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首页> 外文期刊>The Journal of Nuclear Medicine >Intraoperative Near-Infrared Fluorescence Tumor Imaging with Vascular Endothelial Growth Factor and Human Epidermal Growth Factor Receptor 2 Targeting Antibodies
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Intraoperative Near-Infrared Fluorescence Tumor Imaging with Vascular Endothelial Growth Factor and Human Epidermal Growth Factor Receptor 2 Targeting Antibodies

机译:术中血管内皮生长因子和人类表皮生长因子受体2靶向抗体的近红外荧光肿瘤成像。

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id="p-2">Fluorescence imaging is currently attracting much interest as a method for intraoperative tumor detection, but most current tracers lack tumor specificity. Therefore, this technique can be further improved by tumor-specific detection. With tumor-targeted antibodies bound to a radioactive label, tumor-specific SPECT or PET is feasible in the clinical setting. The aim of the present study was to apply antibody-based tumor detection to intraoperative optical imaging, using preclinical in vivo mouse models. >Methods: Anti-vascular endothelial growth factor (VEGF) antibody bevacizumab and anti-human epidermal growth factor receptor (HER) 2 antibody trastuzumab were labeled with the near-infrared (NIR) fluorescence dye IRDye 800CW. Tumor uptake of the fluorescent tracers and their 89Zr-labeled radioactive counterparts for PET was determined in human xenograft-bearing athymic mice during 1 wk after tracer injection, followed by ex vivo biodistribution and pathologic examination. Intraoperative imaging of fluorescent VEGF- or HER2-positive tumor lesions was performed in subcutaneous tumors and in intraperitoneal dissemination tumor models. >Results: Tumor-to-background ratios, with fluorescent imaging, were 1.93 ?± 0.40 for bevacizumab and 2.92 ?± 0.29 for trastuzumab on day 6 after tracer injection. Real-time intraoperative imaging detected tumor lesions at even the submillimeter level in intraperitoneal dissemination tumor models. These results were supported by standard histology, immunohistochemistry, and fluorescence microscopy analyses. >Conclusion: NIR fluorescence-labeled antibodies targeting VEGF or HER2 can be used for highly specific and sensitive detection of tumor lesions in vivo. These preclinical findings encourage future clinical studies with NIR fluorescence-labeled tumor-specific antibodies for intraoperative-guided surgery in cancer patients.
机译:id =“ p-2”>荧光成像作为一种术中肿瘤检测方法目前引起了广泛的兴趣,但是目前大多数示踪剂缺乏肿瘤特异性。因此,可以通过肿瘤特异性检测来进一步改善该技术。通过将靶向肿瘤的抗体与放射性标记物结合,在临床环境中可行肿瘤特异性SPECT或PET。本研究的目的是使用临床前体内小鼠模型将基于抗体的肿瘤检测应用于术中光学成像。 >方法:用近红外(IR)荧光染料IRDye 800CW标记抗血管内皮生长因子(VEGF)抗体贝伐单抗和抗人表皮生长因子受体(HER)2抗体曲妥珠单抗。在示踪剂注射后1周内,在携带人异种移植的无胸腺小鼠中测定荧光示踪剂及其 89 Zr标记的PET的肿瘤吸收,然后进行离体生物分布和病理学检查。在皮下肿瘤和腹膜内播散性肿瘤模型中进行了荧光VEGF-或HER2阳性肿瘤病变的术中成像。 >结果:荧光示踪显示,在注射示踪剂后第6天,贝伐单抗的肿瘤与背景之比为1.93±0.40,曲妥珠单抗为2.92±0.29。实时术中成像甚至在腹膜内播散性肿瘤模型中甚至在亚毫米水平也检测到了肿瘤病变。这些结果得到标准组织学,免疫组织化学和荧光显微镜分析的支持。 >结论:靶向VEGF或HER2的NIR荧光标记抗体可用于体内特异性高灵敏度检测肿瘤病变。这些临床前发现鼓励用NIR荧光标记的肿瘤特异性抗体进行进一步的临床研究,以用于癌症患者的术中指导手术。

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