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A TCR-mimic antibody to WT1 bypasses tyrosine kinase inhibitor resistance in human BCR-ABL~+ leukemias

机译:抗WT1的TCR模拟抗体绕过人BCR-ABL〜+白血病中的酪氨酸激酶抑制剂耐药性

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摘要

Acute and chronic leukemias, including CD34~+ CML cells, demonstrate increased expression of the Wilms tumor gene 1 product (WT1), making WT1 an attractive therapeutic target. However, WT1 is a currently undruggable, intracellular protein. ESKM is a human lgG1 T-cell receptor mimic monoclonal antibody directed to a 9-amino acid sequence of WT1 in the context of cell surface HLA-A*02. ESKM was therapeutically effective, alone and in combination with tyrosine kinase inhibitors (TKIs), against Philadelphia chromosome-positive acute leukemia in murine models, including a leukemia with the most common, pan-TKI, gatekeeper resistance mutation, T3151. ESKM was superior to the first-generation TKI, imatinib. Combination therapy with ESKM and TKIs was superior to either drug alone, capable of curing mice. ESKM showed no toxicity to human HLA-A*02:01~+ stem cells under the conditions of this murine model. These features of ESKM make it a promising nontoxic therapeutic agent for sensitive and resistant Ph~+ leukemias.
机译:急性和慢性白血病,包括CD34〜+ CML细胞,证明Wilms肿瘤基因1产物(WT1)的表达增加,使WT1成为有吸引力的治疗靶标。但是,WT1是目前不可吸收的细胞内蛋白。 ESKM是在细胞表面HLA-A * 02中针对WT1的9个氨基酸序列的人IgG1 T细胞受体模拟单克隆抗体。 ESKM单独或与酪氨酸激酶抑制剂(TKIs)结合使用可有效治疗鼠模型中的费城染色体阳性急性白血病,包括最常见的pan-TKI,关守耐药突变T3151的白血病。 ESKM优于第一代TKI伊马替尼。 ESKM和TKIs的联合疗法优于单独的两种药物,能够治愈小鼠。在该鼠模型的条件下,ESKM对人HLA-A * 02:01〜+干细胞没有毒性。 ESKM的这些特征使其成为用于敏感和耐药性Ph〜+白血病的有前途的无毒治疗剂。

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