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首页> 外文期刊>The Journal of Nuclear Medicine >Development of 124I Immuno-PET Targeting Tumor Vascular TEM1/Endosialin
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Development of 124I Immuno-PET Targeting Tumor Vascular TEM1/Endosialin

机译:靶向肿瘤血管TEM1 / Endosialin的124I免疫PET的开发

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id="p-3">Tumor endothelial marker 1 (TEM1/endosialin) is a tumor vascular marker highly overexpressed in multiple human cancers with minimal expression in normal adult tissue. In this study, we report the preparation and evaluation of 124I-MORAb-004, a humanized monoclonal antibody targeting an extracellular epitope of human TEM1 (hTEM1), for its ability to specifically and sensitively detect vascular cells expressing hTEM1 in vivo. >Methods: MORAb-004 was directly iodinated with 125I and 124I, and in vitro binding and internalization parameters were characterized. The in vivo behavior of radioiodinated MORAb-004 was characterized in mice bearing subcutaneous ID8 tumors enriched with mouse endothelial cells expressing hTEM1 and by biodistribution and small-animal immuno-PET studies. >Results: MORAb-004 was radiolabeled with high efficiency and isolated in high purity. In vitro studies demonstrated specific and sensitive binding of MORAb-004 to MS1 mouse endothelial cells expressing hTEM1, with no binding to control MS1 cells. 125I-MORAb-004 and 124I-MORAb-004 both had an immunoreactivity of approximately 90%. In vivo biodistribution experiments revealed rapid, highly specific and sensitive uptake of MORAb-004 in MS1-TEM1 tumors at 4 h (153.2 ?± 22.2 percentage injected dose per gram [%ID/g]), 24 h (127.1 ?± 42.9 %ID/g), 48 h (130.3 ?± 32.4 %ID/g), 72 h (160.9 ?± 32.1 %ID/g), and 6 d (10.7 ?± 1.8 %ID/g). Excellent image contrast was observed with 124I-immuno-PET. MORAb-004 uptake was statistically higher in TEM1-positive tumors than in control tumors. Binding specificity was confirmed by blocking studies using excess nonlabeled MORAb-004. >Conclusion: In our preclinical model, with hTEM1 exclusively expressed on engineered murine endothelial cells that integrate into the tumor vasculature, 124I-MORAb-004 displays high tumor-to-background tissue contrast for detection of hTEM1 in easily accessible tumor vascular compartments. These studies strongly suggest the clinical utility of 124I-MORAb-004 immuno-PET in assessing TEM1 tumor-status.
机译:id =“ p-3”>肿瘤内皮标记物1(TEM1 / endosialin)是在多种人类癌症中高度过表达且在正常成人组织中表达最少的肿瘤血管标记。在这项研究中,我们报告了针对人TEM1(hTEM1)细胞外表位的人源化单克隆抗体 124 I-MORAb-004的制备和评估,该抗体具有特异性和灵敏地检测血管细胞的能力在体内表达hTEM1。 >方法:将MORAb-004直接用 125 I和 124 I碘化,并表征其体外结合和内在化参数。放射性碘化的MORAb-004的体内行为在携带有表达hTEM1的小鼠内皮细胞的皮下ID8肿瘤的小鼠中进行了表征,并通过生物分布和小动物免疫PET研究进行了表征。 >结果:对MORAb-004进行了高效放射性标记,并进行了高纯度分离。体外研究表明,MORAb-004与表达hTEM1的MS1小鼠内皮细胞具有特异性和敏感性结合,而与对照MS1细胞没有结合。 125 I-MORAb-004和 124 I-MORAb-004都具有大约90%的免疫反应性。体内生物分布实验显示,在4小时(每克注射剂量的153.2?±22.2百分比注射剂量[%ID / g]),24小时(127.1?±42.9%)的MS1-TEM1肿瘤中,MORAb-004快速,高度特异性和灵敏地摄取。 ID / g),48小时(130.3±32.4%ID / g),72小时(160.9±32.1%ID / g)和6天(10.7±1.8%ID / g)。用 124 I-immuno-PET观察到极好的图像对比度。 TEM1阳性肿瘤中MORAb-004的摄取在统计学上高于对照肿瘤。通过使用过量的未标记MORAb-004的阻断研究证实了结合特异性。 >结论:在我们的临床前模型中,hTEM1仅在整合到肿瘤脉管系统中的工程鼠内皮细胞上表达, 124 I-MORAb-004显示出很高的肿瘤背景组织对比剂,用于在易于接近的肿瘤血管腔中检测hTEM1。这些研究强烈暗示了 124 I-MORAb-004免疫PET在评估TEM1肿瘤状态方面的临床实用性。

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