Ineffective erythropoiesis and regulation of iron status in iron loading anaemias

被引:128
作者
Camaschella, Clara [1 ]
Nai, Antonella [1 ]
机构
[1] Univ Vita Salute San Raffaele, Div Genet & Cell Biol, San Raffaele Sci Inst, Milan, Italy
关键词
anaemia; iron; iron overload; erythropoiesis; thalassaemia; DIFFERENTIATION FACTOR 15; BETA-THALASSEMIA; MOUSE MODEL; MYELODYSPLASTIC SYNDROME; TRANSFERRIN RECEPTOR; HEPCIDIN EXPRESSION; ERYTHROID REGULATOR; AMELIORATES ANEMIA; SKELETAL-MUSCLE; SERUM FERRITIN;
D O I
10.1111/bjh.13820
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The definition iron loading anaemias' encompasses a group of inherited and acquired anaemias characterized by ineffective erythropoiesis, low hepcidin levels, excessive iron absorption and secondary iron overload. Non-transfusion-dependent -thalassaemia is the paradigmatic example of these conditions that include dyserythropoietic and sideroblastic anaemias and some forms of myelodysplasia. Interrupting the vicious cycle between ineffective erythropoiesis and iron overload may be of therapeutic benefit in all these diseases. Induction of iron restriction by means of transferrin infusions, minihepcidins or manipulation of the hepcidin pathway prevents iron overload, redistributes iron from parenchymal cells to macrophage stores and partially controls anaemia in -thalassaemic mice. Inhibition of ineffective erythropoiesis by activin ligand traps improves anaemia and iron overload in the same models. Targeting iron loading orineffective erythropoiesis shows promise in preclinical studies; activin ligand traps are in clinical trials with promising results and may be useful in patients with ineffective erythropoiesis.
引用
收藏
页码:512 / 523
页数:12
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