Beyer G-J, Miederer M, Vranjes-Durić S, Comor J J, Künzi G, Hartley O, Senekowitsch-Schmidtke R, Soloviev D, Buchegger F
Division of Nuclear Medicine, University Hospital of Geneva, 24 Rue Micheli du Crest, 1211 Geneva 14, Switzerland.
Eur J Nucl Med Mol Imaging. 2004 Apr;31(4):547-54. doi: 10.1007/s00259-003-1413-9. Epub 2004 Jan 14.
This study demonstrates high-efficiency sterilisation of single cancer cells in a SCID mouse model of leukaemia using rituximab, a monoclonal antibody that targets CD20, labelled with terbium-149, an alpha-emitting radionuclide. Radio-immunotherapy with 5.5 MBq labelled antibody conjugate (1.11 GBq/mg) 2 days after an intravenous graft of 5.10(6) Daudi cells resulted in tumour-free survival for >120 days in 89% of treated animals. In contrast, all control mice (no treatment or treated with 5 or 300 micro g unlabelled rituximab) developed lymphoma disease. At the end of the study period, 28.4%+/-4% of the long-lived daughter activity remained in the body, of which 91.1% was located in bone tissue and 6.3% in the liver. A relatively high daughter radioactivity concentration was found in the spleen (12%+/-2%/g), suggesting that the killed cancer cells are mainly eliminated through the spleen. This promising preliminary in vivo study suggests that targeted alpha therapy with (149)Tb is worthy of consideration as a new-generation radio-immunotherapeutic approach.
本研究表明,在白血病的SCID小鼠模型中,使用利妥昔单抗(一种靶向CD20的单克隆抗体)标记α发射放射性核素铽 - 149,可实现对单个癌细胞的高效灭菌。在静脉移植5×10⁶个Daudi细胞2天后,用5.5 MBq标记抗体偶联物(1.11 GBq/mg)进行放射免疫治疗,89%的治疗动物实现了>120天的无瘤存活。相比之下,所有对照小鼠(未治疗或用5或300μg未标记利妥昔单抗治疗)均发生淋巴瘤疾病。在研究期结束时,28.4%±4%的长寿命子体活性保留在体内,其中91.1%位于骨组织,6.3%位于肝脏。在脾脏中发现相对较高的子体放射性浓度(12%±2%/g),表明被杀死的癌细胞主要通过脾脏清除。这项有前景的体内初步研究表明,用(149)Tb进行靶向α治疗作为新一代放射免疫治疗方法值得考虑。