血小板生成素
血小板生成素
罗米普洛斯蒂姆
埃尔特罗姆博帕格
医学
血小板生成素受体
药理学
血小板
免疫学
巨核细胞
免疫性血小板减少症
生物
造血
干细胞
细胞生物学
作者
Roberto Stasi,Jenny Bosworth,Elizabeth Rhodes,Michael Shannon,Fenella Willis,E. C. Gordon‐Smith
出处
期刊:Blood Reviews
[Elsevier]
日期:2010-07-01
卷期号:24 (4-5): 179-190
被引量:52
标识
DOI:10.1016/j.blre.2010.04.002
摘要
Thrombopoietin (TPO) is the key cytokine involved in thrombopoiesis, and is the endogenous ligand for the thrombopoietin receptor that is expressed on the surface of platelets, megakaryocytes, and megakaryocytic precursors. First-generation thrombopoietic agents were recombinant forms of human TPO, and their development was discontinued after prolonged thrombocytopenia due to neutralizing auto-antibodies cross-reacting with endogenous TPO was observed. Second-generation thrombopoiesis-stimulating molecules are now available, which have unique pharmacological properties and no sequence homology to endogenous TPO. Two of these new agents, romiplostim and eltrombopag, have already completed phase III trials in primary immune thrombocytopenia and have been granted marketing authorization for use in this disease. Phase II and III trials with these novel drugs are ongoing in other conditions characterized by thrombocytopenia, such as chemotherapy, chronic liver disease, and the myelodysplastic syndromes. Most of the other second-generation thrombopoietic growth factors are in early phase clinical development.
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