Oriuchi N, Watanabe N, Sugiyama S, Higuchi T, Imai K, Yamanaka H, Hashimoto M, Kanda H, Endo K
Department of Nuclear Medicine, Gunma University School of Medicine, Maebashi, Japan.
Br J Cancer. 1996 Jun;73(12):1466-72. doi: 10.1038/bjc.1996.278.
Biodistribution of chimeric mouse/human monoclonal antibody against non-specific cross-reacting antigen (chNCA Ab) was studied in athymic mice and patients with metastatic bone disease. 99mTc-chNCA Ab showed a high labelling efficiency, stability and also a high binding ratio to human granulocytes. Since NCA showed cross-reactivity with carcinoembryonic antigen (CEA), animal experiments showed that 99mTc-chNCA Ab was accumulated in the xenografted tumour which expressed CEA, suggesting the preserved immunoreactivity of labelled materials. In the clinical study, injected 99mTc-chNCA Ab formed a high molecular weight complex immediately after intravenous administration and was trapped mainly in liver. The first-phase plasma half-life was 6.4 +/- 1.1 min. None of the patients showed adverse reaction or human antimurine or anti-chimeric antibody in their serum. 99mTc-chNCA Ab demonstrated remarkably different biodistribution between patients and the animal model and showed different pharmacokinetics from other murine and chimeric Abs reported previously. For safety HPLC analysis should be performed before clinical radioimmunodetection or radioimmunotherapy by incubating radiolabelled MAb with human serum under strict conditions.
在无胸腺小鼠和转移性骨病患者中研究了抗非特异性交叉反应抗原嵌合小鼠/人单克隆抗体(chNCA Ab)的生物分布。99mTc-chNCA Ab显示出高标记效率、稳定性以及与人粒细胞的高结合率。由于NCA与癌胚抗原(CEA)显示交叉反应性,动物实验表明99mTc-chNCA Ab在表达CEA的异种移植肿瘤中蓄积,提示标记物保留了免疫反应性。在临床研究中,静脉注射99mTc-chNCA Ab后立即形成高分子量复合物,主要滞留于肝脏。首过血浆半衰期为6.4±1.1分钟。所有患者血清中均未出现不良反应或人抗鼠或抗嵌合抗体。99mTc-chNCA Ab在患者和动物模型之间显示出明显不同的生物分布,并且与先前报道的其他鼠源和嵌合抗体显示出不同的药代动力学。为确保安全,在临床放射免疫检测或放射免疫治疗前,应在严格条件下将放射性标记的单克隆抗体与人血清孵育后进行高效液相色谱分析。