At the heart of Cellistic’s mission is the commitment to making cell therapy globally accessible by leveraging the significant advantages of iPSCs. The Allo Chassis™ cell lines embody this vision, giving therapeutic developers a novel resource to shorten their development timelines while reducing costs. With ready-to-use, immune-cloaked CD34+ and CD4+ T-cell derived iPSC cell lines, this new offering paves the way for faster market-ready therapies, ultimately improving patient access to essential treatments.
Innovation enabled by proprietary STAR-CRISPR™ gene editing technology
The Allo Chassis™ cell lines are immediately available, off-the-shelf resources edited using Cellistic’s proprietary STAR-CRISPR™ gene editing technology. This provides partners access to advanced gene editing capabilities with a clear intellectual property licensing route to commercialization. The cGMP Allo Chassis™ cell banks are produced with validated workflows, rigorous quality control, and state-of-the-art automation to ensure the delivery of high-quality, low-passage cell lines ready for therapeutic use.
“Allo Chassis™ provides therapeutic developers with iPSC starting material featuring the most commonly used gene modifications, resulting in the deletion of HLA class I and II. These off-the-shelf cell lines can be efficiently customized using our STAR-CRISPR™ gene editing technology, enabling rapid creation of product-specific master cell banks at a significantly reduced cost.” says Stefan Braam, Founder and CTO of Cellistic.
The Allo Chassis™ CD34+ and CD4+ T-cell derived immune-cloaked cell banks are immediately available for researchers and developers. With this innovative product, Cellistic reaffirms its commitment to supporting therapeutic developers with integrated, iPSC-based solutions for producing advanced cell therapies.
About Cellistic®
Cellistic specializes in the process development and manufacturing of immune cell therapies based on human induced pluripotent stem cell (iPSC) technology, using their Pulse™ and Echo™ Platform. Its focus and expertise in iPSC reprogramming, gene editing using its proprietary STAR-CRISPR™ technology ,and differentiation development, positions the company to be the partner of choice for innovative cell therapy developers to advance into clinic. Leveraging more than a decade of scientific and technical knowledge and experience, Cellistic possesses unique capabilities for the design and optimization of proprietary manufacturing platforms for iPSC- based cell therapies.