Tumor Homing Nanoparticle Immunotherapy for Acute Clearance and Mitigation of T-cell Exhaustion in Humanized High-Risk Neuroblastoma
Authors:
- Griffin I. KaneGKGriffin I. Kane
- Miranda B. Diaz-InfanteMDMiranda B. Diaz-Infante
- Kim WigglesworthKWKim Wigglesworth
- Ellis LusiELEllis Lusi
- Meghan BrassilMBMeghan Brassil
- Esteban J. RozenEREsteban J. Rozen
- Jamie KadyJKJamie Kady
- Haruka MoriHMHaruka Mori
- John LukasJLJohn Lukas
- Tiana NaylorTNTiana Naylor
- Ronnie W. DinnellRDRonnie W. Dinnell
- Katherine C. MurphyKMKatherine C. Murphy
- 26 March 2026
- journal article
- Published by American Association for Cancer Research (AACR) in Molecular Cancer Therapeutics
- p. OF1-OF13
Abstract
Effective treatments for high-risk neuroblastoma, a pediatric malignancy with dismal survival outcomes, demand strategies that remodel the “cold” immunosuppressive tumor microenvironment (TME) to “hot” and proinflammatory. In this study, we interrogate the mechanistic efficacy of a pathogen-inspired nanoparticle (NP) technology that leverages the advantages of lipids to co-deliver a combination of physically distinct but functionally synergistic innate immune agonists for dual pathway activation in humanized mouse models. Specifically, our immunomodulatory NPs (immuno-NPs) co-deliver agonists of the stimulator of interferon (IFN) genes and Toll-like receptor 4 pathways. Together, dual pathway activation in target cells in the TME by immuno-NPs promotes the synergistic production of type I IFNs and other proinflammatory cytokines that powerfully remodel the cytokine milieu. We show that immuno-NPs can be delivered safely in the systemic blood circulation for deposition in the perivascular space of neuroblastoma primary tumors and metastases. Their broad uptake across immune cells, endothelial cells, and even tumor cells drives significant immune activation and restructuring of the cytokine milieu of the TME. We also demonstrate a pivotal role for otherwise exhausted CD8+ T cells that are local and already infiltrating the tumor. Immuno-NP–mediated rescue of this local T-cell subset is chiefly responsible for the acute clearance responses that may be essential for treatment efficacy in aggressive cancers like high-risk neuroblastoma. Taken together, our findings make a strong case for the use of pathogen-inspired, multi-innate pathway-activating therapies, such as immuno-NPs, for high-risk neuroblastoma and other solid tumor malignancies that urgently warrant effective TME remodeling approaches.Keywords
All Related Versions
Funding Information
- Alex's Lemonade Stand Foundation for Childhood Cancer
- National Cancer Institute (K22CA262355)
- National Institute of Biomedical Imaging and Bioengineering (R21EB034465)
- Institute for Applied Life Sciences, University of Massachusetts Amherst
- National Science Foundation Graduate Research Fellowship Program
- Alex's Lemonade Stand Foundation for Childhood Cancer
This publication has 49 references indexed in Scilit:
- Innate cell communication kick-starts pathogen-specific immunityNature Immunology, 2016
- Nano-Therapeutics for the Lung: State-of-the-Art and Future PerspectivesCurrent Pharmaceutical Design, 2015
- Mechanisms and pathways of innate immune activation and regulation in health and cancerHuman Vaccines & Immunotherapeutics, 2014
- IL-26 is overexpressed in chronically HCV-infected patients and enhances TRAIL-mediated cytotoxicity and interferon production by human NK cellsGut, 2014
- Type I interferons up-regulate the expression and signalling of p75 NTR/TrkA receptor complex in differentiated human SH-SY5Y neuroblastoma cellsNeuropharmacology, 2014
- Type I interferons impair BDNF‐induced cell signaling and neurotrophic activity in differentiated human SH‐SY5Y neuroblastoma cells and mouse primary cortical neuronsJournal of Neurochemistry, 2012
- Innate immunity in the human lung: pathogen recognition and lung diseaseCell and tissue research, 2010
- Parameters for establishing humanized mouse models to study human immunity: Analysis of human hematopoietic stem cell engraftment in three immunodeficient strains of mice bearing the IL2rγnull mutationClinical Immunology, 2010
- PolyI:C plus IL‐2 or IL‐12 induce IFN‐γ production by human NK cells via autocrine IFN‐βEuropean Journal of Immunology, 2009
- Innate and adaptive immunity: specificities and signaling hierarchies revisitedNature Immunology, 2004