Neonatal tolerance induction enables accurate evaluation of gene therapy for MPS I in a canine model

- MPS I dogs treated with gene therapy develop immune response against human IDUA.
- MPS I dogs exposed to human IDUA as newborns develop tolerance to the protein.
- Tolerance induction allows for accurate evaluation of human vector in canine model.
- Important approach for preclinical evaluation of gene or protein therapeutics
- Potential to induce tolerance to therapeutic proteins for recessive diseases

High fidelity animal models of human disease are essential for preclinical evaluation of novel gene and protein therapeutics. However, these studies can be complicated by exaggerated immune responses against the human transgene. Here we demonstrate that dogs with a genetic deficiency of the enzyme α-l-iduronidase (IDUA), a model of the lysosomal storage disease mucopolysaccharidosis type I (MPS I), can be rendered immunologically tolerant to human IDUA through neonatal exposure to the enzyme. Using MPS I dogs tolerized to human IDUA as neonates, we evaluated intrathecal delivery of an adeno-associated virus serotype 9 vector expressing human IDUA as a therapy for the central nervous system manifestations of MPS I. These studies established the efficacy of the human vector in the canine model, and allowed for estimation of the minimum effective dose, providing key information for the design of first-in-human trials. This approach can facilitate evaluation of human therapeutics in relevant animal models, and may also have clinical applications for the prevention of immune responses to gene and protein replacement therapies.