Metjian Ara, Abrams Charles S
Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Biologics. 2009;3:499-513. Epub 2009 Dec 29.
Decades of basic science and clinical research have led to an increased understanding of the pathophysiology of immune thrombocytopenic purpura (ITP), the processes underlying thrombopoiesis, and the treatment of chronic ITP. Now, new agents are available to treat ITP in a nonimmunosuppressive fashion. Lessons learned from the clinical trials of recombinant human thrombopoietin (TPO) have led to the development of a novel class of compounds: nonimmunogenic agonists of the thrombopoietin receptor. Representing the first nonimmunosuppressive agents to treat chronic refractory ITP in decades, medications such as romiplostim and eltrombopag were recently approved by the US Food and Drug Administration. These new agents offer physicians a new tool for treating difficult cases of ITP in their medical armamentarium. Additional TPO mimetics are also being developed that show promise in vitro, and await future development.
数十年来的基础科学和临床研究增进了人们对免疫性血小板减少性紫癜(ITP)的病理生理学、血小板生成过程以及慢性ITP治疗的理解。如今,有了以非免疫抑制方式治疗ITP的新型药物。从重组人血小板生成素(TPO)的临床试验中吸取的经验教训促使了一类新型化合物的研发:血小板生成素受体的非免疫原性激动剂。罗米司亭和艾曲泊帕等药物作为数十年来首批用于治疗慢性难治性ITP的非免疫抑制药物,最近已获美国食品药品监督管理局批准。这些新型药物为医生治疗ITP疑难病例提供了一种新的医疗手段。其他血小板生成素模拟物也正在研发中,它们在体外显示出了前景,有待进一步开发。