Year 3 + Wind Down Period
Background: Critical limb ischemia (CLI) represents a significant unmet medical need without any effective medical therapies for patients at high risk of amputation. Currently the only method of treatment for this very severe form of CLI is amputation. Treatment of patients with critical limb ischemia results in a high economic burden to the healthcare system and the individual with the disease, moreover, the mortality (death) of patients undergoing amputation for CLI is very high. Within three months of presentation, 12% of CLI patients will require major amputation, and limb loss rates as high as 30% at 1-2 years have been reported. It is estimated that 160,000 to 180,000 major and minor amputations are performed annually in the United States due to CLI. Fewer than half of all CLI subjects achieve full mobility after an amputation and only one in four above-the-knee amputees will ever wear prosthesis.
Prior and ongoing clinical trials have investigated injection of gene therapy agents for patients with CLI. These therapeutic agents were not significantly better than controls in Phase III trials. Other clinical trials using the patient’s own stem cells, from the bone marrow and injected into the damaged limb are showing some benefit, although the final assessments are not yet completed. Stem cells have shown benefit in treating limb ischemia as they can actively seek out areas of low oxygen and produce some growth factors enabling blood vessel growth. In more severe cases, these strategies alone may not be enough.
Proposed therapy: We have discovered that mesenchymal stem/stromal cells (MSC), a type of adult stem cell, are effective delivery vehicles, moving robustly through the tissue, infusing therapeutic molecules into damaged cells they contact. In mouse models of CLI, injections of MSC into the ischemic area restored blood flow to the limbs. As an improved strategy, we have combined the stem cell and growth factor approaches to make a more potent therapy. We have engineered human MSC from normal donor bone marrow to produce high levels of the angiogenic agent VEGF (MSC/VEGF). It is well documented that MSC are capable of sustained expression of growth factors, migrate to areas of lowest oxygen in the tissues after injection, and wrap around the damaged or tiny blood vessels to secrete factors where they are needed most to restore blood flow. We propose to use these MSC as “nature’s own paramedic system”, arming them with VEGF to enhance collateral blood vessel growth.
Progress, Year 3 of grant: We have successfully engineered human MSCs to produce VEGF with the pivotal vector and performed additional efficacy and safety studies.
We have shown that MSC/VEGF produces high levels of VEGF with bioactivity, and that a multiplicity of infection of one virus particle per cell generates a single unrearranged integrant per cell, on average. This data is critical to the Recombinant DNA Advisory Committee (RAC), for whom we submitted an Appendix M application and received RAC approval to proceed to the FDA with the preIND submission for the proposed stem cell gene therapy trial.
We shared this information and our pivotal VEGF vector with our collaborative funding partners (CFP) at Hospital Reina Sofia in Cordoba, Andalucía, Spain. Personnel from both groups have visited each other’s facilities and we continue to have regular meetings to ensure we are collectively moving forward. We shared our RAC document with our CFP which includes the proposed clinical protocol. We plan to follow similar procedures, with the exception being the route of administration of MSC/VEGF into patients: intramuscular injection at UCD and intra-arterial in Spain. The clinical trials in both California and Spain will enable us to compare results from the same cellular product, strengthening our conclusions.
We have successfully completed four efficacy experiments; the MSC/VEGF cell product caused significantly increased blood flow in the ischemic limb, as compared to the saline controls in each study. In addition we have performed safety studies including the following: measuring secreted VEGF levels, karyotypic stability, examining genetic stability, performing rule-out tumorigenicity assays, conducting rule-out hemangioma and edema assays, pericyte study, and retention.