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

被引:16
作者
Polikarpov, Dmitry M. [1 ,4 ,5 ]
Campbell, Douglas H. [2 ]
McRobb, Lucinda S. [1 ]
Wu, Jiehua [2 ]
Lund, Maria E. [2 ]
Lu, Yanling [2 ]
Deyev, Sergey M. [3 ]
Davidson, Andrew S. [1 ]
Walsh, Bradley J. [2 ]
Zvyagin, Andrei V. [3 ]
Gillatt, David A. [1 ]
机构
[1] Macquarie Univ, Dept Clin Med, Fac Med Hlth & Human Sci, Sydney, NSW 2109, Australia
[2] Glytherix Ltd, Sydney, NSW 2113, Australia
[3] RAS, Shemyakin Ovchinnikov Inst Bioorgan Chem, Moscow 117997, Russia
[4] Macquarie Univ, ARC Ctr Excellence Nanoscale BioPhoton, Sydney, NSW 2109, Australia
[5] Sechenov Univ, Inst Mol Med, Moscow 119991, Russia
关键词
brain neoplasm; fluorescence-guided surgery; glypican-1; IRDye800CW; Miltuximab; monoclonal antibodies; molecular imaging; CENTRAL-NERVOUS-SYSTEM; MALIGNANT GLIOMA; POOR-PROGNOSIS; CANCER; GLYPICAN-1; RESECTION; SAFETY; CETUXIMAB-IRDYE800; MULTIFORME; NAVIGATION;
D O I
10.3390/cancers12040984
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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((R)), 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((R)) 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((R))-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((R))-IR800 versus 2.4 +/- 0.1 for the control group injected with IgG-IR800 (p = 0.001). Ex vivo assessment of Miltuximab((R))-IR800 biodistribution confirmed its highly specific accumulation in the tumor. The results of this study confirm that Miltuximab((R))-IR800 holds promise for intraoperative fluorescence molecular imaging of GBM and warrants further studies.
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页数:14
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