Hosoi Yoshio
Section of Radiation Biology, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Japan.
Yakugaku Zasshi. 2006 Oct;126(10):841-8. doi: 10.1248/yakushi.126.841.
Total-body irradiation (TBI) with 0.02-0.25 Gy has been reported to have antitumor effects. In mice, low-dose TBI induces tumor growth delay, antimetastatic effects, suppressive effects on the incidence of spontaneous thymiclymphoma, sensitization of tumor to ionizing radiation, and decrease in TD50 value. In artificial metastasis, 0.20 Gy TBI suppressed lung metastasis when it was conducted between 3 h before and 3 h after tumor cell injection into a tail vein. In spontaneous metastasis, 0.15-0.20 Gy TBI suppressed lung metastasis. Irradiation with 0.15 Gy twice a week from 11 weeks of age for 40 weeks significantly suppressed the incidence of spontaneous thymic lymphoma in AKR/J mice, which caused prolonged life span. Low-dose TBI has been used in the clinical treatment of lymphomatous malignancies including chronic lymphocytic leukaemia (CLL) and non-Hodgkin's lymphoma (NHL). The usual practice was to give 0.1 Gy TBI three times a week or 0.15 Gy TBI two times a week to a total dose of 1.5 Gy. Despite this low total dose, low-dose fractionated TBI could induce long-term remissions and was as effective as the chemotherapy to which it was compared. Experimental data suggest that the antitumor effects of low-dose TBI could be explained by immune enhancement, induction of apoptosis, and intrinsic hypersensitivity to low-dose irradiation. Possible mechanisms of immune enhancement are elimination of the T-suppressor subset of lymphocytes and augmentation of the immune response including alteration of cytokine release and enhanced proliferative activity of lymphocytes to mitogenic stimuli.
据报道,全身照射(TBI)剂量为0.02 - 0.25 Gy时具有抗肿瘤作用。在小鼠中,低剂量TBI可诱导肿瘤生长延迟、产生抗转移作用、抑制自发性胸腺淋巴瘤的发生率、使肿瘤对电离辐射敏感,并降低TD50值。在人工转移实验中,当在肿瘤细胞注入尾静脉前3小时至注入后3小时之间进行0.20 Gy的TBI时,可抑制肺转移。在自发性转移实验中,0.15 - 0.20 Gy的TBI可抑制肺转移。从11周龄开始,每周两次给予0.15 Gy照射,持续40周,可显著抑制AKR/J小鼠自发性胸腺淋巴瘤的发生率,从而延长其寿命。低剂量TBI已用于包括慢性淋巴细胞白血病(CLL)和非霍奇金淋巴瘤(NHL)在内的淋巴瘤恶性肿瘤的临床治疗。通常的做法是每周三次给予0.1 Gy的TBI或每周两次给予0.15 Gy的TBI,总剂量为1.5 Gy。尽管总剂量较低,但低剂量分次TBI可诱导长期缓解,且与所比较的化疗效果相当。实验数据表明,低剂量TBI的抗肿瘤作用可通过免疫增强、诱导凋亡以及对低剂量辐射的内在超敏反应来解释。免疫增强的可能机制包括消除淋巴细胞的T抑制亚群以及增强免疫反应,包括细胞因子释放的改变和淋巴细胞对有丝分裂原刺激的增殖活性增强。