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用于癌症免疫治疗的免疫调节抗体药物偶联物(IM-ADC)。

Immune Modulating Antibody-Drug Conjugate (IM-ADC) for Cancer Immunotherapy.

作者信息

He Lei, Wang Liangliang, Wang Zhisong, Li Tiantian, Chen Hui, Zhang Yaning, Hu Zeping, Dimitrov Dimiter S, Du Juanjuan, Liao Xuebin

机构信息

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.

出版信息

J Med Chem. 2021 Nov 11;64(21):15716-15726. doi: 10.1021/acs.jmedchem.1c00961. Epub 2021 Nov 3.

Abstract

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.

摘要

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。

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