| Vol. 24.22 – 26 June, 2023 |
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| To explore the use of CAR T cells for the treatment of people with autoimmune disease, and to improve their safety, scientists engineered them with RNA —rather than the conventional DNA approach—to target B cell maturation antigen expressed on plasma cells. [Lancet Neurology] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| The authors engineered nanosized immunofilaments, with a soluble semiflexible polyisocyanopeptide backbone that presented peptide-loaded major histocompatibility complexes and costimulatory molecules multivalently. [ACS Nano] |
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| Investigators showed that Fc receptor-homolog 5 (FcRH5) was expressed on multiple myeloma cells and could be targeted with CAR-T cells. FcRH5 CAR-T cells elicited antigen-specific activation, cytokine secretion, and cytotoxicity against multiple myeloma cells. [Nature Communications] |
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| Researchers identified the transmembrane protein CD317 as a novel target antigen for CAR T cell therapy against glioblastoma, one of the most aggressive solid tumors. [Neuro-Oncology] |
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| Scientists transplanted stem cell–derived retinal pigment epithelial (RPE) into the subretinal space of immunocompetent rabbits for one month and conducted single-cell RNA sequencing analyses on the explanted RPE monolayers. [Proceedings Of The National Academy Of Sciences Of The United States Of America] |
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| Investigators created a new engineered cytokine receptor able to constitutively recreate receptor-heterodimer utilizing the heterodimerization domain derived from the IgG1 antibody. [Cancer Immunology Research] |
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| Using a virus-free and non-transgenic minicircle DNA vector, the authors enabled the rapid generation of CD19 CAR-T cells within two days. [Cancer Letters] |
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| In vivo experiments showed that vitamin A-modified zeolitic imidazolate framework-8 (ZIF-8) lipid nanoparticles could reduce liver injury, improve the degree of liver fibrosis (LF), and exert specific therapeutic effects on LF. [International Journal Of Pharmaceutics] |
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| Scientists established new stem cell-based therapies for treating bone defects by delivering the stem cells sorted from periosteum using flow cytometry within the platelet-rich plasma. [Tissue and Cell] |
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| Investigators present the latest CRISPR-Cas9 technology achievements and prospect to translational medicine advances. [Advanced Science] |
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| Scientists introduce the physiological state of the cervicovaginal cavity and the characteristics of the intravaginal environment in cervical cancers and discuss both “first mucus-adhering then mucosal penetration” and “first mucus-penetrating then mucosal penetration” strategies. [Small] |
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| The authors introduce different design strategies of CAR-T cell delivery hydrogels and discuss various types of therapeutic agents incorporated in the hydrogel platforms and diverse hydrogel formulations. [MedComm] |
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| Sarepta Therapeutics, Inc. announced US FDA accelerated approval of ELEVIDYS, an adeno-associated virus based gene therapy for the treatment of ambulatory pediatric patients aged 4 through 5 years with Duchenne muscular dystrophy (DMD) with a confirmed mutation in the DMD gene. [Sarepta Therapeutics, Inc.] |
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| Partners in the international consortium CAR T-REX announced the awarding of a highly competitive European Innovation Council (EIC) Pathfinder Open grant, following the positive evaluation of their project entitled ‘CAR T Cells Rewired to Prevent EXhaustion in the Tumor Microenvironment’. [Center For Research In Biological Chemistry and Molecular Materials] |
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| July 17 – 20, 2023 Burlington, Vermont, United States |
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| Weill Cornell Medicine – New York, New York, United States |
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| University Hospital RWTH Aachen – Aachen, Germany |
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| University of Gothenburg – Gothenburg, Sweden |
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| VIB Center for Cancer Biology – Leuven, Belgium |
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| Fred Hutchinson Cancer Center – Seattle, Washington, United States |
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