He Lei, Wang Liangliang, Wang Zhisong, Li Tiantian, Chen Hui, Zhang Yaning, Hu Zeping, Dimitrov Dimiter S, Du Juanjuan, Liao Xuebin
School of Pharmaceutical Sciences, Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100084, China.
Advanced Innovation Center for Human Brain Protection, Beijing Tiantan Hospital, Capital Medical University, Beijing 100088, China.
J Med Chem. 2021 Nov 11;64(21):15716-15726. doi: 10.1021/acs.jmedchem.1c00961. Epub 2021 Nov 3.
Antibody-drug conjugate (ADC) and immune checkpoint blockade (ICB) offer promising approaches for cancer treatment. Here, we describe an ADC constructed by conjugating anti-PD-L1 THIOMAB with a bifunctional immunomodulator via a redox-cleavable linker. The resulting ADC not only triggers a potent antitumor immune response by blocking the PD-1/PD-L1 interaction and activating the Toll-like receptor 7/8 (TLR7/8) signaling pathway but also upregulates its targeted PD-L1 expression via epigenetic regulation and/or IFN-γ induction, thus conferring more sensitivity to the PD-1/PD-L1 blockade. We identify that ADC treatment could lead to more pronounced tumor suppression than the treatment of in combination with the anti-PD-L1 antibody. Accordingly, this study provides a novel ADC strategy to enhance the antitumor immune response to ICB therapy.
抗体药物偶联物(ADC)和免疫检查点阻断(ICB)为癌症治疗提供了有前景的方法。在此,我们描述了一种通过氧化还原可裂解连接子将抗PD-L1硫醇单克隆抗体与双功能免疫调节剂偶联构建的ADC。所得的ADC不仅通过阻断PD-1/PD-L1相互作用和激活Toll样受体7/8(TLR7/8)信号通路触发强大的抗肿瘤免疫反应,还通过表观遗传调控和/或IFN-γ诱导上调其靶向的PD-L1表达,从而赋予对PD-1/PD-L1阻断更高的敏感性。我们发现,与抗PD-L1抗体联合治疗相比,ADC治疗可导致更显著的肿瘤抑制。因此,本研究提供了一种新的ADC策略,以增强对ICB治疗的抗肿瘤免疫反应。