| Literature DB >> 24723681 |
Leonid Dubrovsky1, Dmitry Pankov2, Elliott Joseph Brea3, Tao Dao4, Andrew Scott4, Su Yan5, Richard J O'Reilly6, Cheng Liu5, David A Scheinberg3.
Abstract
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 IgG1 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, T315I. 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.Entities:
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Year: 2014 PMID: 24723681 PMCID: PMC4046427 DOI: 10.1182/blood-2014-01-549022
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113