on multiple challenges with cFIX-WT protein, even > 1 year after stopping immunosuppression (Figure 1B-C). These data were further supported by the lack of IFN-γ secretion by T cells after exposure to FIX-WT protein, peptides spanning the 338 residue with (R or L), and AAV-6 capsid (Figure 1D). Thus, the FIX-R338L variant shows no detectable immunogenicity in this approach. There was also no evidence of local or systemic toxicity, changes in TAT levels (data not shown), or clinically evident thrombotic complications; however, these data should be interpreted cautiously given the small number of animals used in this study. The latter is consistent with limited observation in humans where only patients with supraphysiologic levels of FIX-R338L (> 700% of normal) developed thrombosis¹² (and P.S., unpublished data, August 2011).

The expression of FIX-R338L variant has the potential to lower the therapeutic vector dose and is an attractive strategy to overcome limitations in performing critical posttranslational modifications for a fully biologically active transgene in ectopic targets⁶ as we previously reported in murine models of HB.⁹ Moreover, the superior specific activity of FIX-R338L was also exhibited after infusion of recombinant FIX-R338L in HB dogs (V.R.A., unpublished data, January 2012). In conclusion, our findings in HB dogs support the use of FIX-338L for clinical translational studies of HB in a variety of therapeutic settings, such as protein replacement or gene-based approaches targeting the liver or ectopic sites.

Authorship

Contribution: J.D.F. designed and executed the experiments and drafted the manuscript; T.C.N., E.P.M., and D.A.B. performed the vector administration, provided care to the animals, and collected laboratory samples; N.S. executed the T-cell assays; S.Z. provided the recombinant AAV vectors used in this study; P.S. and K.A.H. provided insights on experimental design and edited the manuscript; and V.R.A. directed experimental design, conducted data analysis and interpretation, and drafted the manuscript.

Conflict-of-interest disclosure: K.A.H. holds patents related to AAV manufacture and purification. She holds patents related to AAV-FIX, in which she has waived any financial interest. The remaining authors declare no competing financial interests.

Correspondence: Valder R. Arruda, Children's Hospital of Philadelphia, 3501 Civic Center Blvd, 5056 Colket Translational Research Center, Philadelphia, PA 19104; e-mail: arruda@e-mail.chop.edu.