Insights
Echo-T
iPSC-derived T cell manufacturing platform
Echo-T provides a pre-established platform to support the development and GMP manufacturing of iPSC-derived T cell therapies, supporting immune cell therapy programs from concept to clinic.
Cell types
- CD8
- CD4
- CD4/8 DP
- Treg
Platform strengths
- Differentiation protocol
- Industrialized
- Scalable
- Feeder-free
- Chemically defined
Manufacturing services
- Tech transfer
- Process & Analytical Development
- Cell Line Development
- Clinical Manufacturing & QC testing
Why iPSCs offer you a different path to control, consistency, and scale
Donor-derived cell therapy manufacturing — whether autologous or healthy-donor derived — is constrained by variability in starting material, limited scalability, and reduced control over downstream product design. iPSC-derived manufacturing changes that model by starting from a renewable, engineerable cell bank that supports process standardization, defined cell outputs, and industrialized scale-up.
An industrialized process for iPSC-derived T-cell manufacturing
Echo-T follows a controlled manufacturing workflow organized into defined unit operations, from iPSC amplification to final drug product. Built for scalable GMP production, the platform combines feeder-free, chemically defined processing with stirred-tank bioreactors and in-process control across key stages.
- Defined unit operations
- Feeder-free, chemically defined process
- No scale-limiting cell sorting steps
- Stirred-tank bioreactors
- In-process control
Building your product-specific Master Cell Bank with Pulse™
Pulse™, Cellistic's cell line development platform, integrates your CAR or TCR into a defined iPSC line to generate a product-specific, GMP-compliant Master Cell Bank — the foundation Echo-T uses for GMP manufacturing.
- CAR/TCR integration into a defined iPSC line
- STAR-CRISPR™ multiplex gene editing
- GMP-compliant, monoclonal Master Cell Bank
- Direct transition into Echo-T GMP manufacturing
Platform outputs
Cellistic has developed the Echo-T GMP manufacturing platform to fully unlock the potential of allogeneic T-cells.
α/β T cells
Using a single master iPSC line, Echo-T produces CD4 and CD8 T cells at scale in a xeno-free medium. The cells carry no graft-versus-host disease risk, do not lose potency through over-activation during culture, and display functionality similar to primary T-cells — answering the manufacturing challenges currently preventing the widespread use of these therapies.
Download the poster
Tregs
Beyond standard T-cells, the Echo-T platform generates iPSC-derived regulatory T-cells with a stable phenotype and suppressive function comparable to primary Tregs. Cellistic iPSC-derived Tregs introduce a novel option in the management of autoimmune diseases and circumvent current manufacturing challenges.
Download the case study
Built on Cellistic's Echo platform expertise
Echo-T is part of Cellistic's Echo platform family for iPSC differentiation and scalable GMP manufacturing. The platform supports controlled development, clinically relevant manufacturing strategies, and reproducible scale-up across cell therapy programs. It integrates Cellistic's 15+ years of experience in cell therapy and batch release with access to a dedicated GMP manufacturing facility for iPSC-derived cell therapies in Belgium, Europe.
Begin your manufacturing discussion with the Cellistic team.
Get a deeper look at the facility and learn how our dedicated GMP environment can support your program's next steps.
Echo-T is Cellistic's iPSC-derived T-cell therapy manufacturing platform. It provides a pre-established platform to support the development and GMP manufacturing of iPSC-derived T-cell therapies, taking immune cell therapy programs from concept through clinical manufacturing.
Echo-T produces CD8, CD4, CD4/8 double-positive, and Treg cell types from a single iPSC-derived platform.
Echo-T's iPSC-derived CD8 and CD4 T cells can serve as a starting cell type for engineered cell therapy programs, including CAR-T and TCR-T.
Donor-derived manufacturing — whether autologous or healthy-donor allogeneic — is constrained by variability in starting material, limited scalability, and reduced control over downstream product design. Echo-T's iPSC-derived approach starts from a single, renewable, engineerable cell bank, which supports process standardization, defined cell outputs, and industrialized scale-up.
Yes. Echo-T is built on a single master iPSC line, from which CD4 and CD8 T cells are produced at scale in controlled bioreactor conditions, removing reliance on variable donor material for each manufacturing batch.
Yes. Echo-T runs on a feeder-free, defined differentiation and expansion process, without scale-limiting cell sorting steps.
Echo-T platform is optimized for differentiation towards either αβ T cells (CD4, CD8) orTregs, each supported by dedicated phenotypic and functional characterization data.
Echo-T follows a controlled, GMP-ready workflow organized into defined unit operations:
1. iPSC amplification
2. Hemogeneic endothelium
3. HSC (can be cryopreserved)
4. T cell differentiation
5. T cell activation and expansion
6. Automated fill and finish and cryopreservation
7. Drug product release