Abstract
Despite initial remissions, most patients with Ph chromosome positive (Ph +) acute leukemia (AL) become refractory to tyrosine kinase inhibitors (TKIs) such as imatinib and dasatinib. This study was designed to determine if targeting the interleukin-3 receptor (IL-3R) with a diphtheria toxin fusion protein (DT 388IL3) would improve the effectiveness of TKIs against Ph + AL cells. IL-3R subunits were detected on most Ph + cells and the IC50 for killing of colony forming cell (CFC) with DT 388IL3 correlated with the level of IL-3Rα subunit by FACS. DT 388IL3 synergized with both imatinib and dasatinib for killing of malignant CFCs. Long-term suspension culture-initiating cells (SC-ICs) and quiescent leukemic cells (G 0 in cell cycle) also were studied and synergistic interactions were again demonstrated. Thus, cotreatment with TKIs and DT 388IL3 is much more effective in eliminating Ph + leukemic progenitors that express IL-3R than either agent alone.
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