A novel RNA therapeutic utilizing lipid nanoparticles for precision inhibition of SPP1 in tumor-associated myeloid cells, aiming to reprogram these cells and boost anti-tumor immunity by enhancing T cell infiltration and activation.
This innovative RNA therapeutic is designed to precisely target and inhibit Secreted Phosphoprotein 1 (SPP1) within tumor-associated myeloid cells (TAMCs), such as tumor-associated macrophages (TAMs) and myeloid-derived suppressor cells (MDSCs). By employing lipid nanoparticle-based delivery, the therapy aims to reprogram these immunosuppressive cells, enhancing their ability to present antigens and elicit a robust anti-tumor response. The approach has shown promise in increasing the phagocytosis of tumor cells and promoting T cell activation and infiltration, which are crucial for effective tumor killing.
Currently, the technology is at TRL 4, having been validated in a laboratory setting. Further validation is planned using animal models to assess the therapeutic's impact on TAMC functionality, T cell behavior, and overall anti-tumor efficacy. Additional studies will explore the reshaping of the tumor microenvironment, with the goal of advancing to higher readiness levels.
Northwestern University is a comprehensive private research university with campuses in Evanston and downtown Chicago and a collaborative, cross‑disciplinary culture. Integration with a major hospital system enables clinical research, diverse patient access, and rapid translation from bench to bedside. Shared research cores, prototyping facilities, a campus incubator, and dedicated corporate engagement teams make it straightforward to scope projects, structure agreements, and place talent. Research is supported by competitive federal funding from agencies such as NIH, NSF, DOE, and DoD, complemented by foundation and industry partnerships. A dedicated technology transfer office advances IP strategy, licensing, and startup formation.