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Monocytic myeloid‐derived suppressor cells as prognostic factor in chronic myeloid leukaemia patients treated with dasatinib

机译:单核细胞霉菌衍生的抑制细胞作为慢性髓性白血病患者的预后因子,达斯替尼治疗

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Abstract Myeloid suppressor cells are a heterogeneous group of myeloid cells that are increased in patients with chronic myeloid leukaemia (CML) inducing T cell tolerance. In this study, we found that therapy with tyrosine kinase inhibitors (TKI) decreased the percentage of granulocytic MDSC, but only patients treated with dasatinib showed a significant reduction in the monocytic subset (M-MDSC). Moreover, a positive correlation was observed between number of persistent M-MDSC and the value of major molecular response in dasatinib-treated patients. Serum and exosomes from patients with CML induced conversion of monocytes from healthy volunteers into immunosuppressive M-MDSC, suggesting a bidirectional crosstalk between CML cells and MDSC. Overall, we identified M-MDSC as prognostic factors in patients treated with dasatinib. It might be of interest to understand whether MDSC may be a candidate predictive markers of relapse risk following TKI discontinuation, suggesting their potential significance as practice of precision medicine.
机译:摘要骨髓抑制细胞是慢性骨髓性白血病(CML)诱导T细胞耐受性的患者中增加的骨髓细胞的异质组。在这项研究中,我们发现用酪氨酸激酶抑制剂(TKI)的治疗降低了粒细胞MDSC的百分比,但只有用达斯替尼处理的患者才表现出单核细胞子集(MSC)的显着降低。此外,在持久性M-MDSC的数量与达斯替尼治疗的患者的主要分子反应的数量之间观察到阳性相关性。来自CML患者的血清和外来诱导从健康志愿者转化为免疫抑制MSC的单核细胞转化,表明CML细胞和MDSC之间的双向串扰。总体而言,我们将MSC鉴定为用达斯替尼治疗的患者的预后因素。它可能有兴趣了解MDSC是否可能是TKI停止后的复发风险的候选预测标志,表明其作为精密药物实践的潜在意义。

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