Abstract 4374: A novel RNA-LNP immunotherapy platform to drive anti-tumor efficacy in solid tumors

Abstract Nucleoside-modified RNA vaccines complexed in ionizable lipid nanoparticles (RNA-LNPs) constitute a promising immunotherapy platform for T cell-directed cancer vaccine development. A challenge in generating a proper anti-tumor CD8 T cell response with current RNA vaccine iterations remains, however, in providing optimal activation of antigen-presenting cells. Further, the presence of an immunologically cold tumor microenvironment (TME) presents an additional obstacle in designing an immunotherapeutic strategy to overcome such immunosuppression. To address these challenges, we hypothesized that an optimized RNA-LNP platform which couples an antigen-encoding RNA with a novel RNA-LNP innate immune activator will synergistically activate dendritic cells (DCs) by engaging multiple pattern recognition receptor (PRR) pathways to enhance cross-presentation and drive CD8 T cell responses. To this end, we immunized mice with our novel RNA-LNP platform and demonstrated that multiple DC subsets were activated at both local and distal secondary lymphoid organs respective to the injection site. The DCs from the immunized mice also activated and expanded antigen-specific T cells and resulted in memory T cell formation. Abrogation of these T cell responses in genetic knockout models demonstrate that such T cell activation is mediated by multiple PRRs. Systemic delivery of the novel innate immune activators activated DCs at draining lymph nodes local to the tumor site in an orthotopically implanted murine pancreatic cancer model and subsequently conferred tumor growth suppression. Collectively, these studies establish a new paradigm for RNA-LNP immunotherapy that integrates multifaceted PRR engagement to promote antigen-specific vaccination and facilitate T cell priming and reactivation at the tumor. Citation Format: Hailey R. Lee, Khalid Rashid, Tony Luu, Amanda Creech, Pu-Lin Teng, Emma Lieberman, Bridget Vause, Catherine Xie, Britney Trieu, Willy Hugo, Ting-Ting Wu, Norbert Pardi, Caius G. Radu. A novel RNA-LNP immunotherapy platform to drive anti-tumor efficacy in solid tumors [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4374.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-4374
Primary Topic
RNA Interference and Gene Delivery
Type
article
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article

Abstract 4374: A novel RNA-LNP immunotherapy platform to drive anti-tumor efficacy in solid tumors

Amanda L. Creech, Caius G. Radu, Willy Hugo, Khalid Rashid et al.
Cancer Research
RNA Interference and Gene Delivery
article

Abstract 4374: A novel RNA-LNP immunotherapy platform to drive anti-tumor efficacy in solid tumors

Amanda L. Creech, Caius G. Radu, Willy Hugo, Khalid Rashid, Tony Luu, Hailey R. Lee, Emma Lieberman, Pu-Lin Teng, Bridget Vause, Norbert Pardi, Ting-Ting Wu, Britney Trieu, Catherine Xie
article en

Abstract

Abstract Nucleoside-modified RNA vaccines complexed in ionizable lipid nanoparticles (RNA-LNPs) constitute a promising immunotherapy platform for T cell-directed cancer vaccine development. A challenge in generating a proper anti-tumor CD8 T cell response with current RNA vaccine iterations remains, however, in providing optimal activation of antigen-presenting cells. Further, the presence of an immunologically cold tumor microenvironment (TME) presents an additional obstacle in designing an immunotherapeutic strategy to overcome such immunosuppression. To address these challenges, we hypothesized that an optimized RNA-LNP platform which couples an antigen-encoding RNA with a novel RNA-LNP innate immune activator will synergistically activate dendritic cells (DCs) by engaging multiple pattern recognition receptor (PRR) pathways to enhance cross-presentation and drive CD8 T cell responses. To this end, we immunized mice with our novel RNA-LNP platform and demonstrated that multiple DC subsets were activated at both local and distal secondary lymphoid organs respective to the injection site. The DCs from the immunized mice also activated and expanded antigen-specific T cells and resulted in memory T cell formation. Abrogation of these T cell responses in genetic knockout models demonstrate that such T cell activation is mediated by multiple PRRs. Systemic delivery of the novel innate immune activators activated DCs at draining lymph nodes local to the tumor site in an orthotopically implanted murine pancreatic cancer model and subsequently conferred tumor growth suppression. Collectively, these studies establish a new paradigm for RNA-LNP immunotherapy that integrates multifaceted PRR engagement to promote antigen-specific vaccination and facilitate T cell priming and reactivation at the tumor. Citation Format: Hailey R. Lee, Khalid Rashid, Tony Luu, Amanda Creech, Pu-Lin Teng, Emma Lieberman, Bridget Vause, Catherine Xie, Britney Trieu, Willy Hugo, Ting-Ting Wu, Norbert Pardi, Caius G. Radu. A novel RNA-LNP immunotherapy platform to drive anti-tumor efficacy in solid tumors [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4374.

Cancer ResearchVol. 86(7_Supplement)
APLA Health (US), UCLA Health (US), University of Pennsylvania (US)
Good health and well-being
Openalex Percentile: Top 32%
RNA Interference and Gene Delivery
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