Modified activin receptor IIB ligand trap mitigates ineffective erythropoiesis and disease complications in murine β-thalassemia

RNVS Suragani, SM Cawley, R Li… - Blood, The Journal …, 2014 - ashpublications.org
RNVS Suragani, SM Cawley, R Li, S Wallner, MJ Alexander, AW Mulivor, S Gardenghi…
Blood, The Journal of the American Society of Hematology, 2014ashpublications.org
In β-thalassemia, unequal production of α-and β-globin chains in erythroid precursors
causes apoptosis and inhibition of late-stage erythroid differentiation, leading to anemia,
ineffective erythropoiesis (IE), and dysregulated iron homeostasis. Here we used a murine
model of β-thalassemia intermedia (Hbb th1/th1 mice) to investigate effects of a modified
activin receptor type IIB (ActRIIB) ligand trap (RAP-536) that inhibits Smad2/3 signaling. In
Hbb th1/th1 mice, treatment with RAP-536 reduced overactivation of Smad2/3 in splenic …
Abstract
In β-thalassemia, unequal production of α- and β-globin chains in erythroid precursors causes apoptosis and inhibition of late-stage erythroid differentiation, leading to anemia, ineffective erythropoiesis (IE), and dysregulated iron homeostasis. Here we used a murine model of β-thalassemia intermedia (Hbbth1/th1 mice) to investigate effects of a modified activin receptor type IIB (ActRIIB) ligand trap (RAP-536) that inhibits Smad2/3 signaling. In Hbbth1/th1 mice, treatment with RAP-536 reduced overactivation of Smad2/3 in splenic erythroid precursors. In addition, treatment of Hbbth1/th1 mice with RAP-536 reduced α-globin aggregates in peripheral red cells, decreased the elevated reactive oxygen species present in erythroid precursors and peripheral red cells, and alleviated anemia by promoting differentiation of late-stage erythroid precursors and reducing hemolysis. Notably, RAP-536 treatment mitigated disease complications of IE, including iron overload, splenomegaly, and bone pathology, while reducing erythropoietin levels, improving erythrocyte morphology, and extending erythrocyte life span. These results implicate signaling by the transforming growth factor-β superfamily in late-stage erythropoiesis and reveal potential of a modified ActRIIB ligand trap as a novel therapeutic agent for thalassemia syndrome and other red cell disorders characterized by IE.
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