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用于放射免疫治疗的铼-186-巯基乙酰三甘氨酸标记单克隆抗体:荷瘤裸鼠的体外评估、体内动力学及剂量测定

Rhenium-186-mercaptoacetyltriglycine-labeled monoclonal antibody for radioimmunotherapy: in vitro assessment, in vivo kinetics and dosimetry in tumor-bearing nude mice.

作者信息

Kinuya S, Yokoyama K, Tega H, Hiramatsu T, Konishi S, Yamamoto W, Shuke N, Aburano T, Watanabe N, Takayama T, Michigishi T, Tonami N

机构信息

Department of Nuclear Medicine, Kanazawa University School of Medicine.

出版信息

Jpn J Cancer Res. 1998 Aug;89(8):870-8. doi: 10.1111/j.1349-7006.1998.tb00642.x.

Abstract

Stability and immunoreactivity of 186Re-labeled monoclonal antibody were examined, and its in vivo kinetics was investigated in tumor-bearing Balb/c nu/nu female mice to assess the feasibility of using it in radioimmunotherapy (RIT). A murine IgG1, A7, against a 45 kD glycoprotein in human colon cancer was radiolabeled with 186Re by using a chelating method with a mercaptoacetyltriglycine (MAG3). 186Re-MAG3 complex was conjugated to A7 after esterification of 186Re-MAG3 with tetrafluorophenol (TFP). The efficiency of 186Re-MAG3-TFP production and the labeling efficiency of A7 were 51-59% and 57-60%, respectively. Immunoreactivity of purified 186Re-MAG3-A7 was 68.2% at infinite antigen excess. In 0.9% NaCl at 4 degrees C, the radioactivity (12.7 MBq/mg, 3.55 MBq/ml) dissociated with time from 186Re-MAG3-A7 as a small molecular weight moiety because of autoradiolysis. The addition of ascorbic acid, 5 mg/ml, as a radioprotectant or storage at -80 degrees C could effectively prevent the radiolysis of 186Re-MAG3-A7 for 7 days. Immunoreactivity of 186Re-MAG3-A7, 6.70 MBq/mg (6.66 MBq/ml), stored in the presence of ascorbic acid was well retained up to 8 days after the preparation. In colon cancer xenografted mice, 31.0% of the injected dose/g of 186Re-MAG3-A7 had accumulated in the tumors at 24 h postinjection. Estimated radiation dose to tumors was 14.9 cGy/37 kBq up to 8 days postinjection which was 12-fold greater than the whole-body radiation dose. These in vivo characteristics were superior to those of A7 labeled with radioiodine, affording greater therapeutic ratios than 131I-A7. Because of the better image quality of 186Re-MAG3-A7 as well as more favorable dosimetry, 186Re-MAG3-A7 would be a better choice for RIT of colon cancer than 131I-A7. These results indicated the feasibility of RIT with 186Re-MAG3-A7, though the prevention of radiolysis of the labeled antibody should be considered.

摘要

检测了186Re标记的单克隆抗体的稳定性和免疫反应性,并在荷瘤Balb/c nu/nu雌性小鼠中研究了其体内动力学,以评估将其用于放射免疫治疗(RIT)的可行性。通过使用巯基乙酰三甘氨酸(MAG3)的螯合方法,用186Re对一种针对人结肠癌中45 kD糖蛋白的鼠IgG1(A7)进行放射性标记。186Re-MAG3与四氟苯酚(TFP)酯化后与A7偶联。186Re-MAG3-TFP的制备效率和A7的标记效率分别为51-59%和57-60%。纯化的186Re-MAG3-A7在无限抗原过量时的免疫反应性为68.2%。在4℃的0.9%氯化钠中,由于自身辐射分解,放射性(12.7 MBq/mg,3.55 MBq/ml)以小分子部分的形式随时间从186Re-MAG3-A7解离。添加5 mg/ml的抗坏血酸作为辐射防护剂或在-80℃储存可有效防止186Re-MAG3-A7的辐射分解7天。在抗坏血酸存在下储存的186Re-MAG3-A7(6.70 MBq/mg,6.66 MBq/ml)的免疫反应性在制备后长达8天仍能很好地保留。在结肠癌异种移植小鼠中,注射后24小时,每克注射剂量的186Re-MAG3-A7中有31.0%积聚在肿瘤中。注射后长达8天,估计肿瘤的辐射剂量为14.9 cGy/37 kBq,比全身辐射剂量高12倍。这些体内特性优于用放射性碘标记的A7,治疗比高于131I-A7。由于186Re-MAG3-A7具有更好的图像质量以及更有利的剂量学,对于结肠癌的RIT,186Re-MAG3-A7将是比131I-A7更好的选择。这些结果表明了用186Re-MAG3-A7进行RIT的可行性,不过应考虑防止标记抗体的辐射分解。

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