Humphrey Ryan S, Nam Seohee, Wylie Dennis C, Ehrlich Lauren I R
Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX.
Center for Biomedical Research Support, The University of Texas at Austin, Austin, TX.
Blood Neoplasia. 2025 Mar 21;2(3):100095. doi: 10.1016/j.bneo.2025.100095. eCollection 2025 Aug.
T-cell acute lymphoblastic leukemia (T-ALL) is a common pediatric malignancy, and central nervous system (CNS) involvement is associated with inferior prognoses. Here, we show that in the LIM-domain-only-2 transgenic and LN3 mouse models of T-ALL, leukemia blasts infiltrate the CNS, where they colocalize with an altered myeloid compartment. Notably, myeloid cells from the leukemic, but not healthy, CNS were sufficient to support T-ALL survival in vitro, and depletion of myeloid cells in vivo significantly reduced CNS leukemia burden. Among myeloid subsets, macrophages and monocytes from the leukemic CNS most robustly supported T-ALL in vitro. Both T-ALL blasts and leukemia-associated myeloid cells in the CNS expressed elevated levels of adhesion molecules, and inhibition of integrin-mediated adhesion or downstream signaling prevented myeloid cells from supporting survival of T-ALL cells in vitro. Single-cell transcriptomic analyses revealed that leukemia-associated myeloid cells in the CNS undergo transcriptional changes, increasing the expression of genes associated with oxidative phosphorylation while reducing inflammatory signatures. Given the clinical importance of T-ALL relapse in the CNS, we tested whether myeloid cells provide a supportive niche for chemotherapy resistance. T-ALL cells in the CNS that rebounded after chemotherapy retained myeloid dependence in vitro, and myeloid depletion improved responsiveness to chemotherapy, prolonging mouse survival. Altogether, these findings demonstrate that myeloid cells support T-ALL in the CNS and suggest that targeting myeloid cells or mechanisms by which they support T-ALL, in conjunction with conventional chemotherapeutic approaches, could improve current treatment outcomes.
T细胞急性淋巴细胞白血病(T-ALL)是一种常见的儿科恶性肿瘤,中枢神经系统(CNS)受累与预后较差相关。在此,我们表明,在T-ALL的仅含LIM结构域2转基因和LN3小鼠模型中,白血病母细胞浸润CNS,在那里它们与改变的髓系区室共定位。值得注意的是,来自白血病而非健康CNS的髓系细胞足以在体外支持T-ALL存活,体内髓系细胞的清除显著降低了CNS白血病负担。在髓系亚群中,来自白血病CNS的巨噬细胞和单核细胞在体外最有力地支持T-ALL。CNS中的T-ALL母细胞和白血病相关髓系细胞均表达升高水平的黏附分子,整合素介导的黏附或下游信号传导的抑制可阻止髓系细胞在体外支持T-ALL细胞存活。单细胞转录组分析显示,CNS中白血病相关髓系细胞发生转录变化,增加与氧化磷酸化相关基因的表达,同时减少炎症特征。鉴于T-ALL在CNS中复发的临床重要性,我们测试了髓系细胞是否为化疗耐药提供支持性微环境。化疗后反弹的CNS中的T-ALL细胞在体外仍保留对髓系细胞的依赖性,髓系细胞清除改善了对化疗的反应性,延长了小鼠存活时间。总之,这些发现表明髓系细胞在CNS中支持T-ALL,并表明与传统化疗方法联合靶向髓系细胞或其支持T-ALL的机制可改善当前的治疗结果。