686 Mechanism of action of LAVA-051, a bispecific Vγ9Vδ2 T-cell engager (bsTCE), confirmed in the clinical setting

Roeland Lameris, J. Ruben, R. Roovers, A. Kater, T. Riedl, V. Iglesias, A. Broijl, I. Tuinhof, S. Umarale, Anton E P Adang, T. D. Gruijl, P. Parren, B. Winograd, H. V. Vliet
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Abstract

Background LAVA-051, a CD1d-targeting first-in-class bispecific single domain antibody (27 kDa), was brought into the clinic based on its high potency antitumor activity through dual engagement of V g 9V d 2-T and iNKT cells, and a low risk of cytokine release syndrome (CRS). Methods A phase 1 study using LAVA-051 is ongoing in patients with relapsed/refractory MM or CLL to determine the recommended phase 2 dose (RP2D). This study has been approved by relevant ethics committees (NCT04887259). A panel of specific pharmacodynamic assays is included to determine the pattern of change in the binding of LAVA-051 to patients ’ peripheral blood V g 9V d 2-T cells (i.e. V g 9V d 2-TCR occupancy) and in the frequency and activation status of V g 9V d 2-T and iNKT cells in circulation. Data presented are focused on the comparison of clinical to pre-clinical observations. Results LAVA-051 triggers V g 9V d 2-T and iNKT cell mediated pro-inflammatory cytokine production, proliferation and antitumor activity in in vitro and ex vivo assays
686双特异性Vγ9Vδ2 t细胞接合剂(bsTCE) LAVA-051的作用机制在临床环境中得到证实
LAVA-051是一种靶向cd1的一流双特异性单域抗体(27 kDa),由于其通过双重作用于vg9vd2 -t和iNKT细胞而具有高效的抗肿瘤活性,并且具有低风险的细胞因子释放综合征(CRS)而被引入临床。方法使用LAVA-051在复发/难治性MM或CLL患者中进行的1期研究,以确定推荐的2期剂量(RP2D)。本研究已获得相关伦理委员会批准(NCT04887259)。包括一组特定的药效学分析,以确定LAVA-051与患者外周血vg9vd2 - t细胞结合的变化模式(即vg9vd2 - tcr占用),以及循环中vg9vd2 - t和iNKT细胞的频率和激活状态。所提供的数据集中于临床与临床前观察的比较。结果在体外和离体实验中,LAVA-051可触发vg9vd2 - t和iNKT细胞介导的促炎细胞因子的产生、增殖和抗肿瘤活性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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