Mies Anna, Hermine Olivier, Platzbecker Uwe
Department of Internal Medicine I, University Hospital Carl Gustav Carus, Technische Universität Dresden, Fetscherstraße 74, 01307, Dresden, Germany.
Department of Hematology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, University Paris Descartes and Imagine Institute, University Sorbonne Paris Cité, 24, boulevard du Montparnasse, 75015, Paris, France.
Curr Hematol Malig Rep. 2016 Dec;11(6):416-424. doi: 10.1007/s11899-016-0347-9.
Distinct subtypes of lower risk myelodysplastic syndromes display ring sideroblasts in the bone marrow, i. e., erythroid progenitors characterized by excessive iron deposited in the mitochondria. This morphological feature is frequently associated with somatic mutations in components of the splicing machinery that constitutes the underlying molecular principle of the disease. Conventional treatment regimen with erythropoiesis-stimulating agents often fails to induce sustained erythroid improvement in these patients that harbor defects in late-stage erythroblasts downstream of erythropoietin action. In the present review, we will discuss activin receptor ligand traps as novel therapeutic strategies particularly for sideroblastic subgroups of myelodysplastic syndromes that were recently shown to alleviate anemia by specifically inhibiting aberrant TGF-β signaling and thereby promoting erythroid differentiation.
低危骨髓增生异常综合征的不同亚型在骨髓中表现出环形铁粒幼红细胞,即红系祖细胞,其特征是线粒体中沉积过多铁。这一形态学特征常与剪接机制成分的体细胞突变相关,而这些突变构成了该疾病的潜在分子原理。对于促红细胞生成素作用下游晚期成红细胞存在缺陷的这些患者,使用促红细胞生成剂的传统治疗方案往往无法诱导持续的红系改善。在本综述中,我们将讨论激活素受体配体陷阱作为新型治疗策略,特别是针对骨髓增生异常综合征的铁粒幼细胞亚组,最近研究表明其可通过特异性抑制异常的转化生长因子-β信号传导从而促进红系分化来缓解贫血。