Boosting CAR T cell functionality with oncolytic viruses for the treatment of pediatric diffuse midline gliomas. [PDF]
Vazaios K +13 more
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Direct Comparison of MRM-MS and PRM-MS Methods for Quantitative Ganglioside Analysis. [PDF]
Sanni A +4 more
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The Architecture of Immune Escape in Neuroblastoma: Plasticity, Silence and Escape Engineer Immune Blindness. [PDF]
Subramanian P +4 more
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GD2-Targeted Minibody-Drug Conjugates Match the Potency of IgG-Based ADCs in a Mouse Cancer Model. [PDF]
Kalinovsky DV +6 more
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Integrative precision oncology in neuroblastoma: multi-omics biomarkers, molecular targets, and immunotherapeutic strategies. [PDF]
Singh A +8 more
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Pressure-Induced Structural Phase Transition in Gd<sub>2</sub>Ce<sub>2</sub>O<sub>7</sub> Oxide. [PDF]
Lv T +6 more
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Neuroblastoma, a malignant neoplasm of the sympathetic nervous system, is one of the most aggressive pediatric cancers. Patients with stage IV high-risk neuroblastoma receive an intensive multimodal therapy ending with an immunotherapy based on a chimeric monoclonal antibody ch14.18.
Tatjana, Terzic +8 more
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Mimotopes of the disialoganglioside GD2 elicit anti-GD2 antibodies recognising GD2 on melanoma cells
Journal of Clinical Oncology, 200612505 Background: The disialoganglioside GD2, a carbohydrate antigen, is expressed on all tumors of neuroectodermal origin, including melanoma, sarcoma, neuroblastoma and small cell lung cancer. Due to its specific expression on tumor surfaces, GD2 is an attractive target for immunotherapy.
K. H. Brämswig +8 more
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Abstract Background: Breast cancer stem-like cells (BCSCs) are reported to be a major contributing factor for tumor growth and chemotherapy resistance in triple-negative breast cancer (TNBC). We reported that the disialoganglioside GD2 is highly expressed on BCSCs and that targeting GD2 with dinutuximab (chimeric anti-GD2 antibody) in ...
Vivek Anand +7 more
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