Drug intelligence / Profile preview

interleukin-2-conjugated lipid nanoparticles

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

Overview

Interleukin-2-conjugated lipid nanoparticles (IL2-LNPs) are an investigational targeted mRNA delivery platform designed for in vivo regulatory T cell (Treg) immunotherapy. Developed by researchers at the University of Pennsylvania, these lipid nanoparticles are surface-conjugated with interleukin-2 (IL-2) using a SATA-maleimide-based strategy. This conjugation exploits the constitutively high expression of the high-affinity IL-2 receptor (specifically CD25) on Tregs to facilitate selective uptake of the mRNA-LNP cargo. In preclinical models, IL2-LNPs have demonstrated highly selective and efficient delivery of mRNA to Tregs in the spleen, lymph nodes, and blood, with minimal background uptake by other immune cell subsets. This platform is being investigated for its potential to transiently enhance or alter Treg function in situ for the treatment of autoimmune diseases, such as type 1 diabetes.

Other names
IL-2-LNPIL2-LNPIL 2-LNPIL-2-LNPsIL2-LNPsIL 2-LNPsIL-2-conjugated lipid nanoparticlesIL2-conjugated lipid nanoparticlesIL 2-conjugated lipid nanoparticlesinterleukin-2-conjugated mRNA-lipid nanoparticlesinterleukin2-conjugated mRNA-lipid nanoparticlesinterleukin 2-conjugated mRNA-lipid nanoparticles
02

Targets

IL2RG (Interleukin-2 receptor gamma subunit)IL2RA (Interleukin-2 receptor alpha subunit)IL2RB (IL-2 receptor beta chain)

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