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抗 GD2-IRDye800CW 作为神经母细胞瘤荧光引导手术的靶向探针。

Anti-GD2-IRDye800CW as a targeted probe for fluorescence-guided surgery in neuroblastoma.

机构信息

Princess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584 CS, Utrecht, The Netherlands.

Oncode Institute, Hubrecht Institute - KNAW, Utrecht, The Netherlands.

出版信息

Sci Rep. 2020 Oct 19;10(1):17667. doi: 10.1038/s41598-020-74464-4.

Abstract

Neuroblastoma resection represents a major challenge in pediatric surgery, because of the high risk of complications. Fluorescence-guided surgery (FGS) could lower this risk by facilitating discrimination of tumor from normal tissue and is gaining momentum in adult oncology. Here, we provide the first molecular-targeted fluorescent agent for FGS in pediatric oncology, by developing and preclinically evaluating a GD2-specific tracer consisting of the immunotherapeutic antibody dinutuximab-beta, recently approved for neuroblastoma treatment, conjugated to near-infrared (NIR) fluorescent dye IRDye800CW. We demonstrated specific binding of anti-GD2-IRDye800CW to human neuroblastoma cells in vitro and in vivo using xenograft mouse models. Furthermore, we defined an optimal dose of 1 nmol, an imaging time window of 4 days after administration and show that neoadjuvant treatment with anti-GD2 immunotherapy does not interfere with fluorescence imaging. Importantly, as we observed universal, yet heterogeneous expression of GD2 on neuroblastoma tissue of a wide range of patients, we implemented a xenograft model of patient-derived neuroblastoma organoids with differential GD2 expression and show that even low GD2 expressing tumors still provide an adequate real-time fluorescence signal. Hence, the imaging advancement presented in this study offers an opportunity for improving surgery and potentially survival of a broad group of children with neuroblastoma.

摘要

神经母细胞瘤切除术是小儿外科的一大挑战,因为存在很高的并发症风险。荧光引导手术(FGS)可以通过帮助区分肿瘤和正常组织来降低这种风险,并且在成人肿瘤学中正在得到越来越多的应用。在这里,我们通过开发和临床前评估一种由免疫治疗抗体度伐鲁单抗-β组成的 GD2 特异性示踪剂,为儿科肿瘤学中的 FGS 提供了第一个分子靶向荧光剂,该抗体最近被批准用于神经母细胞瘤治疗,并与近红外(NIR)荧光染料 IRDye800CW 结合。我们使用异种移植小鼠模型在体外和体内证明了抗-GD2-IRDye800CW 与人神经母细胞瘤细胞的特异性结合。此外,我们确定了 1 nmol 的最佳剂量,给药后 4 天的成像时间窗口,并表明抗-GD2 免疫治疗的新辅助治疗不会干扰荧光成像。重要的是,由于我们观察到广泛的神经母细胞瘤组织上存在普遍但异质性的 GD2 表达,因此我们实施了具有不同 GD2 表达的患者来源神经母细胞瘤类器官的异种移植模型,并表明即使是低表达 GD2 的肿瘤仍然提供了足够的实时荧光信号。因此,本研究中提出的成像进展为提高广泛的神经母细胞瘤患儿的手术和潜在生存率提供了机会。

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