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血管破坏剂 CA4P 提高了 CAR-T 细胞在实体人肿瘤临床前模型中的抗肿瘤疗效。

The Vascular Disrupting Agent CA4P Improves the Antitumor Efficacy of CAR-T Cells in Preclinical Models of Solid Human Tumors.

机构信息

Department of Cell Biology and Stem Cell Research Center, School of Basic Medical Sciences, State Key Laboratory of Natural and Biomimetic Drugs, Peking University Health Science Center, Peking University, Beijing 100191, China.

Department of Cell Biology and Stem Cell Research Center, School of Basic Medical Sciences, State Key Laboratory of Natural and Biomimetic Drugs, Peking University Health Science Center, Peking University, Beijing 100191, China.

出版信息

Mol Ther. 2020 Jan 8;28(1):75-88. doi: 10.1016/j.ymthe.2019.10.010. Epub 2019 Oct 18.

Abstract

Chimeric antigen receptor (CAR) T cell therapy remains relatively ineffective against solid tumors due to inadequate infiltration and in vivo expansion of CAR-T cells. Unlike hematological malignancies, solid tumors have vascular barriers that hinder CAR-T cells from reaching the tumor site. Here, we demonstrated that combretastatin A-4 phosphate (CA4P), a vascular disrupting agent (VDA), can significantly improve the infiltration ability of CAR-T cells in solid tumors as evidenced by elevated levels of IFN-γ. Moreover, combined treatment with CA4P and CAR-T cells greatly increased the therapeutic efficiency of the CAR-T cells in subcutaneous ovarian cancer mouse xenograft models and patient-derived xenograft (PDX) models of colon and ovarian carcinoma. Our findings highlight CA4P as an effective antitumor agent candidate for combination with CAR-T cells in clinical applications to treat solid tumors.

摘要

嵌合抗原受体 (CAR) T 细胞疗法对实体瘤的疗效相对较差,这是由于 CAR-T 细胞在体内的浸润和扩增不足所致。与血液恶性肿瘤不同,实体瘤具有血管屏障,阻碍 CAR-T 细胞到达肿瘤部位。在这里,我们证明了 combretastatin A-4 磷酸盐 (CA4P),一种血管破坏剂 (VDA),可以显著提高 CAR-T 细胞在实体瘤中的浸润能力,这一点可以从 IFN-γ水平的升高得到证明。此外,CA4P 与 CAR-T 细胞联合治疗大大提高了 CAR-T 细胞在皮下卵巢癌小鼠异种移植模型和结肠癌和卵巢癌患者来源异种移植 (PDX) 模型中的治疗效率。我们的研究结果强调了 CA4P 作为一种有效的抗肿瘤候选药物,可与 CAR-T 细胞联合应用于临床治疗实体瘤。

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