This concept refers to NK cells generated from induced pluripotent stem cells and further improved by genetic modification for anti-cancer immunotherapy. The review frames them as an off-the-shelf-like, controllable source of NK cells.
First-pass extracted concept
engineered iPSC-derived natural killer cells
Aliases
iNK cells, iPSC-derived NK cells
Extracted Explainers
What the tool is doing
Resources required
What problem it solves
What it does not solve
Evidence Snippets
Supporting Sources
Linked Claims
Genetic modification of iPSCs has achieved improvements in cancer targeting, expansion, persistence, and cytotoxic functionality of iPSC-derived NK cells in vitro and in vivo.
Finally, we summarise the improvements in cancer targeting, expansion, persistence and cytotoxic functionality of iPSC-derived NK (iNK) cells both in vitro and in vivo, achieved through genetic modification of iPSCs, as well as recent related clinical trials.
iPSCs are emerging as a controlled and promising inexhaustible source of genetically modifiable NK cells for cell therapies.
Induced pluripotent stem cells (iPSCs) are emerging as a platform to create specific cells with highly controlled processes, allowing for a common cell source for cell therapies and offering a promising inexhaustible source of genetically modifiable NK cells.
Peripheral-blood sourcing of NK cells poses scalability, consistency, and variability challenges.
However, sourcing NK cells from peripheral blood poses challenges in terms of scalability, consistency and variability.
NK cells are potent tumoricidal agents that can be used for cancer immunotherapy.
Natural killer (NK) cells are increasingly recognised as potent tumoricidal agents that can be utilised for cancer immunotherapy.
Recent developments include generating iPSC-derived NK cells in defined culture systems and genetically modifying them to improve iPSC-NK cell therapy.
This review highlights recent developments in the field of generating iPSC-derived NK cells in defined culture systems, and advancements in genetic modification to improve iPSC-NK cell therapy.