Guiding the Killer and Bringing in Accomplices: Bispecific Antibody Treatment for Malignant Melanoma

J Invest Dermatol. 2016 Feb;136(2):362-364. doi: 10.1016/j.jid.2015.12.002.

Abstract

Discovery of oncogene and immune checkpoint targeting has transformed melanoma therapy in the last 5 years. However, treatment of primary or secondary drug-resistant melanoma remains a challenge. Agents designed to activate the cell death machinery directly, for example by activating the death receptors expressed by melanoma cells, could break drug resistance, and they may achieve long-lasting therapeutic success. He et al. report their studies of an MCSPxDR5 bispecific, tetravalent antibody that can simultaneously target death receptor 5 (DR5, TRAIL-R2) and melanoma-associated chondroitin sulfate proteoglycan (MCSP). This antibody can exert strong and selective DR5-dependent cytotoxic activity against MCSP-expressing melanoma cells. Crosslinking of the antibody with Fcγ-receptors increased the cytotoxic potential further, without compromising its selectivity. This approach offers a novel immunotherapeutic tool via coupling of three cooperating processes: delivering the death receptor agonist to the malignant cell population, potent activation of DR5-mediated cell death signaling, and recruitment of Fcγ-receptor-carrying immune cells that can mount an immune response against the tumor cells.

Publication types

  • Comment

MeSH terms

  • Apoptosis / immunology*
  • Humans
  • Mitochondrial Proteins / immunology*
  • Receptors, TNF-Related Apoptosis-Inducing Ligand / immunology*

Substances

  • Mitochondrial Proteins
  • Receptors, TNF-Related Apoptosis-Inducing Ligand