Fig. 1.
Fig. 1. NK92 cells transduced with p210 become IL-2 independent. / Untransduced (parental) NK92 cells were transduced with a control vector (eGFP) and a vector containing BCR/ABL (p210). Parental and sorted eGFP+ (termed eGFP) and p210-eGFP+ NK92 cells (termed p210+) (3 × 105 cells/mL) were cultured in the presence (▨) or absence (▪) of 500 U/mL IL-2, and the number of viable cells was determined after 14 days of culture. Parental and eGFP+control NK92 cells died in the absence of IL-2, whereas p210+ cells without IL-2 expanded at similar rates as parental NK92 cells in the presence of IL-2.

NK92 cells transduced with p210 become IL-2 independent.

Untransduced (parental) NK92 cells were transduced with a control vector (eGFP) and a vector containing BCR/ABL (p210). Parental and sorted eGFP+ (termed eGFP) and p210-eGFP+ NK92 cells (termed p210+) (3 × 105 cells/mL) were cultured in the presence (▨) or absence (▪) of 500 U/mL IL-2, and the number of viable cells was determined after 14 days of culture. Parental and eGFP+control NK92 cells died in the absence of IL-2, whereas p210+ cells without IL-2 expanded at similar rates as parental NK92 cells in the presence of IL-2.

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