Jing Hua, Weidensteiner Claudia, Reichardt Wilfried, Gaedicke Simone, Zhu Xuekai, Grosu Anca-Ligia, Kobayashi Hisataka, Niedermann Gabriele
1. Dept. for Radiation Oncology, University Hospital Freiburg, D-79106 Freiburg, Germany; 3. German Cancer Consortium (DKTK), Freiburg, and German Cancer Research Centre (DKFZ), D-69121 Heidelberg, Germany.
2. Radiology Medical Physics, University Hospital Freiburg, D-79106 Freiburg, Germany.
Theranostics. 2016 Apr 12;6(6):862-74. doi: 10.7150/thno.12890. eCollection 2016.
Near-infrared photoimmunotherapy (NIR-PIT), which employs monoclonal antibody (mAb)-phototoxic phthalocyanine dye IR700 conjugates, permits the specific, image-guided and spatiotemporally controlled elimination of tumor cells. Here, we report the highly efficient NIR-PIT of human tumor xenografts initiated from patient-derived cancer stem cells (CSCs). Using glioblastoma stem cells (GBM-SCs) expressing the prototypic CSC marker AC133/CD133, we also demonstrate here for the first time that NIR-PIT is highly effective against brain tumors. The intravenously injected theranostic AC133 mAb conjugate enabled the non-invasive detection of orthotopic gliomas by NIR fluorescence imaging, and reached AC133+ GBM-SCs at the invasive tumor front. AC133-targeted NIR-PIT induced the rapid cell death of AC133+ GBM-SCs and thereby strong shrinkage of both subcutaneous and invasively growing brain tumors. A single round of NIR-PIT extended the overall survival of mice with established orthotopic gliomas by more than a factor of two, even though the harmless NIR light was applied through the intact skull. Humanised versions of this theranostic agent may facilitate intraoperative imaging and histopathological evaluation of tumor borders and enable the highly specific and efficient eradication of CSCs.
近红外光免疫疗法(NIR-PIT)利用单克隆抗体(mAb)-光毒性酞菁染料IR700偶联物,能够特异性、图像引导且时空可控地消除肿瘤细胞。在此,我们报告了源自患者癌症干细胞(CSC)的人肿瘤异种移植模型的高效NIR-PIT。利用表达典型CSC标志物AC133/CD133的胶质母细胞瘤干细胞(GBM-SCs),我们还首次证明NIR-PIT对脑肿瘤高度有效。静脉注射的治疗诊断性AC133单克隆抗体偶联物可通过近红外荧光成像对原位胶质瘤进行无创检测,并在侵袭性肿瘤前沿到达AC133+ GBM-SCs。以AC133为靶点的NIR-PIT诱导AC133+ GBM-SCs快速细胞死亡,从而使皮下和侵袭性生长的脑肿瘤显著缩小。尽管通过完整颅骨施加无害的近红外光,但一轮NIR-PIT使已建立原位胶质瘤的小鼠总体生存期延长了两倍多。这种治疗诊断剂的人源化版本可能有助于术中对肿瘤边界进行成像和组织病理学评估,并能够高度特异性且高效地根除CSC。
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