Kornberg A, Fibach E, Treves A, Goldfarb A, Rachmilewitz E A
Br J Haematol. 1982 Dec;52(4):573-8. doi: 10.1111/j.1365-2141.1982.tb03933.x.
The ability of circulating progenitor cells from patients with polycythaemia vera (PV) and myelofibrosis with myeloid metaplasia (MMM) to develop erythroid colonies was studied in cultures with and without erythropoietin. In all normal controls, patients with secondary polycythaemia and MMM, erythroid colonies developed only after the addition of erythropoietin. Only in patients with PV, both in the active and spent phases of the disease, erythroid colonies developed in the absence of erythropoietin. The results indicate the perpetuation of erythropoietin-dependent, as well as erythropoietin-independent progenitors in both phases of this disease. Although spent PV often clinically resembles MMM, there is a basic difference in the behaviour of the circulating erythroid progenitors in these diseases which may serve as a useful tool in discriminating MMM from spent PV, when there is no history of active PV.
研究了真性红细胞增多症(PV)和骨髓纤维化伴髓外化生(MMM)患者循环祖细胞在有和没有促红细胞生成素的培养物中形成红系集落的能力。在所有正常对照、继发性红细胞增多症患者和MMM患者中,只有添加促红细胞生成素后才会形成红系集落。只有PV患者,无论在疾病的活动期还是静止期,在没有促红细胞生成素的情况下也会形成红系集落。结果表明,在这种疾病的两个阶段中,促红细胞生成素依赖性和促红细胞生成素非依赖性祖细胞都持续存在。尽管静止期PV在临床上常与MMM相似,但这些疾病中循环红系祖细胞的行为存在根本差异,这在没有活动性PV病史时,可作为区分MMM和静止期PV的有用工具。