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HER2 靶向抗体药物偶联物诱导宿主对肿瘤干细胞的免疫反应。

HER2-targeted antibody-drug conjugate induces host immunity against cancer stem cells.

机构信息

University of Michigan Rogel Cancer Center, Ann Arbor, MI 48109, USA; Department of Hematology & Oncology, The Third Affiliated Hospital of Anhui Medical University, Hefei 230032, China.

University of Michigan Rogel Cancer Center, Ann Arbor, MI 48109, USA; Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.

出版信息

Cell Chem Biol. 2021 May 20;28(5):610-624.e5. doi: 10.1016/j.chembiol.2021.02.013. Epub 2021 Mar 11.

Abstract

We previously tested HER2-targeted antibody-drug conjugates (ADCs) in immunocompromised (SCID) mice, precluding evaluation of host immunity, impact on cancer stem cells (CSCs), and potential benefit when combined with PD-L1 blockade. In this study, we tested HER2-targeted ADC in two immunocompetent mouse tumor models. HER2-targeted ADC specifically inhibited the growth of HER2-expressing tumors, prolonged animal survival, and reduced HER2 and PD-L1 cells. ADC + anti-PD-L1 antibody augmented therapeutic efficacy, modulated immune gene signatures, increased the number and function of CD3 and CD19 tumor-infiltrating lymphocytes (TILs), induced tumor antigen-specific immunological memory, stimulated B cell activation, differentiation, and IgG1 production both systemically and in the tumor microenvironment. In addition, ADC therapy modulated T cell subsets and their activation in TILs. Furthermore, HER2-targeted ADC reduced the number and tumorigenicity of ALDH CSCs. This study demonstrates that HER2-targeted ADC effectively targets ALDH CSCs and this effect is augmented by co-administration of anti-PD-L1 antibody.

摘要

我们之前在免疫缺陷 (SCID) 小鼠中测试了针对 HER2 的抗体药物偶联物 (ADC),但无法评估宿主免疫、对癌症干细胞 (CSC) 的影响,以及与 PD-L1 阻断联合使用的潜在益处。在这项研究中,我们在两种免疫功能正常的小鼠肿瘤模型中测试了针对 HER2 的 ADC。HER2 靶向 ADC 特异性抑制 HER2 表达肿瘤的生长,延长动物存活时间,并减少 HER2 和 PD-L1 细胞。ADC+抗 PD-L1 抗体增强了治疗效果,调节了免疫基因特征,增加了 CD3 和 CD19 肿瘤浸润淋巴细胞 (TIL) 的数量和功能,诱导了肿瘤抗原特异性免疫记忆,刺激了 B 细胞的激活、分化和 IgG1 的产生,无论是在全身还是在肿瘤微环境中。此外,ADC 治疗还调节了 TIL 中 T 细胞亚群及其激活。此外,HER2 靶向 ADC 减少了 ALDH CSCs 的数量和致瘤性。这项研究表明,HER2 靶向 ADC 能有效靶向 ALDH CSCs,并且这种效果通过联合使用抗 PD-L1 抗体得到增强。

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