Acute myeloid leukemia targets for bispecific antibodies. Review uri icon

Overview

abstract

  • Despite substantial gains in our understanding of the genomics of acute myelogenous leukemia (AML), patient survival remains unsatisfactory especially among the older age group. T cell-based therapy of lymphoblastic leukemia is rapidly advancing; however, its application in AML is still lagging behind. Bispecific antibodies can redirect polyclonal effector cells to engage chosen targets on leukemia blasts. When the effector cells are natural-killer cells, both antibody-dependent and antibody-independent mechanisms could be exploited. When the effectors are T cells, direct tumor cytotoxicity can be engaged followed by a potential vaccination effect. In this review, we summarize the AML-associated tumor targets and the bispecific antibodies that have been studied. The potentials and limitations of each of these systems will be discussed.

publication date

  • February 3, 2017

Research

keywords

  • Antibodies, Bispecific
  • Leukemia, Myeloid, Acute
  • Sialic Acid Binding Ig-like Lectin 3

Identity

PubMed Central ID

  • PMC5386336

Scopus Document Identifier

  • 85011562259

Digital Object Identifier (DOI)

  • 10.1038/bcj.2017.2

PubMed ID

  • 28157217

Additional Document Info

volume

  • 7

issue

  • 2