Effective therapies for type 1 diabetes (T1D) must both restrain immune hyperactivity and reduce β cell susceptibility to destruction. We describe a lipid nanoparticle (LNP) platform for β cell-enriched mRNA delivery that can be further augmented by conjugation to enhanced glucagon-like peptide-1 (eGLP-1). Both unconjugated and eGLP-conjugated LNPs deliver mRNA efficiently to mouse and human β cells in vitro. Biodistribution studies in C57BL/6J mice in vivo demonstrate pancreatic enrichment of LNPs, with greater β cell enrichment achieved by eGLP-LNPs compared with unconjugated LNPs specifically in mice. In prediabetic NOD mice, LNP delivery of PD-L1 mRNA induces β cell PD-L1 expression, attenuates insulitis, and delays the onset of autoimmune diabetes. Importantly, we find that LNPs also deliver mRNA to human β cells in a xenogeneic islet transplantation model in vivo. Together, these findings establish a versatile and translationally relevant LNP platform for β cell-directed mRNA delivery and immune modulation in T1D.
Enriquez et al. (Sun,) studied this question.