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EphA3 as a target for antibody immunotherapy in acute lymphoblastic leukemia

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posted on 2023-02-03, 01:09 authored by S Charmsaz, F Al-Ejeh, TM Yeadon, KJ Miller, FM Smith, BW Stringer, AS Moore, Fook-Thean LeeFook-Thean Lee, LT Cooper, C Stylianou, GT Yarranton, J Woronicz, Andrew ScottAndrew Scott, M Lackmann, AW Boyd
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-particle-emitting 213 Bismuth payload.

Funding

We acknowledge funding from Leukaemia Foundation and The Rio Tinto Ride To Conquer Cancer. 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.

History

Publication Date

2017-08-01

Journal

Leukemia

Volume

31

Issue

8

Pagination

9p. (p. 1779-1787)

Publisher

Nature

ISSN

0887-6924

Rights Statement

© The Author(s) 2017 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/