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慢性粒单核细胞白血病中 I 型干扰素上调和参与单核细胞生成的基因失调。

Type I interferon upregulation and deregulation of genes involved in monopoiesis in chronic myelomonocytic leukemia.

机构信息

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

出版信息

Leuk Res. 2021 Feb;101:106511. doi: 10.1016/j.leukres.2021.106511. Epub 2021 Jan 19.

Abstract

Chronic myelomonocytic leukemia (CMML) is characterized by myelomonocytic bias and monocytic proliferation. Whether cell-intrinsic innate immune or inflammatory upregulation mediate disease pathogenesis and phenotype or whether the degree of aberrant monocytic differentiation influences outcomes remains unclear. We compared the transcriptomic features of bone marrow CD34+ cells from 19 patients with CMML and compared to healthy individuals. A total of 1495 genes had significantly differential expression in CMML (q<0.05, fold change>2), including 1271 genes that were significantly upregulated and 224 that were significantly downregulated in CMML. Top upregulated genes were associated with interferon (IFN) alpha and beta signaling, chemokine receptors, IFN gamma, G protein-coupled receptor ligand signaling, and genes involved in immunomodulatory interactions between lymphoid and non-lymphoid cells. Additionally, 6 gene sets were differentially upregulated and 139 were significantly downregulated in patients with myeloproliferative compared to myelodysplastic CMML. A total of 23 genes involved in regulation of monopoiesis were upregulated in CMML compared to healthy controls. We developed a prediction model using Cox regression including 3 of these genes, which differentiated patients into two prognostic subsets with distinct survival outcomes. This data warrants further evaluation of the roles and therapeutic potential of type I IFN signaling and monopoiesis in CMML.

摘要

慢性粒单核细胞白血病(CMML)的特征为骨髓中粒系和单核系细胞增生,单核细胞增多。细胞内固有免疫或炎症上调是否介导疾病发病机制和表型,或者异常单核细胞分化程度是否影响预后尚不清楚。我们比较了 19 例 CMML 患者和健康个体骨髓 CD34+细胞的转录组特征。CMML 中有 1495 个基因的表达存在显著差异(q<0.05,倍数变化>2),其中 1271 个基因上调,224 个基因下调。上调的基因与干扰素(IFN)α和β信号、趋化因子受体、IFNγ、G 蛋白偶联受体配体信号以及参与淋巴样和非淋巴样细胞之间免疫调节相互作用的基因有关。此外,与骨髓增生性 CMML 相比,骨髓增生异常性 CMML 中有 6 个基因集上调,139 个基因显著下调。与健康对照组相比,CMML 中有 23 个参与单核细胞生成调控的基因上调。我们使用 Cox 回归建立了一个包含 3 个基因的预测模型,该模型将患者分为具有不同生存结果的两个预后亚组。这些数据进一步验证了 I 型 IFN 信号和单核细胞生成在 CMML 中的作用和治疗潜力。

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