hard collection since patients’ status sometimes and weak anti-tumor efficacy since suppression by tumor burden.
NK cells undergoing complete in vivo development and functional maturation and extensive donor/recipient pairing; potent anti-tumor efficacy; suitable for “off-the-shelf” production.
homogeneity and easier genetic manipulation and “off-the-shelf” production; immature functionality (lack of entire NK receptor array such as without CD16, KIR and donor/recipient pairing); potential of malignant transformation.
higher in-vivo proliferation, high NK cell concentration (15–30%); immature NK cells with lower cytotoxicity.
derived from a patient with NK lymphoma; need for irradiation before infusion; limited in vivo activity; safety concern due to tumorigenicity.
Phenotype | PB-NK | iPSC-NK |
KIRs/NKRs(Recognizing tumor) | + + + + | + |
CD16 (ADCC effect) | + + + + | + |
CD62L(Immigration to tumor sites) | + + + + | + |
Mostly autologous cells
High cost in manufacturing
Potential toxicity (CRS and neurotoxicity)
must be hospitalized with ICU support
A variety of allogeneic cell sources
Low cost in manufacturing
Without hospitalization owing to the lack of CRS and/or neurotoxicity
off-the-shelf’ products for multiple outpatients
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