Geissler Klaus, Jäger Eva, Barna Agnes, Sliwa Thamer, Knöbl Paul, Schwarzinger Ilse, Gisslinger Heinz, Valent Peter
5th Medical Department with Hematology, Oncology and Palliative Medicine, Hospital Hietzing, Vienna, Austria.
Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Eur J Haematol. 2016 Dec;97(6):562-567. doi: 10.1111/ejh.12773. Epub 2016 Jun 15.
In chronic myelomonocytic leukemia (CMML), colony-forming units granulocyte/macrophage (CFU-GM), which grow in vitro in the absence of exogenous growth factors, arise from the abnormal clone that is responsible for the overproduction of granulomonocytic cells. Previous in vitro findings including ours suggest that divergent molecular aberrations in CMML seem to converge within the GM-CSF signaling pathway. As JAK2 is a sentinel kinase in this pathway, JAK2 inhibition may be an attractive treatment approach in CMML. We investigated the in vitro effects of the specific JAK2 inhibitor TG101209 on the autonomous CFU-GM formation from peripheral blood mononuclear cells of patients with CMML. TG101209 was found to either block or strongly inhibit spontaneous CFU-GM growth in all 10 patients tested. This inhibitory effect was dose dependent and significantly more pronounced as compared to the inhibitory effect on stimulated CFU-GM growth from normal individuals. In a CMML patient with splenomegaly, who was treated with the JAK1/2 inhibitor ruxolitinib off label, we can demonstrate a spleen response and the disappearance of constitutional symptoms which was associated with a decrease in autonomous CFU-GM formation ex vivo. Pharmacological JAK2 inhibition may be an interesting approach to be systematically studied in patients with CMML.
在慢性粒单核细胞白血病(CMML)中,粒细胞/巨噬细胞集落形成单位(CFU-GM)在无外源性生长因子的情况下于体外生长,源自导致粒单核细胞过度产生的异常克隆。包括我们的研究在内,先前的体外研究结果表明,CMML中不同的分子异常似乎在GM-CSF信号通路中汇聚。由于JAK2是该通路中的一个关键激酶,抑制JAK2可能是CMML中一种有吸引力的治疗方法。我们研究了特异性JAK2抑制剂TG101209对CMML患者外周血单个核细胞自主形成CFU-GM的体外作用。发现TG101209在所有10例受试患者中均能阻断或强烈抑制自发的CFU-GM生长。这种抑制作用呈剂量依赖性,与对正常个体刺激的CFU-GM生长的抑制作用相比明显更显著。在一名接受JAK1/2抑制剂芦可替尼非标签治疗的脾肿大CMML患者中,我们证实了脾脏反应以及全身症状的消失,这与体外自主CFU-GM形成的减少有关。药理学上抑制JAK2可能是一种值得在CMML患者中进行系统研究的有趣方法。