Figure 2.
Figure 2. Dinaciclib enhances NK-cell killing of leukemic target cells in human AML cell line xenograft mice. NSG mice were conditioned, engrafted with luciferase-expressing HL60 AML cells, and then treated with dinaciclib and/or enriched primary human NK cells from healthy donors as outlined (A). Mice that received human NK cells also received 5 µg of recombinant human IL15 (rhIL15) 3 times per week. Leukemic burden was analyzed by bioluminescent imaging (B) and peripheral blood was obtained to enumerate human NK-cell numbers (human CD45+CD3−CD56+ cells) (C) at 28 days after NK-cell injection. Error bars represent mean ± standard error of the mean. *P < .05 using a paired Student t test corrected for multiple comparisons. IP, intraperitoneally; n.s., nonsignificant P value.

Dinaciclib enhances NK-cell killing of leukemic target cells in human AML cell line xenograft mice. NSG mice were conditioned, engrafted with luciferase-expressing HL60 AML cells, and then treated with dinaciclib and/or enriched primary human NK cells from healthy donors as outlined (A). Mice that received human NK cells also received 5 µg of recombinant human IL15 (rhIL15) 3 times per week. Leukemic burden was analyzed by bioluminescent imaging (B) and peripheral blood was obtained to enumerate human NK-cell numbers (human CD45+CD3CD56+ cells) (C) at 28 days after NK-cell injection. Error bars represent mean ± standard error of the mean. *P < .05 using a paired Student t test corrected for multiple comparisons. IP, intraperitoneally; n.s., nonsignificant P value.

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