| Literature DB >> 25413948 |
Nenad Tomasevic1, Kenneth Luehrsen, Mark Baer, Varghese Palath, David Martinez, Jason Williams, Christina Yi, Swathi Sujatha-Bhaskar, Rohini Lanke, John Leung, Wendy Ching, Andreia Lee, Lu Bai, Geoffrey Yarranton, Christopher Bebbington.
Abstract
EphA3 is expressed in solid tumors and leukemias and is an attractive target for the therapy. We have generated a panel of Humaneered® antibodies to the ligand-binding domain using a Fab epitope-focused library that has the same specificity as monoclonal antibody mIIIA4. A high-affinity antibody was selected that competes with the mIIIA4 antibody for binding to EphA3 and has an improved affinity of ∼1 nM. In order to generate an antibody with potent cell-killing activity the variable regions were assembled with human IgG1k constant regions and expressed in a Chinese hamster ovary (CHO) cell line deficient in fucosyl transferase. Non-fucosylated antibodies have been reported to have enhanced binding affinity for the IgG receptor CD16a (FcγRIIIa). The affinity of the antibody for recombinant CD16a was enhanced approximately 10-fold. This resulted in enhanced antibody-dependent cell-mediated cytotoxicity (ADCC) activity against EphA3-expressing leukemic cells, providing a potent antibody for the evaluation as a therapeutic agent.Entities:
Keywords: ADCC; EphA3; Humaneered; leukemia; non-fucosylated
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Year: 2014 PMID: 25413948 DOI: 10.3109/08977194.2014.984808
Source DB: PubMed Journal: Growth Factors ISSN: 0897-7194 Impact factor: 2.511