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February 21, 2026Cell Reports Medicine0 citationsOpen Access

Targeting BCMA in multiple myeloma with a trifunctional NK cell engager

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ATAlexandre TangLGLaurent GauthierEZElisa Zaghi

Key Points

  • This research aims to evaluate the efficacy of SAR445514, a trifunctional NK cell engager, against multiple myeloma.
  • Investigated various molecular formats of NK cell engagers targeting BCMA and NKp46
  • Selected SAR445514 based on its monovalent format for improved antibody-dependent cellular cytotoxicity
  • Conducted in vitro and in vivo experiments to assess anti-tumor activity
  • Performed ex vivo assays using NK cells from multiple myeloma patients
  • SAR445514 exhibited potent anti-tumor activity in both in vitro and in vivo settings
  • Showed enhanced antibody-dependent cellular cytotoxicity compared to other immune cell engagers
  • Induced minimal cytokine release, demonstrating a safer profile compared to T cell therapies
  • Effectively activated NK cells from multiple myeloma patients, leading to cytotoxicity against resistant malignant cells

Abstract

Multiple myeloma (MM), the second most common hematologic malignancy, remains incurable, highlighting the need for durable therapies. Natural killer (NK) cell engagers (NKCEs) represent a promising alternative to T cell therapies, offering potent anti-tumor activity with limited cytokine release. SAR445514 (SAR'514) is a trifunctional NKCE that co-engages NKp46 and FcγRIIIa to activate NK cells while targeting B cell maturation antigen (BCMA) on MM cells. After exploring several molecular formats with varied BCMA and NKp46 valency, we selected SAR'514, a monovalent format with enhanced antibody-dependent cellular cytotoxicity (ADCC). SAR'514 has potent and selective anti-tumor activity in vitro and in vivo, outperforming other FcγRIIIa-immune cell engagers, while inducing minimal cytokine release compared to T cell engagers targeting the same antigen. Ex vivo, SAR'514 efficiently activates NK cells from MM patients and induces cytotoxicity against autologous malignant cells, including those resistant to standard therapies. These findings support further development of SAR'514.

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Cite This Study

Tang et al. (2026) studied this question.

synapsesocial.com/papers/69994a7f873532290d01ee75https://doi.org/10.1016/j.xcrm.2026.102628
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