Program of Immunology and Immunotherapy, Cima Universidad de Navarra, Pamplona, Spain.
Navarra Institute for Health Research (IDISNA), Pamplona, Spain.
Clin Cancer Res. 2024 Sep 13;30(18):4131-4142. doi: 10.1158/1078-0432.CCR-23-3860.
Patients with cancer frequently undergo radiotherapy in their clinical management with unintended irradiation of blood vessels and copiously irrigated organs in which polymorphonuclear leukocytes circulate. Following the observation that such low doses of ionizing radiation are able to induce neutrophils to extrude neutrophil extracellular traps (NET), we have investigated the mechanisms, consequences, and occurrence of such phenomena in patients undergoing radiotherapy.
NETosis was analyzed in cultures of neutrophils isolated from healthy donors, patients with cancer, and cancer-bearing mice under confocal microscopy. Cocultures of radiation-induced NETs, immune effector lymphocytes, and tumor cells were used to study the effects of irradiation-induced NETs on immune cytotoxicity. Radiation-induced NETs were intravenously injected to mice for assessing their effects on metastasis. Circulating NETs in irradiated patients with cancer were measured using ELISA methods for detecting MPO-DNA complexes and citrullinated histone 3.
Irradiation of neutrophils with very low γ-radiation doses (0.5-1 Gy) elicits NET formation in a manner dependent on oxidative stress, NADPH oxidase activity, and autocrine IL8. Radiation-induced NETs interfere with NK cell and T-cell cytotoxicity. As a consequence, preinjection of irradiation-induced NETs increases the number of successful metastases in mouse tumor models. Increases in circulating NETs were readily detected in two prospective series of patients following the first fraction of their radiotherapy courses.
NETosis is induced by low-dose ionizing irradiation in a neutrophil-intrinsic fashion, and radiation-induced NETs are able to interfere with immune-mediated cytotoxicity. Radiation-induced NETs foster metastasis in mouse models and can be detected in the circulation of patients undergoing conventional radiotherapy treatments. See related commentary by Mowery and Luke, p. 3965.
在癌症患者的临床治疗中,经常进行放射治疗,导致血管和大量冲洗的器官受到意外照射,其中循环着多形核白细胞。观察到这种低剂量电离辐射能够诱导中性粒细胞释放中性粒细胞细胞外陷阱(NET)后,我们研究了在接受放射治疗的患者中发生这种现象的机制、后果和发生情况。
通过共聚焦显微镜分析从健康供体、癌症患者和荷瘤小鼠中分离的中性粒细胞培养物中的 NETosis。将辐射诱导的 NET 与免疫效应淋巴细胞和肿瘤细胞共培养,研究辐射诱导的 NET 对免疫细胞毒性的影响。将辐射诱导的 NET 静脉注射到小鼠中,以评估其对转移的影响。使用 ELISA 方法测量接受放射治疗的癌症患者循环中的 NETs,以检测 MPO-DNA 复合物和瓜氨酸化组蛋白 3。
用非常低的γ辐射剂量(0.5-1 Gy)辐照中性粒细胞会诱导 NET 形成,这种形成方式依赖于氧化应激、NADPH 氧化酶活性和自分泌 IL8。辐射诱导的 NET 会干扰 NK 细胞和 T 细胞的细胞毒性。因此,在小鼠肿瘤模型中,预先注射辐射诱导的 NET 会增加成功转移的数量。在两个前瞻性系列的患者中,在接受放射治疗的第一部分后,很容易检测到循环 NETs 的增加。
低剂量电离辐射会以中性粒细胞内在的方式诱导 NETosis,辐射诱导的 NET 能够干扰免疫介导的细胞毒性。辐射诱导的 NET 促进了小鼠模型中的转移,并且可以在接受常规放射治疗的患者的循环中检测到。请参阅 Mowery 和 Luke 的相关评论,第 3965 页。