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Updated: Jul 8, 2026

Non-Viral Engineering of Primary Human T Cells via Homology-Mediated End-Joining Targeted Integration of Large DNA Templates
Published on: May 9, 2025
Fundamentals of engineered T cell therapies: From basic design to bells and whistles
Janna C Minehart1, Eric W Cross2, Praise S Oo3
1Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States; Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Abstract:
T cells endowed with defined antigen specificity by provision of monoclonal T cell receptors (TCR) or synthetic Chimeric Antigen Receptors (CAR) have established themselves as a potent drug class with several such products now commercially available. This review addresses fundamental aspects of the design of engineered TCR and CAR T therapies. Beyond the basic design features, we touch upon several additional strategies that have been developed or are currently in pre-clinical development to enhance the efficacy or safety of such therapies. Within the vast and quickly growing space of T cell engineering, this discussion is not all-encompassing but aims to lay a foundation for other reviews in the series that delve into more focused aspects of T cell therapy.

