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• W4386102384 abstract "Hyper-IgM1 is a rare X-linked combined immunodeficiency caused by mutations in the CD40 ligand (CD40LG) gene with a median survival of 25 years, potentially treatable with in situ CD4+ T cell gene editing with Cas9 and a one-size-fits-most corrective donor template. Here, starting from our research-grade editing protocol, we pursued the development of a good manufacturing practice (GMP)-compliant, scalable process that allows for correction, selection and expansion of edited cells, using an integrase defective lentiviral vector as donor template. After systematic optimization of reagents and conditions we proved maintenance of stem and central memory phenotypes and expression and function of CD40LG in edited healthy donor and patient cells recapitulating the physiological CD40LG regulation. We then documented the preserved fitness of edited cells by xenotransplantation into immunodeficient mice. Finally, we transitioned to large-scale manufacturing, and developed a panel of quality control assays. Overall, our GMP-compliant process takes long-range gene editing one step closer to clinical application with a reassuring safety profile." @default.
• W4386102384 created "2023-08-24" @default.
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• W4386102384 date "2023-09-01" @default.
• W4386102384 modified "2023-10-01" @default.
• W4386102384 title "Scalable GMP compliant gene correction of CD4+ T cells with IDLV template functionally validated in vitro and in vivo" @default.
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• W4386102384 doi "https://doi.org/10.1016/j.omtm.2023.08.020" @default.
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