Department of Internal Medicine III with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Salzburg Cancer Research Institute - Laboratory for Immunological and Molecular Cancer Research, Salzburg, Austria; and.
Blood. 2019 Nov 14;134(20):1717-1729. doi: 10.1182/blood.2019000973.
Chronic lymphocytic leukemia (CLL) is a heterogenous disease that is highly dependent on a cross talk of CLL cells with the microenvironment, in particular with T cells. T cells derived from CLL patients or murine CLL models are skewed to an antigen-experienced T-cell subset, indicating a certain degree of antitumor recognition, but they are also exhausted, preventing an effective antitumor immune response. Here we describe a novel mechanism of CLL tumor immune evasion that is independent of T-cell exhaustion, using B-cell-specific deletion of the transcription factor IRF4 (interferon regulatory factor 4) in Tcl-1 transgenic mice developing a murine CLL highly similar to the human disease. We show enhanced CLL disease progression in IRF4-deficient Tcl-1 tg mice, associated with a severe downregulation of genes involved in T-cell activation, including genes involved in antigen processing/presentation and T-cell costimulation, which massively reduced T-cell subset skewing and exhaustion. We found a strong analogy in the human disease, with inferior prognosis of CLL patients with low IRF4 expression in independent CLL patient cohorts, failed T-cell skewing to antigen-experienced subsets, decreased costimulation capacity, and downregulation of genes involved in T-cell activation. These results have therapeutic relevance because our findings on molecular mechanisms of immune privilege may be responsible for the failure of immune-therapeutic strategies in CLL and may lead to improved targeting in the future.
慢性淋巴细胞白血病(CLL)是一种异质性疾病,高度依赖 CLL 细胞与微环境的串扰,特别是与 T 细胞。源自 CLL 患者或鼠 CLL 模型的 T 细胞偏向于抗原经验的 T 细胞亚群,表明具有一定程度的抗肿瘤识别,但它们也已耗尽,从而阻止了有效的抗肿瘤免疫反应。在这里,我们描述了一种 CLL 肿瘤免疫逃避的新机制,该机制不依赖于 T 细胞衰竭,使用 B 细胞特异性缺失 T 细胞转录因子 IRF4(干扰素调节因子 4),在 Tcl-1 转基因小鼠中发展出与人疾病高度相似的鼠 CLL。我们显示,IRF4 缺陷的 Tcl-1 tg 小鼠中的 CLL 疾病进展增强,与涉及 T 细胞激活的基因的严重下调相关,包括涉及抗原加工/呈递和 T 细胞共刺激的基因,这大大减少了 T 细胞亚群的偏向和衰竭。我们在人类疾病中发现了很强的相似性,在独立的 CLL 患者队列中,IRF4 表达水平低的 CLL 患者预后较差,抗原经验性亚群的 T 细胞偏向失败,共刺激能力下降,以及参与 T 细胞激活的基因下调。这些结果具有治疗相关性,因为我们对免疫特权分子机制的研究结果可能是导致 CLL 免疫治疗策略失败的原因,并可能导致未来的靶向治疗得到改善。