Journal article

EphA3 as a target for antibody immunotherapy in acute lymphoblastic leukemia

S Charmsaz, F Al-Ejeh, TM Yeadon, KJ Miller, FM Smith, BW Stringer, AS Moore, FT Lee, LT Cooper, C Stylianou, GT Yarranton, J Woronicz, AM Scott, M Lackmann, AW Boyd

Leukemia | NATURE PUBLISHING GROUP | Published : 2017

Abstract

The human EphA3 gene was discovered in a pre-B acute lymphoblastic leukemia (pre-B-ALL) using the EphA3-specific monoclonal antibody (mAb), IIIA4, which binds and activates both human and mouse EphA3. We use two models of human pre-B-ALL to examine EphA3 function, demonstrating effects on pre-B-cell receptor signaling. In therapeutic targeting studies, we demonstrated antitumor effects of the IIIA4 mAb in EphA3-expressing leukemic xenografts and no antitumor effect in the xenografts with no EphA3 expression providing evidence that EphA3 is a functional therapeutic target in pre-B-ALL. Here we show that the therapeutic effect of the anti-EphA3 antibody was greatly enhanced by adding an α-part..

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University of Melbourne Researchers

Grants

Awarded by ARC


Awarded by Australian Research Council


Funding Acknowledgements

We acknowledge members of the QIMR-Berghofer flow cytometry and Animal facility. We acknowledge funding from Leukaemia Foundation and The Rio Tinto Ride To Conquer Cancer. We thank patients who contributed to the Queensland Children's Tumor Bank. FA is supported by Future Fellowship from the ARC (ID:FT130101417). AMS is supported by an NHMRC fellowship and the Operational Infrastructure Support Scheme, Victorian Government.