Biting back: BiTE antibodies as a promising therapy for acute myeloid leukemia

Expert Rev Hematol. 2014 Jun;7(3):317-9. doi: 10.1586/17474086.2014.896190. Epub 2014 Mar 11.

Abstract

The experience with gemtuzumab ozogamicin has highlighted both the potential value and limitations of antibodies in acute myeloid leukemia (AML). Recently, bispecific T-cell engager (BiTE) antibodies have emerged as a means to harness polyclonal cytotoxic T-cells and cause highly efficient lysis of targeted tumor cells. Promising early results have been obtained with the CD19-directed BiTE antibody, blinatumomab, in patients with acute lymphoblastic leukemia. A first candidate for AML is the CD33/CD3 molecule, AMG 330, for which several recent preclinical studies demonstrated high potency and efficacy in destroying CD33(+) human AML cells. Many questions remain to be addressed, but BiTE antibodies may offer an exciting new tool in a disease for which the outcomes in many patients remain unsatisfactory.

Keywords: AMG 330; acute myeloid leukemia; antibody; bispecific; bite; cd3; cd33; gemtuzumab ozogamicin; immunotherapy.

Publication types

  • Editorial

MeSH terms

  • Antibodies, Bispecific / therapeutic use*
  • Humans
  • Leukemia, Myeloid, Acute / drug therapy*

Substances

  • Antibodies, Bispecific
  • blinatumomab