优化一种新型 2 + 2 BCMA × CD3 双特异性抗体以实现最小化细胞因子释放和强效疗效

Cytokine release syndrome remains a critical challenge for clinical use of bispecific T-cell engagers.

We present the preclinical development of a novel B-cell maturation antigen × CD3 bispecific antibody with the aim of reducing cytokine release while maintaining potent efficacy in the treatment of multiple myeloma. Based on the Fabs-in-tandem (FIT) geometry, bispecific molecules with two target arms in cis-configuration were constructed. A panel of anti-CD3 mAbs with varying affinities was generated, and the impact of binding arm geometry, valency, and anti-CD3 affinity on the T-cell engager's safety and efficacy profile was evaluated both in vitro and in vivo.

By comparing with different formats, including a reference tandem scFv, we show that both binding arm valency and CD3 affinity determine redirected T-cell cytotoxicity in vitro. The FIT-Ig with 2 + 2 binding valencies and medium CD3 affinity (CD3med FIT-Ig) can achieve the same potent antitumor activity as the reference tandem scFv, but it induced much less cytokine release.

Importantly, bivalent CD3 binding does not introduce target-irrelevant T-cell activation in the FIT-Ig format. The low cytokine release profile of the CD3med FIT-Ig was further validated in human peripheral blood mononuclear cells engrafted mice and cynomolgus monkeys. The CD3med FIT-Ig (also known as EMB-06) could offer a differentiated safety profile with effective antitumor activity.