Dovedi Simon J, Elder Matthew J, Yang Chunning, Sitnikova Suzanne I, Irving Lorraine, Hansen Anna, Hair James, Jones Des C, Hasani Sumati, Wang Bo, Im Seock-Ah, Tran Ben, Subramaniam Deepa S, Gainer Shelby D, Vashisht Kapil, Lewis Arthur, Jin Xiaofang, Kentner Stacy, Mulgrew Kathy, Wang Yaya, Overstreet Michael G, Dodgson James, Wu Yanli, Palazon Asis, Morrow Michelle, Rainey Godfrey J, Browne Gareth J, Neal Frances, Murray Thomas V, Toloczko Aleksandra D, Dall'Acqua William, Achour Ikbel, Freeman Daniel J, Wilkinson Robert W, Mazor Yariv
Early Oncology R&D, AstraZeneca, Cambridge, United Kingdom.
Antibody Discovery and Protein Engineering, R&D, AstraZeneca, Gaithersburg, Maryland.
Cancer Discov. 2021 May;11(5):1100-1117. doi: 10.1158/2159-8290.CD-20-1445. Epub 2021 Jan 8.
The clinical benefit of PD-1 blockade can be improved by combination with CTLA4 inhibition but is commensurate with significant immune-related adverse events suboptimally limiting the doses of anti-CTLA4 mAb that can be used. MEDI5752 is a monovalent bispecific antibody designed to suppress the PD-1 pathway and provide modulated CTLA4 inhibition favoring enhanced blockade on PD-1 activated T cells. We show that MEDI5752 preferentially saturates CTLA4 on PD-1 T cells versus PD-1 T cells, reducing the dose required to elicit IL2 secretion. Unlike conventional PD-1/CTLA4 mAbs, MEDI5752 leads to the rapid internalization and degradation of PD-1. Moreover, we show that MEDI5752 preferentially localizes and accumulates in tumors providing enhanced activity when compared with a combination of mAbs targeting PD-1 and CTLA4 . Following treatment with MEDI5752, robust partial responses were observed in two patients with advanced solid tumors. MEDI5752 represents a novel immunotherapy engineered to preferentially inhibit CTLA4 on PD-1 T cells. SIGNIFICANCE: The unique characteristics of MEDI5752 represent a novel immunotherapy engineered to direct CTLA4 inhibition to PD-1 T cells with the potential for differentiated activity when compared with current conventional mAb combination strategies targeting PD-1 and CTLA4. This molecule therefore represents a step forward in the rational design of cancer immunotherapy...
将PD-1阻断与CTLA4抑制联合使用可提高临床获益,但这与显著的免疫相关不良事件相关,从而不理想地限制了可使用的抗CTLA4单克隆抗体的剂量。MEDI5752是一种单价双特异性抗体,旨在抑制PD-1通路,并提供调节性CTLA4抑制,有利于增强对PD-1激活的T细胞的阻断。我们发现,与PD-1阴性T细胞相比,MEDI5752优先使PD-1阳性T细胞上的CTLA4饱和,从而降低引发IL2分泌所需的剂量。与传统的PD-1/CTLA4单克隆抗体不同,MEDI5752导致PD-1快速内化和降解。此外,我们发现,与靶向PD-1和CTLA4的单克隆抗体联合使用相比,MEDI5752优先在肿瘤中定位和积累,从而提供增强的活性。用MEDI5752治疗后,两名晚期实体瘤患者出现了显著的部分缓解。MEDI5752代表了一种新型免疫疗法,其设计目的是优先抑制PD-1阳性T细胞上的CTLA4。意义:MEDI5752的独特特性代表了一种新型免疫疗法,其设计目的是将CTLA4抑制作用导向PD-1阳性T细胞,与目前针对PD-1和CTLA4的传统单克隆抗体联合策略相比,具有产生差异化活性的潜力。因此,这种分子代表了癌症免疫疗法合理设计方面的一个进步……