High quality on-demand gene edited human primary T-cells 2671

Abstract Description EditCo unveils a breakthrough in T-cell engineering: a rapid platform delivering premium-quality edited human CD4+ and CD8+ T-cells with unprecedented efficiency. The platform achieves knock-out efficiency greater than 80% in less than 2 weeks, with edited cell pools maintaining viability above 70% before cryopreservation. These cells can be thawed and expanded at least 30-fold over 14 days independent of TCR stimulation, with no loss in editing efficiency. The platform’s versatility has been demonstrated across multiple unique gene targets and diverse donor populations. Notably, edited CD4+ T-cells retain robust functionality after cryo-recovery, producing IL2, IFNγ, and TNFα upon stimulation. Similarly, edited CD8+ T-cells maintain their endogenous antigen-specific cytotoxic activity, successfully express lentiviral CAR-T constructs, and demonstrate bi-specific engager-mediated cell killing. This comprehensive validation establishes EditCo’s platform as a versatile, high-performance solution for T-cell editing, maintaining cellular integrity and functionality while delivering consistent results across multiple genetic targets and donor populations. Topic Categories Technological Innovations in Immunology (TECH)

Authors

Publication Details

Journal
The Journal of Immunology
Published
2025-11-01
DOI
https://doi.org/10.1093/jimmun/vkaf283.562
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00
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article

High quality on-demand gene edited human primary T-cells 2671

John Latimer, Paolo Piazza, A. Crum Brown
The Journal of Immunology
CAR-T cell therapy research
article

High quality on-demand gene edited human primary T-cells 2671

John Latimer, Paolo Piazza, A. Crum Brown
article en

Abstract

Abstract Description EditCo unveils a breakthrough in T-cell engineering: a rapid platform delivering premium-quality edited human CD4+ and CD8+ T-cells with unprecedented efficiency. The platform achieves knock-out efficiency greater than 80% in less than 2 weeks, with edited cell pools maintaining viability above 70% before cryopreservation. These cells can be thawed and expanded at least 30-fold over 14 days independent of TCR stimulation, with no loss in editing efficiency. The platform’s versatility has been demonstrated across multiple unique gene targets and diverse donor populations. Notably, edited CD4+ T-cells retain robust functionality after cryo-recovery, producing IL2, IFNγ, and TNFα upon stimulation. Similarly, edited CD8+ T-cells maintain their endogenous antigen-specific cytotoxic activity, successfully express lentiviral CAR-T constructs, and demonstrate bi-specific engager-mediated cell killing. This comprehensive validation establishes EditCo’s platform as a versatile, high-performance solution for T-cell editing, maintaining cellular integrity and functionality while delivering consistent results across multiple genetic targets and donor populations. Topic Categories Technological Innovations in Immunology (TECH)

The Journal of ImmunologyVol. 214(Supplement_1)
Openalex Percentile: Top 51%
CAR-T cell therapy research
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High quality on-demand gene edited human primary T-cells 2671 — John Latimer, Paolo Piazza, et al. · The Journal of Immunology (2025) | TGRS Research Map | TGRS