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Development of a Practical GMP-Compliant Manufacturing Process for T Cell-Derived Induced Pluripotent Stem Cells

GMP-compliant iPSC manufacturing has advanced significantly—yet producing clinical-grade cells still demands months of complex work. Published in Cytotherapy (2025), this study tackles that challenge directly.
The authors detail a complete workflow for reprogramming T cells from healthy donor peripheral blood into iPSC, yielding 13 unique lines suitable for clinical applications. The study focuses on standardizing cell enumeration, managing staff and materials efficiently, and reducing batch-to-batch variability. Gene deletions identified across the iPSC lines were independently verified using electronic genome mapping (EGM) on the OhmX™ Platform.


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