Abstract B83: RNA-nanoparticles for immunotherapy-resistant head and neck squamous cell carcinoma

• Published in: Cancer immunology research 2020-04, Vol.8 (4_Supplement), p.B83-B83
• Main Authors: Silver, Natalie L., Garg, Rekha R., Fredenberg, Kristianna M., Mendez, Hector R., Mitchell, Duane A., Sayour, Elias J.
• Format: Article
• Language: English
• ISSN: 2326-6066; 2326-6074
• DOI: 10.1158/2326-6074.TUMIMM18-B83

Introduction: Immunotherapy is promising for patients with treatment-refractory head and neck squamous cell carcinoma (HNSCC). However, >80% of patients do not respond to checkpoint inhibitors, suggesting that the highly immunosuppressive tumor immune microenvironment of HNSCC may play a role in treatment resistance. Our group has developed a novel treatment platform utilizing clinically translatable RNA-nanoparticles (NPs) to remodel the systemic and intratumoral HNSCC microenvironment in favor of an activated immunologic milieu. Objective: The purpose of this study is to examine the feasibility, safety and immunologic activity of systemic/intratumoral administration of RNA NPs for HNSCC. Materials and Methods: RNA-NPs were prepared by complexing negatively charged mRNA with nanoliposomes. These complexes were injected into naive and B16 or MOC1/MOC2 (murine oral cavity squamous cell carcinoma cell lines) tumor bearing C57Bl/6 mice. In vitro transfection experiments were performed in human HNSCC cell lines. Results: Human HNSCC cell lines were efficiently transfected with RNA NPs in vitro. MOC1/MOC2 tumors were efficiently transfected with RNA NPs in vivo. RNA-NPs activate dendritic cells (DCs) in the peripheral and intratumoral microenviroment of naive and B16 tumor bearing mice, and mediate antitumor efficacy in a preclinical in vivo murine model for HNSCC. RNA-NPs mediate their effects through interferon-alpha released from plasmacytoid DCs. We have successfully scaled up production of RNA-NPs for translation into human clinical trials and demonstrated safety of RNA-NPs in acute/chronic murine toxicity studies based on CBCs, electrolytes, organ function tests, and end-organ H&E histology. Conclusions: RNA-NPs safely reprogram the peripheral and intratumoral immune microenvironments, unlocking antitumor activity. We have successfully generated RNA-NPs, providing a renewable resource that can be made readily available for all HNSCC patients. FDA-IND enabling studies are currently under way in preparation for first-in-human trials for checkpoint refractory HNSCC. Citation Format: Natalie L. Silver, Rekha R. Garg, Kristianna M. Fredenberg, Hector R. Mendez, Duane A. Mitchell, Elias J. Sayour. RNA-nanoparticles for immunotherapy-resistant head and neck squamous cell carcinoma [abstract]. In: Proceedings of the AACR Special Conference on Tumor Immunology and Immunotherapy; 2018 Nov 27-30; Miami Beach, FL. Philadelphia (PA): AACR; Cancer Immunol Res 2020;8(4