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EphA3 as a target for antibody immunotherapy in acute lymphoblastic leukemia

  • Sara Charmsaz
  • , Fares Al-Ejeh
  • , T. M. Yeadon
  • , K. J. Miller
  • , Florentia M Smith
  • , Brett William Stringer
  • , A. S. Moore
  • , F. T. Lee
  • , L. T. Cooper
  • , Con Stylianou
  • , Geoff T. Yarranton
  • , J. Woronicz
  • , A. M. Scott
  • , M. Lackmann
  • , A. W. Boyd

Research output: Contribution to journalArticleResearchpeer-review

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-particle-emitting 213 Bismuth payload.

Original languageEnglish
Pages (from-to)1779-1787
Number of pages9
JournalLeukemia
Volume31
Issue number8
DOIs
Publication statusPublished - 1 Aug 2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • acute lymphocytic leukaemia
  • preclinical research

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