A diphtheria toxin interleukin-3 fusion protein synergizes with tyrosine kinase inhibitors in killing leukemic progenitors from BCR/ABL positive acute leukemia

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• 作者：Hyun Pyo Kim ; Arthur E. Frankel ; Donna E. Hogge
• 关键词：Ph⁺ acute leukemia ; BCR/ABL ; IL-3 receptor ; Imatinib ; Dasatinib ; DT₃₈₈IL3
• 刊名：Leukemia Research
• 出版年：2010
• 出版时间：August 2010
• 年：2010
• 卷：34
• 期：8
• 页码：1035-1042
• 全文大小：308 K

文摘

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 (DT₃₈₈IL3) 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 DT₃₈₈IL3 correlated with the level of IL-3Rα subunit by FACS. DT₃₈₈IL3 synergized with both imatinib and dasatinib for killing of malignant CFCs. Long-term suspension culture-initiating cells (SC-ICs) and quiescent leukemic cells (G₀ in cell cycle) also were studied and synergistic interactions were again demonstrated. Thus, cotreatment with TKIs and DT₃₈₈IL3 is much more effective in eliminating Ph⁺ leukemic progenitors that express IL-3R than either agent alone.