MG53: Enhancing Tissue Performance and Repairing Damaged Tissue, T2019-164, T2020-002, T2020-159, T2020-222: Using rhMG53 to treat conditions involving damaged tissue, including corneal repair, hepatic tissue injury, inflammatory bowel disease, and other tissue injury. The Need While MG53 is naturally present in skeletal and cardiac muscle, its levels are often insufficient to optimize tissue performance. Current treatments leveraging exogenous MG53 are therapeutically ineffective for conditions like multiple sclerosis, viral infections, radiation-induced tissue injury, and obesity. There is a critical need for innovative methods to enhance the functionality of otherwise healthy tissues, including skeletal muscle, cardiac muscle, kidney, neuronal, and corneal tissues, beyond just repair. The Technology Researchers at The Ohio State University have developed a therapeutic approach to enhancing performance of a variety of tissues by systemically administering recombinant human MG53 (rhMG53). The technology encompasses a variety of dosage forms, including biological and non-biological carriers, that either directly deliver MG53 to the target tissue or enable its expression within the target tissues. By leveraging viral vectors, autologous blood serum, and bioengineered hematopoietic stem cells, this method ensures efficient and targeted delivery of MG53, thereby significantly improving tissue function. Commercial Applications
Benefits/Advantages
Patent Applications Pending in US and Multiple Countries |
Tech IDT2020-129 CollegeLicensing ManagerSchultz, Teri InventorsCategories |