Basser Russell L, O'Flaherty Elizabeth, Green Michael, Edmonds Maria, Nichol Janet, Menchaca Dora M, Cohen Brian, Begley C Glenn
Centre for Developmental Cancer Therapeutics, Department of Haematology and Medical Oncology, Ludwig Institute for Cancer Research, Royal Melbourne Hospital, 45 Poplar Road, Parkville, Victoria 3052, Australia.
Blood. 2002 Apr 1;99(7):2599-602. doi: 10.1182/blood.v99.7.2599.
Clinical trials of thrombopoietin (TPO), the central regulator of megakaryocytopoiesis, have revealed few side effects associated with its use. We here report a case of pancytopenia associated with the development of neutralizing antibodies to TPO that occurred in a patient who had undergone multicycle chemotherapy with multiple cycles of subcutaneous administration of pegylated recombinant human megakaryocyte growth and development factor. Samples of the patient's bone marrow showed trilineage hypoplasia with absence of myeloid, erythroid, and megakaryocyte progenitor cells but with elevated endogenous levels of erythropoietin, granulocyte colony-stimulating factor, and stem-cell factor. To our knowledge, this is the first report of an aplastic anemia-like syndrome associated with neutralizing antibodies to TPO.
血小板生成素(TPO)是巨核细胞生成的核心调节因子,其临床试验显示使用该药物的副作用很少。我们在此报告一例全血细胞减少症,该病症与针对TPO的中和抗体的产生有关,此情况发生在一名接受多周期化疗并多次皮下注射聚乙二醇化重组人巨核细胞生长和发育因子的患者身上。该患者的骨髓样本显示三系造血细胞发育不全,缺乏髓系、红系和巨核细胞祖细胞,但内源性促红细胞生成素、粒细胞集落刺激因子和干细胞因子水平升高。据我们所知,这是首例与针对TPO的中和抗体相关的再生障碍性贫血样综合征的报告。