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Near-Infrared Molecular Imaging of Glioblastoma by Miltuximab®-IRDye800CW as a Potential Tool for Fluorescence-Guided Surgery

机译:Miltuximab®-IRDye800CW作为胶体引导手术的潜在工具对胶质母细胞瘤进行近红外分子成像

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摘要

Glioblastoma (GBM) is one of the most aggressive tumors and its 5-year survival is approximately 5%. Fluorescence-guided surgery (FGS) improves the extent of resection and leads to better prognosis. Molecular near-infrared (NIR) imaging appears to outperform conventional FGS, however, novel molecular targets need to be identified in GBM. Proteoglycan glypican-1 (GPC-1) is believed to be such a target as it is highly expressed in GBM and is associated with poor prognosis. We hypothesize that an anti-GPC-1 antibody, Miltuximab , conjugated with the NIR dye, IRDye800CW (IR800), can specifically accumulate in a GBM xenograft and provide high-contrast in vivo fluorescent imaging in rodents following systemic administration. Miltuximab was conjugated with IR800 and intravenously administered to BALB/c nude mice bearing a subcutaneous U-87 GBM hind leg xenograft. Specific accumulation of Miltuximab -IR800 in subcutaneous xenograft tumor was detected 24 h later using an in vivo fluorescence imager. The conjugate did not cause any adverse events in mice and caused strong fluorescence of the tumor with tumor-to-background ratio (TBR) reaching 10.1 ± 2.8. The average TBR over the 10-day period was 5.8 ± 0.6 in mice injected with Miltuximab -IR800 versus 2.4 ± 0.1 for the control group injected with IgG-IR800 ( = 0.001). Ex vivo assessment of Miltuximab -IR800 biodistribution confirmed its highly specific accumulation in the tumor. The results of this study confirm that Miltuximab -IR800 holds promise for intraoperative fluorescence molecular imaging of GBM and warrants further studies.
机译:胶质母细胞瘤(GBM)是最具侵略性的肿瘤之一,其5年生存率约为5%。荧光引导手术(FGS)改善了切除范围,并带来了更好的预后。分子近红外(NIR)成像似乎胜过常规FGS,但是,GBM中需要确定新的分子靶标。蛋白聚糖glypican-1(GPC-1)被认为是这样的靶标,因为它在GBM中高度表达并且与不良预后相关。我们假设与NIR染料IRDye800CW(IR800)共轭的抗GPC-1抗体Miltuximab可以特异性地积聚在GBM异种移植物中,并在全身给药后在啮齿动物中提供高对比度的体内荧光成像。将Miltuximab与IR800偶联,并向带有皮下U-87 GBM后腿异种移植物的BALB / c裸鼠静脉内给药。使用体内荧光成像仪在24小时后检测到Miltuximab -IR800在皮下异种移植肿瘤中的特异性蓄积。该缀合物没有在小鼠中引起任何不良事件,并且引起了肿瘤的强荧光,肿瘤与背景的比率(TBR)达到了10.1±2.8。注射Miltuximab -IR800的小鼠在10天期间的平均TBR为5.8±0.6,而注射IgG-IR800的对照组的平均TBR为2.4±0.1(= 0.001)。 Miltuximab -IR800生物分布的离体评估证实了其在肿瘤中的高度特异性积累。这项研究的结果证实,Miltuximab -IR800对于GBM的术中荧光分子成像具有广阔的前景,值得进一步研究。

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