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Imaging and Selective Elimination of Glioblastoma Stem Cells with Theranostic Near-Infrared-Labeled CD133-Specific Antibodies.
Jing, Hua; Weidensteiner, Claudia; Reichardt, Wilfried; Gaedicke, Simone; Zhu, Xuekai; Grosu, Anca-Ligia; Kobayashi, Hisataka; Niedermann, Gabriele.
Affiliation
  • Jing H; 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.
  • Weidensteiner C; 2. Radiology Medical Physics, University Hospital Freiburg, D-79106 Freiburg, Germany.
  • Reichardt W; 2. Radiology Medical Physics, University Hospital Freiburg, D-79106 Freiburg, Germany.
  • Gaedicke S; 1. Dept. for Radiation Oncology, University Hospital Freiburg, D-79106 Freiburg, Germany.
  • Zhu X; 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.
  • Grosu AL; 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.
  • Kobayashi H; 4. Molecular Imaging Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Niedermann G; 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.
Theranostics ; 6(6): 862-74, 2016.
Article in En | MEDLINE | ID: mdl-27162556
ABSTRACT
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.
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Full text: 1 Collection: 01-internacional Health context: 6_ODS3_enfermedades_notrasmisibles Database: MEDLINE Main subject: Phototherapy / Glioblastoma / Theranostic Nanomedicine / AC133 Antigen / Immunotherapy Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Theranostics Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 6_ODS3_enfermedades_notrasmisibles Database: MEDLINE Main subject: Phototherapy / Glioblastoma / Theranostic Nanomedicine / AC133 Antigen / Immunotherapy Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Theranostics Year: 2016 Document type: Article