Targeted therapies in hematological malignancies using therapeutic monoclonal antibodies against Eph family receptors

Exp Hematol. 2017 Oct:54:31-39. doi: 10.1016/j.exphem.2017.07.003. Epub 2017 Jul 24.

Abstract

The use of monoclonal antibodies (mAbs) and molecules derived from them has achieved considerable attention and success in recent years, establishing this mode of therapy as an important therapeutic strategy in many cancers, in particular hematological tumors. mAbs recognize cell surface antigens expressed on target cells and mediate their function through various mechanisms such as antibody-dependent cellular cytotoxicity, complement-dependent cytotoxicity, or immune system modulation. The efficacy of mAb therapy can be improved when they are conjugated to a highly potent payloads, including cytotoxic drugs and radiolabeled isotopes. The Eph family of proteins has received considerable attention in recent years as therapeutic targets for treatment of both solid and hematological cancers. High expression of Eph receptors on cancer cells compared with low expression levels in normal adult tissues makes them an attractive candidate for cancer immunotherapy. In this review, we detail the modes of action of antibody-based therapies with a focus on the Eph family of proteins as potential targets for therapy in hematological malignancies.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / biosynthesis
  • Antibodies, Monoclonal / therapeutic use*
  • Antibody-Dependent Cell Cytotoxicity / drug effects
  • Antineoplastic Agents / therapeutic use
  • Complement Activation / drug effects
  • Cytotoxins / chemistry
  • Cytotoxins / therapeutic use
  • Gene Expression Regulation, Neoplastic*
  • Hematologic Neoplasms / drug therapy*
  • Hematologic Neoplasms / genetics
  • Hematologic Neoplasms / immunology
  • Hematologic Neoplasms / pathology
  • Humans
  • Immunoconjugates / chemistry
  • Immunoconjugates / therapeutic use
  • Immunomodulation / drug effects
  • Immunotherapy / methods
  • Molecular Targeted Therapy*
  • Neoplasm Proteins / antagonists & inhibitors*
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / immunology
  • Receptors, Eph Family / antagonists & inhibitors*
  • Receptors, Eph Family / genetics
  • Receptors, Eph Family / immunology

Substances

  • Antibodies, Monoclonal
  • Antineoplastic Agents
  • Cytotoxins
  • Immunoconjugates
  • Neoplasm Proteins
  • Receptors, Eph Family