| Literature DB >> 35001074 |
Satoko Kakiuchi-Kiyota1, Thorsten Ross2, Heidi Ackerly Wallweber1, James R Kiefer1, Melissa M Schutten1, Adeyemi O Adedeji1, Hao Cai1, Robert Hendricks1, Sivan Cohen1, Srividya Myneni1, Luna Liu1, Aaron Fullerton1, Nicholas Corr1, Lanlan Yu1, Denise de Almeida Nagata1, Shelly Zhong1, Steven R Leong1, Ji Li1, Rin Nakamura1, Teiko Sumiyoshi1, Jinze Li1, Ayse Meric Ovacik1, Bing Zheng1, Mike Dillon1, Christoph Spiess1, Susanne Wingert2, Erich Rajkovic2, Kristina Ellwanger2, Uwe Reusch2, Andrew G Polson3.
Abstract
Despite the recent progress, multiple myeloma (MM) is still essentially incurable and there is a need for additional effective treatments with good tolerability. RO7297089 is a novel bispecific BCMA/CD16A-directed innate cell engager (ICE®) designed to induce BCMA+ MM cell lysis through high affinity binding of CD16A and retargeting of NK cell cytotoxicity and macrophage phagocytosis. Unlike conventional antibodies approved in MM, RO7297089 selectively targets CD16A with no binding of other Fcγ receptors, including CD16B on neutrophils, and irrespective of 158V/F polymorphism, and its activity is less affected by competing IgG suggesting activity in the presence of M-protein. Structural analysis revealed this is due to selective interaction with a single residue (Y140) uniquely present in CD16A opposite the Fc binding site. RO7297089 induced tumor cell killing more potently than conventional antibodies (wild-type and Fc-enhanced) and induced lysis of BCMA+ cells at very low effector-to-target ratios. Preclinical toxicology data suggested a favorable safety profile as in vitro cytokine release was minimal and no RO7297089-related mortalities or adverse events were observed in cynomolgus monkeys. These data suggest good tolerability and the potential of RO7297089 to be a novel effective treatment of MM patients.Entities:
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Year: 2022 PMID: 35001074 DOI: 10.1038/s41375-021-01478-w
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528