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Updated: Feb 11, 2026

Transfecting and Nucleofecting Human Induced Pluripotent Stem Cells
Published on: October 5, 2011
Abstract:
Within the field of allogeneic chimeric antigen receptor T-cell therapy, La Jolla, CA-based Fate Therapeutics is exploring in vitro differentiation of induced pluripotent stem cells, rather than T cells harvested from donors, as their source material. Preclinical data on the company's off-the-shelf candidate, FT819, look promising so far.
Insights
Fate Therapeutics is advancing allogeneic chimeric antigen receptor T-cell therapy using induced pluripotent stem cells. Their off-the-shelf candidate, FT819, shows promising preclinical results for cancer treatment.
Area of Science:
- Oncology
- Immunotherapy
- Stem Cell Biology
Background:
- Allogeneic chimeric antigen receptor (CAR) T-cell therapy offers a potential alternative to autologous treatments.
- Current allogeneic CAR T-cell approaches face challenges related to source material and manufacturing.
- Induced pluripotent stem cells (iPSCs) present a novel source for generating CAR T-cells.
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