| Vol. 21.38 – 2 November, 2020 |
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| Using a self-assembling nanoparticle vaccine that links neoantigen peptides to a Toll-like receptor 7/8 agonist, researchers showed how the route and dose altered the magnitude and quality of neoantigen-specific CD8+ T cells. [Nature Immunology] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| In homeostatic skeletal muscle, scientists identified two quiescent stem-cell states distinguished by relative CD34 expression: CD34High, with stemness properties, and CD34Low, committed to myogenic differentiation. [Nature Cell Biology] |
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| To facilitate pathogenesis studies in vivo, scientists developed an inducible CRISPR interference system that enabled genome-wide fitness testing in one sequencing step [Cell Host & Microbe] |
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| Scientists report a non-conventional, T cell-intrinsic function for Nod2 in suppression of Th17 immunity and experimental uveitis. [Nature Communications] |
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| Investigators constructed minigene circuits based on the CRISPReader, a technology used to control promoter-less gene expression in a robust manner. [Nature Communications] |
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| Scientists introduced a novel strategy for the generation of prevascularized islet organoids by the fusion of pancreatic islet cells with functional native microvessels. [EMBO Molecular Medicine] |
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| The authors performed an in vivo CRISPR screen in an orthotopic patient-derived xenograft model to identify gene targets whose inhibition created synergistic tumor growth inhibition with gemcitabine. [Proceedings of the National Academy of Sciences of the United States of America] |
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| Investigators present a microfluidic continuous-flow electrotransfection device designed for precise, consistent, and high-throughput genetic modification of target cells in cellular therapy manufacturing applications. [Scientific Reports] |
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| Scientists describe the T-cell Optimized for Packaging (TOP) vector for delivering guide RNAs and transgenes into primary T cells [Molecular Therapy-Methods & Clinical Development] |
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| Scientists provide an overview of the current clinical status of CAR-T and oncolytic virus (OV) therapies. While preclinical studies have demonstrated curative potential, the benefit of CAR-T and OVs as single agent treatments remains limited to a subset of patients. [Molecular Therapy] |
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| The authors focus on the recent findings concerning the roles of immune checkpoint molecules and receptors in the regulation of NK cell function, as well as their potential application in tumor immunotherapy. [Signal Transduction and Targeted Therapy] |
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| EdiGene, Inc. announced the Center for Drug Evaluation of China National Medical Products Administration has accepted for review the company’s Investigational New Drug application for ET-01, autologous CD34+ hematopoietic stem/progenitor cells with the erythroid -specific enhancer of the BCL11A gene modified by CRISPR/Cas9, an investigational gene-editing therapy for patients with transfusion dependent β-thalassemia. [EdiGene, Inc.] |
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| AgeX Therapeutics, Inc. and ImStem Biotechnology, Inc. announced that ImStem has obtained from AgeX a non-exclusive, royalty-bearing sublicense to use AgeX’s clinical-grade ESC line ESI-053 to derive ImStem’s investigational MSC product candidate IMS001 for development in COVID-19 as well as acute respiratory distress syndrome from other causes. [AgeX Therapeutics] |
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| April 11 – April 13, 2021 San Diego, California, United States |
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| EnaraBio – Oxford, England, United Kingdom |
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| LMU University Hospital Munich – Munich, Germany |
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| GlaxoSmithKline – Stevenage, United Kingdom |
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| Nanyang Technological University – Singapore, Singapore |
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| University of Luxembourg- Luxembourg, Luxembourg |
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