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 language | English (Ireland) |
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Pages (from-to) | 362-364 |
Number of pages | 3 |
Journal | JOURNAL OF INVESTIGATIVE DERMATOLOGY |
Volume | 136 |
Issue number | 2 |
DOIs | |
Publication status | Published - 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