This novel combinatorial therapeutic method pairs allogenic stem cell transplantation with an advanced viral vector-mediated gene therapy to boost the crucial GALC enzyme expression. This synergistic approach is designed to overcome the limitations of stem cell transplantation alone, offering therapeutic benefits to both the central and peripheral nervous systems for a more complete treatment of the disease
Description
The innovative therapy targets Krabbe disease, a severe genetic disorder caused by a deficiency in the GALC enzyme, which is essential for normal myelination. The treatment is a synchronized two-part process following initial patient immunosuppression to prepare for cell engraftment. First, allogenic umbilical cord blood (UCB) is administered to establish a donor-derived immune system capable of migrating to the central nervous system (CNS) to produce and deliver the missing enzyme, effectively halting brain degeneration.
This is then immediately followed by the administration of a therapeutic nucleic acid molecule, typically an Adeno-Associated Virus (AAV) vector, designed to express a functional GALC protein. This systemic gene delivery ensures high enzyme expression throughout the body. The combination, which is the key innovation, achieves effective myelination and reduces pathology in the peripheral nervous system (PNS)—a significant clinical challenge untreated by UCB transplant alone—by providing an enhanced supply of the necessary enzyme.
Applications
- Therapeutics for Krabbe disease (globoid cell leukodystrophy), including early infantile, late infantile, and juvenile onset forms.
- Platform technology for combining hematopoietic stem cell transplantation and gene therapy to treat other genetic lysosomal storage disorders.
- Enabling technology for gene therapy, designed to reduce or prevent the immune response (e.g., antibody production) against the viral vector or the newly expressed therapeutic protein.
- Treatment for other genetic disorders in which a therapeutic nucleic acid is needed to express a missing or deficient protein.
- Development of veterinary treatments for naturally-occurring Krabbe disease in other mammals, such as cats and dogs.
Advantages
- Comprehensive Therapeutic Coverage: Successfully treats both the central nervous system (CNS) and the peripheral nervous system (PNS) disease manifestations, overcoming the primary limitation of stem cell therapy alone.
- Increased Survival: Shows potential to significantly increase the survival time of treated patients (demonstrated in animal models).
- Enhanced Neurodevelopmental Outcomes: Aims to increase or improve critical functions, including early learning, motor skills, and other neurodevelopmental milestones.
- Promotes Myelination: Increases myelination in both the CNS and PNS, which is critical for nerve function and repair.
- Reduced Neuropathology: Reduces severe neurological symptoms such as tremors and lowers indicators of inflammation like macrophage infiltration and astrogliosis.
Invention Readiness
This novel combination therapy has demonstrated strong preclinical efficacy and proof-of-concept in the twitcher mouse model of the disease. Data generated from this model shows the combined approach successfully restores normal myelination in the peripheral nervous system, a key area of unmet need, and leads to significantly increased survival compared to either therapy alone. The therapy utilizes a well-characterized viral vector for systemic enzyme delivery. Further studies would focus on final regulatory (IND) submission and transitioning to clinical trials to establish safety, optimal dosing parameters, and therapeutic effect in humans.
IP Status
https://patents.google.com/patent/WO2018136710A1