Langdon Jacqueline M, Barkataki Sangjucta, Berger Alan E, Cheadle Chris, Xue Qian-Li, Sung Victoria, Roy Cindy N
Division of Geriatric Medicine and Gerontology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Am J Hematol. 2015 Jan;90(1):8-14. doi: 10.1002/ajh.23856. Epub 2014 Oct 25.
Over expression of hepcidin antimicrobial peptide is a common feature of iron-restricted anemia in humans. We investigated the erythroid response to either erythropoietin or RAP-011, a "murinized" ortholog of sotatercept, in C57BL/6 mice and in hepcidin antimicrobial peptide 1 over expressing mice. Sotatercept, a soluble, activin receptor type IIA ligand trap, is currently being evaluated for the treatment of anemias associated with chronic renal disease, myelodysplastic syndrome, β-thalassemia, and Diamond Blackfan anemia and acts by inhibiting signaling downstream of activin and other Transforming Growth Factor-β superfamily members. We found that erythropoietin and RAP-011 increased hemoglobin concentration in C57BL/6 mice and in hepcidin antimicrobial peptide 1 over expressing mice. While erythropoietin treatment depleted splenic iron stores in C57BL/6 mice, RAP-011 treatment did not deplete splenic iron stores in mice of either genotype. Bone marrow erythroid progenitors from erythropoietin-treated mice exhibited iron-restricted erythropoiesis, as indicated by increased median fluorescence intensity of transferrin receptor immunostaining by flow cytometry. In contrast, RAP-011-treated mice did not exhibit the same degree of iron-restricted erythropoiesis. In conclusion, we have demonstrated that RAP-011 can improve hemoglobin concentration in hepcidin antimicrobial peptide 1 transgenic mice. Our data support the hypothesis that RAP-011 has unique biologic effects which prevent or circumvent depletion of mouse splenic iron stores. RAP-011 may, therefore, be an appropriate therapeutic for trials in human anemias characterized by increased expression of hepcidin antimicrobial peptide and iron-restricted erythropoiesis.
抗菌肽铁调素的过度表达是人类缺铁性贫血的一个常见特征。我们研究了C57BL/6小鼠以及抗菌肽铁调素1过表达小鼠对促红细胞生成素或RAP - 011(一种sotatercept的“鼠源化”直系同源物)的红细胞生成反应。Sotatercept是一种可溶性的IIA型激活素受体配体陷阱,目前正在评估其用于治疗与慢性肾病、骨髓增生异常综合征、β地中海贫血和先天性纯红细胞再生障碍性贫血相关的贫血,其作用机制是抑制激活素及其他转化生长因子 - β超家族成员的下游信号传导。我们发现促红细胞生成素和RAP - 011可提高C57BL/6小鼠以及抗菌肽铁调素1过表达小鼠的血红蛋白浓度。虽然促红细胞生成素治疗使C57BL/6小鼠的脾脏铁储备减少,但RAP - 011治疗并未使两种基因型小鼠的脾脏铁储备减少。流式细胞术检测显示,促红细胞生成素治疗的小鼠骨髓红细胞祖细胞表现出缺铁性红细胞生成,表现为转铁蛋白受体免疫染色的中位荧光强度增加。相比之下,RAP - 011治疗的小鼠未表现出相同程度的缺铁性红细胞生成。总之,我们证明了RAP - 011可提高抗菌肽铁调素1转基因小鼠的血红蛋白浓度。我们的数据支持这样的假设,即RAP - 011具有独特的生物学效应,可预防或避免小鼠脾脏铁储备的消耗。因此,RAP - 011可能是针对以抗菌肽铁调素表达增加和缺铁性红细胞生成为特征的人类贫血进行试验的合适治疗药物。