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

Research output: Contribution to a Journal (Peer & Non Peer)Editorial

5 Citations (Scopus)

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 Fc gamma-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 Fc gamma-receptor-carrying immune cells that can mount an immune response against the tumor cells.
Original languageEnglish (Ireland)
Pages (from-to)362-364
Number of pages3
JournalJOURNAL OF INVESTIGATIVE DERMATOLOGY
Volume136
Issue number2
DOIs
Publication statusPublished - 1 Feb 2016

Authors (Note for portal: view the doc link for the full list of authors)

  • Authors
  • Szegezdi, E,Leverkus, M
  • Eva Szegezdi, Martin Levelrkus

Fingerprint

Dive into the research topics of 'Guiding the Killer and Bringing in Accomplices: Bispecific Antibody Treatment for Malignant Melanoma: Bispecific Antibody Treatment for Malignant Melanoma'. Together they form a unique fingerprint.

Cite this