An RNAi therapeutic targeting Tmprss6 decreases iron overload in Hfe−/− mice and ameliorates anemia and iron overload in murine β-thalassemia intermedia

• Published in: Blood Vol. 121; no. 7; pp. 1200 - 1208
• Main Authors: Schmidt, Paul J., Toudjarska, Iva, Sendamarai, Anoop K., Racie, Tim, Milstein, Stuart, Bettencourt, Brian R., Hettinger, Julia, Bumcrot, David, Fleming, Mark D.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 14.02.2013; American Society of Hematology
• Subjects: Anemia - genetics; Anemia - metabolism; Anemia - therapy; Animals; Antimicrobial Cationic Peptides - genetics; Antimicrobial Cationic Peptides - metabolism; Base Sequence; beta-Thalassemia - genetics; beta-Thalassemia - metabolism; beta-Thalassemia - therapy; Disease Models, Animal; Erythrocyte Aging; Erythropoiesis; Female; Hemochromatosis - genetics; Hemochromatosis - metabolism; Hemochromatosis - therapy; Hemochromatosis Protein; Hepcidins; Histocompatibility Antigens Class I - genetics; Iron Overload - genetics; Iron Overload - metabolism; Iron Overload - therapy; Membrane Proteins - antagonists & inhibitors; Membrane Proteins - deficiency; Membrane Proteins - genetics; Mice; Mice, Inbred C57BL; Mice, Knockout; Nanoparticles; Red Cells, Iron, and Erythropoiesis; RNA Interference; RNA, Small Interfering - administration & dosage; RNA, Small Interfering - genetics; RNA, Small Interfering - therapeutic use; Serine Endopeptidases - genetics
• ISSN: 0006-4971; 1528-0020
• DOI: 10.1182/blood-2012-09-453977

Mutations in HFE lead to hereditary hemochromatosis (HH) because of inappropriately high iron uptake from the diet resulting from decreased hepatic expression of the iron-regulatory hormone hepcidin. β-thalassemia is a congenital anemia caused by partial or complete loss of β-globin synthesis causing ineffective erythropoiesis, anemia, decreased hepcidin production, and secondary iron overload. Tmprss6 is postulated to regulate hepcidin production by cleaving Hemojuvelin (Hjv), a key modulator of hepcidin expression, from the hepatocyte surface. On this basis, we hypothesized that treatment of mouse models of HH (Hfe−/−) and β-thalassemia intermedia (Hbbth3/+) with Tmprss6 siRNA formulated in lipid nanoparticles (LNPs) that are preferentially taken up by the liver would increase hepcidin expression and lessen the iron loading in both models. In the present study, we demonstrate that LNP-Tmprss6 siRNA treatment of Hfe−/− and Hbbth3/+ mice induces hepcidin and diminishes tissue and serum iron levels. Furthermore, LNP-Tmprss6 siRNA treatment of Hbbth3/+ mice substantially improved the anemia by altering RBC survival and ineffective erythropoiesis. Our results indicate that pharmacologic manipulation of Tmprss6 with RNAi therapeutics isa practical approach to treating iron overload diseases associated with diminished hepcidin expression and may have efficacy in modifying disease-associated morbidities of β-thalassemia intermedia. •Tmprss6 siRNA induces hepcidin and diminishes iron in hemochromatosis or thalassemia mice, improving the anemia seen in the latter model.•Manipulation of TMPRSS6 with RNAi therapeutics may be an approach to treating iron overload diseases associated with low hepcidin levels.