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腺病毒治疗传递细胞因子和检查点抑制剂增强 CAR T 细胞对转移性头颈部癌症的作用。

Adenovirotherapy Delivering Cytokine and Checkpoint Inhibitor Augments CAR T Cells against Metastatic Head and Neck Cancer.

机构信息

Department of Medicine, Baylor College of Medicine, Houston, TX, USA; Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, TX, USA.

Department of Otolaryngology, Baylor College of Medicine, Houston, TX, USA.

出版信息

Mol Ther. 2017 Nov 1;25(11):2440-2451. doi: 10.1016/j.ymthe.2017.09.010. Epub 2017 Sep 14.

Abstract

In solid tumors, chimeric antigen receptor (CAR)-modified T cells must overcome the challenges of the immunosuppressive tumor microenvironment. We hypothesized that pre-treating tumors with our binary oncolytic adenovirus (CAd), which produces local oncolysis and expresses immunostimulatory molecules, would enhance the antitumor activity of HER2-specific CAR T cells, which alone are insufficient to cure solid tumors. We tested multiple cytokines in conjunction with PD-L1-blocking antibody and found that Ad-derived IL-12p70 prevents the loss of HER2.CAR-expressing T cells at the tumor site. Accordingly, we created a construct encoding the PD-L1-blocking antibody and IL-12p70 (CAd12_PDL1). In head and neck squamous cell carcinoma (HNSCC) xenograft models, combining local treatment with CAd12_PDL1 and systemic HER2.CAR T cell infusion improved survival to >100 days compared with approximately 25 days with either approach alone. This combination also controlled both primary and metastasized tumors in an orthotopic model of HNSCC. Overall, our data show that CAd12_PDL1 augments the anti-tumor effects of HER2.CAR T cells, thus controlling the growth of both primary and metastasized tumors.

摘要

在实体瘤中,嵌合抗原受体(CAR)修饰的 T 细胞必须克服免疫抑制肿瘤微环境的挑战。我们假设,用我们的二元溶瘤腺病毒(CAd)预处理肿瘤,该病毒可产生局部溶瘤并表达免疫刺激分子,将增强 HER2 特异性 CAR T 细胞的抗肿瘤活性,而单独使用 CAR T 细胞不足以治愈实体瘤。我们测试了多种细胞因子与 PD-L1 阻断抗体的联合作用,发现腺病毒衍生的 IL-12p70 可防止肿瘤部位表达 HER2.CAR 的 T 细胞丢失。因此,我们构建了一个编码 PD-L1 阻断抗体和 IL-12p70 的构建体(CAd12_PDL1)。在头颈部鳞状细胞癌(HNSCC)异种移植模型中,与单独使用 CAd12_PDL1 局部治疗和全身输注 HER2.CAR T 细胞相比,联合治疗可将存活时间延长至>100 天,而单独使用任一方法的存活时间约为 25 天。这种联合治疗还控制了 HNSCC 原位模型中的原发性和转移性肿瘤。总体而言,我们的数据表明,CAd12_PDL1 增强了 HER2.CAR T 细胞的抗肿瘤作用,从而控制了原发性和转移性肿瘤的生长。

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