| Vol. 21.37 – 26 October, 2020 |
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| Investigators generated GD2-specific chimeric antigen receptor T lymphocytes and locally delivered them to mice with an in situ grafting retinoblastoma. [Nature Cancer] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| The assessment included incidence of biopsy confirmed acute rejection, assessment of nTreg infusion related adverse effects, and signs of over immunosuppression. [British Medical Journal] |
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| Researchers describe a method to generate oligodendrocyte precursor cells from human pluripotent stem cells in only ~20 days, which could subsequently myelinate neurons, both in vitro and in vivo. [Nature Protocols] |
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| Using a novel Galc floxed allele, investigators induced ubiquitous galactosylceramidase (GALC) ablation at various postnatal timepoints and identified a critical period of vulnerability to GALC ablation between P4-6 in mice. [Nature Communications] |
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| Scientists profiled microglia differentiated from isogenic, CRISPR-modified TREM2-knockout induced pluripotent stem cell lines. [Nature Communications] |
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| By using a high-throughput CRISPR/Cas9-based genetic screen in HepG2 hepatocellular carcinoma cells to search for metabolic proteins inhibiting ferroptosis, researchers identified a branched-chain amino acid aminotransferase 2 as a novel suppressor of ferroptosis. [Cell Death & Differentiation] |
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| Host rejection driven by HLA disparity in adoptively transferred allogeneic T cells remains a key obstacle to the universal donor T cell therapy. To evade donor HLA-mediated immune rejection, scientists attempted to eliminate T cell’s HLA through the CRISPR/Cas9 gene editing system. [Scientific Reports] |
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| Researchers established a novel qPCR methodology incorporating a spike-in calibration curve that expressed cellular kinetics in units of copies/μL blood, as is the case for conventional pharmacokinetic studies of small molecules and other biologics. [Scientific Reports] |
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| Scientists found that the T cell subsets and inflammatory molecules were not affected by mesenchymal stem cell treatment during the follow-up period. In control patients, a significant decrease was detected only at the Th2 subset, TGF-β1, PGE2, IDO and anti-FcεRI levels on the 14th day of treatment. [Stem Cell Reviews and Reports] |
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| Knockdown of CASZ1b via RNA interference increased the expression levels of the aldosterone-induced mineralocorticoid receptor target genes epithelial Na+ channel-α and serum/glucocorticoid regulated kinase 1 by approximately twofold and 2.3-fold. [Hypertension Research] |
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| Gene correction using CRISPR-Cas9 is an extension of gene therapy that has received considerable attention in recent years and boasts many possible uses beyond classical gene therapy approaches. [Gene Therapy] |
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| The authors discuss the anatomical and functional benefit of grafted iPSC-progenitors over their brain counterparts, their use in disease modeling and the missing gaps that still prevent to study their biology in the most integrated way, and to translate iPSC-stem cell based therapy to the clinic. [Seminars in Cell & Developmental Biology] |
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| Bayer AG announced the acquisition of Asklepios BioPharmaceutical, Inc., a US-headquartered biopharmaceutical company specialized in the research, development and manufacturing of gene therapies across different therapeutic areas. [Asklepios BioPharmaceutical] |
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| Global Stem Cells Group (GSCG) has signed a historic agreement with a company known as Bioscience Cell Factor- this Dubai-based healthcare company will allow GSCG to act as their representatives operating in both the Middle East and Latin America. [Global Stem Cells Group] |
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| April 9 – April 14, 2021 Washington, DC, United States |
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| GlaxoSmithKline – Stevenage, England, United Kingdom |
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| H. Lee Moffitt Cancer Center & Research Institute – Tampa, Florida, United States |
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| University of Luxembourg- Luxembourg, Luxembourg |
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| Nanyang Technological University – Singapore, Singapore |
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| Terasaki Research Institute – Los Angeles, California, United States |
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