Drug intelligence / Profile preview

mRNA-loaded apolipoprotein A1 nanoparticles

Development stage
Preclinical
Lead developer
Biotrip
Modality
mRNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

mRNA-loaded apolipoprotein A1 nanoparticles (aNPs) are a nature-inspired delivery platform designed to transport messenger RNA (mRNA) to immune cells within secondary lymphoid organs, such as the spleen and lymph nodes. Developed by Biotrip in collaboration with the Eindhoven University of Technology and Radboud University Medical Center, these nanoparticles utilize a combination of apolipoprotein A1 and proprietary dendrimer-based ionizable lipids (e.g., HMJ1, HMJ2) to encapsulate mRNA. The primary therapeutic strategy involves delivering mRNA encoding cytokines, such as human interleukin-2 (hIL-2) or interferon-gamma (IFN-gamma), to stimulate local immune responses and activate CD8+ T cells for cancer immunotherapy. This approach aims to achieve robust immunomodulation while minimizing the systemic toxicity often associated with traditional cytokine treatments. Preclinical studies in mouse models of melanoma and colorectal cancer have demonstrated significant tumor growth inhibition and improved survival, with additional validation performed in non-human primates and patient-derived monocytes.

Other names
apolipoprotein A1 nanoparticlesaNP platform
02

Targets

IL-2R (Interleukin-2/interleukin-15 receptor complex)IFNGR1 (Interferon gamma receptor 1)CD8A (T-cell surface glycoprotein CD8 alpha chain)

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