Molecular Partners AG, Zurich-Schlieren, Switzerland.
Department of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Cancer Immunol Res. 2024 Jul 2;12(7):921-943. doi: 10.1158/2326-6066.CIR-23-0692.
The prognosis of patients with acute myeloid leukemia (AML) is limited, especially for elderly or unfit patients not eligible for hematopoietic stem cell (HSC) transplantation. The disease is driven by leukemic stem cells (LSCs), which are characterized by clonal heterogeneity and resistance to conventional therapy. These cells are therefore believed to be a major cause of progression and relapse. We designed MP0533, a multispecific CD3-engaging designed ankyrin repeat protein (DARPin) that can simultaneously bind to three antigens on AML cells (CD33, CD123, and CD70), aiming to enable avidity-driven T cell-mediated killing of AML cells coexpressing at least two of the antigens. In vitro, MP0533 induced selective T cell-mediated killing of AML cell lines, as well as patient-derived AML blasts and LSCs, expressing two or more target antigens, while sparing healthy HSCs, blood, and endothelial cells. The higher selectivity also resulted in markedly lower levels of cytokine release in normal human blood compared to single antigen-targeting T-cell engagers. In xenograft AML mice models, MP0533 induced tumor-localized T-cell activation and cytokine release, leading to complete eradication of the tumors while having no systemic adverse effects. These studies show that the multispecific-targeting strategy used with MP0533 holds promise for improved selectivity toward LSCs and efficacy against clonal heterogeneity, potentially bringing a new therapeutic option to this group of patients with a high unmet need. MP0533 is currently being evaluated in a dose-escalation phase 1 study in patients with relapsed or refractory AML (NCT05673057).
急性髓系白血病 (AML) 患者的预后有限,尤其是不适合接受造血干细胞 (HSC) 移植的老年或体弱患者。该疾病由白血病干细胞 (LSCs) 驱动,这些细胞的特征是克隆异质性和对常规治疗的耐药性。因此,这些细胞被认为是疾病进展和复发的主要原因。我们设计了 MP0533,这是一种多特异性 CD3 结合设计的锚蛋白重复蛋白 (DARPin),可以同时结合 AML 细胞上的三种抗原(CD33、CD123 和 CD70),旨在使至少表达两种抗原的 AML 细胞能够通过亲和力驱动的 T 细胞介导的杀伤。在体外,MP0533 诱导了表达两种或更多靶抗原的 AML 细胞系、患者来源的 AML blasts 和 LSCs 的选择性 T 细胞介导的杀伤,同时对健康的 HSCs、血液和内皮细胞具有保护作用。更高的选择性也导致与单抗原靶向 T 细胞结合物相比,在正常人血液中细胞因子释放水平明显降低。在异种移植 AML 小鼠模型中,MP0533 诱导肿瘤局部 T 细胞激活和细胞因子释放,导致肿瘤完全消除,而没有全身不良反应。这些研究表明,MP0533 所采用的多特异性靶向策略具有提高对 LSCs 的选择性和对抗克隆异质性的疗效的潜力,为这群具有高度未满足需求的患者带来了新的治疗选择。MP0533 目前正在复发或难治性 AML 患者的剂量递增 1 期研究中进行评估(NCT05673057)。