bioRxivSynthetic BiologyPreprint
Ultra-high efficiency T cell reprogramming at multiple loci with SEED-Selection
Christopher R. ChangiD, Vivasvan S. VykuntaiD, Daniel Bryan GoodmaniD, Joseph J. MuldooniD, William A. NybergiD, Chang LiuiD, Vincent AllainiD, Allison Grace RothrockiD, Charlotte H. WangiD, Alexander MarsoniD, Brian Rudolph ShyiD, Justin EyquemiD
Abstract
Multiplexed reprogramming of T cell specificity and function can generate powerful next-generation cellular therapies. However, current manufacturing methods produce heterogenous mixtures of partially engineered cells. Here, we develop a one-step process to enrich for unlabeled cells with knock-ins at multiple target loci using a family of repair templates named Synthetic Exon/Expression Disruptors (SEEDs). SEED engineering associates transgene integration with the disruption of a paired endogenous surface protein, allowing non-modified and partially edited cells to be immunomagnetically depleted (SEED-Selection). We design SEEDs to fully reprogram three critical loci encoding T cell specificity, co-receptor expression, and MHC expression, with up to 98% purity after selection for individual modifications and up to 90% purity for six simultaneous edits (three knock-ins and three knockouts). These methods are simple, compatible with existing clinical manufacturing workflows, and can be readily adapted to other loci to facilitate production of complex gene-edited cell therapies.
- organism: human
- assay: CRISPR screen
- research focus: gene regulatory network inference
- research focus: variant calling
- research focus: drug response / drug discovery
- approach: experimental assay
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Rapid discovery of synthetic DNA sequences to rewrite endogenous T cell circuits
T. L. Roth, P. J. Li, … A. Marson·bioRxiv·Apr 12, 2019
- A Singular Base Editing Platform for Polyfunctional Multiplex Engineering of Immune Cells
Joseph G. Skeate, Nicholas J. Slipek, … Beau R. Webber·Molecular TherapyPeer-reviewed·Jul 18, 2026
- Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors
Beau R. Webber, Cara-lin Lonetree, … Branden S. Moriarity·Nature CommunicationsPeer-reviewed·Nov 19, 2019
- Programming T cells for intercellular genome editing
Kevin M. Wasko, Madeleine Maker, … Jennifer A. Doudna·bioRxiv·Jun 23, 2026
- Repurposing base editors for targeted knock-in and simultaneous knockouts to generate multiplex-edited allogeneic CAR T cells with minimal translocations
Viktor Glaser, Lily Jo Becker, … Dimitrios L. Wagner·bioRxiv·Sep 15, 2025
- Protocol for Non-viral HDR-based CRISPR/Cas9 platform for small custom editing in primary T cells
Katariina Mamia, Anniken Solveig Matheson Sollano, … Emma Maria Haapaniemi·Frontiers in Genome EditingPeer-reviewed·Sep 30, 2026