Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Pokfulam Road, Hong Kong, Hong Kong, China.
Leuk Res. 2010 Oct;34(10):1390-4. doi: 10.1016/j.leukres.2010.01.028. Epub 2010 Feb 18.
We evaluated the NOD/SCID engraftment of CD34(+) cells from polycythemia vera (PV) and secondary polycythemia patients (SP) and the JAK2V617F clone before and after transplantation. Peripheral blood CD34(+) cells were transplanted intra-femorally. In the injected BM, successful engraftment (>0.1%) occurred in 8/26 mice transplanted with CD34+ cells from 5/13 PV patients (median: 4.26%, range: 0.3-5.56%), in contrast to 0/14 mice from 9 SP patients (P=0.017). The engrafting PV cells were of multi-lineage. JAK2V617F/total JAK2 ratios decreased after transplantation (initial: 65.9% versus 6-week: 13.0%, P=0.001). Essential thrombocythemia (ET) BM cells also exhibited a similar decrease in JAK2V617F clone. The results suggested that events in addition to JAK2V617F are involved in the pathogenesis of PV and ET.
我们评估了原发性骨髓纤维化(PV)和继发性骨髓纤维化(SP)患者 CD34(+)细胞的 NOD/SCID 嵌合体,并在移植前后评估了 JAK2V617F 克隆。外周血 CD34(+)细胞通过股骨内注射进行移植。在注射的 BM 中,来自 5/13 名 PV 患者的 CD34+细胞成功植入了 8/26 只小鼠(中位数:4.26%,范围:0.3-5.56%),而来自 9 名 SP 患者的 14 只小鼠无一例成功植入(P=0.017)。植入的 PV 细胞为多系。移植后 JAK2V617F/总 JAK2 比值降低(初始:65.9%,6 周时:13.0%,P=0.001)。特发性血小板增多症(ET)BM 细胞的 JAK2V617F 克隆也出现类似的减少。结果表明,除 JAK2V617F 外,还有其他事件参与了 PV 和 ET 的发病机制。