Endothelial siRNA delivery in nonhuman primates using ionizable low–molecular weight polymeric nanoparticles

Omar F. Khan, Piotr S. Kowalski, Joshua C. Doloff, Jonathan K. Tsosie, Vasudevan Bakthavatchalu, Caroline Bodi Winn, Jennifer Haupt, Morgan Jamiel, Robert Langer, Daniel G. Anderson

Research output: Contribution to journalArticlepeer-review

Abstract

Dysfunctional endothelial cells contribute to the pathophysiology of many diseases, including vascular disease, stroke, hypertension, atherosclerosis, organ failure, diabetes, retinopathy, and cancer. Toward the goal of creating a new RNA-based therapy to correct aberrant endothelial cell gene expression in humans, efficient gene silencing in the endothelium of nonhuman primates was achieved by delivering small interfering RNA (siRNA) with 7C1, a low–molecular weight, ionizable polymer that forms nanoparticles. After a single intravenous administration of 1 mg of siRNA per kilogram of animal, 7C1 nanoparticles delivering Tie2 siRNA caused Tie2 mRNA levels to decrease by approximately 80% in the endothelium of the lung. Significant decreases in Tie2 mRNA were also found in the heart, retina, kidney, pancreas, and bone. Blood chemistry and liver function analysis before and after treatment all showed protein and enzyme concentrations within the normal reference ranges. Furthermore, after controlling for siRNA-specific effects, no significant increases in inflammatory cytokine concentrations were found in the serum. Similarly, no gross lesions or significant underlying pathologies were observed after histological examination of nonhuman primate tissues. This study is the first demonstration of endothelial gene silencing in multiple nonhuman primate organs using systemically administered siRNA nanoparticles and highlights the potential of this approach for the treatment of disease in humans.

Original languageEnglish (US)
Article numbereaar8409
JournalScience Advances
Volume4
Issue number6
DOIs
StatePublished - Jun 27 2018

ASJC Scopus subject areas

  • General

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