Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Center for Cell and Gene Therapy, Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA.
Mol Ther. 2022 Sep 7;30(9):2881-2890. doi: 10.1016/j.ymthe.2022.07.006. Epub 2022 Jul 12.
Chimeric antigen receptor (CAR) T cell therapy has created a paradigm shift in the treatment of hematologic malignancies but has not been as effective toward solid tumors. For such tumors, the primary obstacles facing CAR T cells are scarcity of tumor-specific antigens and the hostile and complex tumor microenvironment. Glycosylation, the process by which sugars are post-translationally added to proteins or lipids, is profoundly dysregulated in cancer. Abnormally glycosylated glycoproteins expressed on cancer cells offer unique targets for CAR T therapy as they are specific to tumor cells. Tumor stromal cells also express abnormal glycoproteins and thus also have the potential to be targeted by glycan-binding CAR T cells. This review will discuss the state of CAR T cells in the therapy of solid tumors, the cancer glycoproteome and its potential for use as a therapeutic target, and the landscape and future of glycan-binding CAR T cell therapy.
嵌合抗原受体 (CAR) T 细胞疗法在血液系统恶性肿瘤的治疗中带来了范式转变,但对实体瘤的疗效并不理想。对于此类肿瘤,CAR T 细胞面临的主要障碍是肿瘤特异性抗原的缺乏和恶劣且复杂的肿瘤微环境。糖基化是指糖在蛋白质或脂质上的翻译后添加过程,在癌症中受到严重的失调。癌细胞表面表达的异常糖基化糖蛋白是 CAR T 治疗的独特靶点,因为它们是肿瘤细胞特有的。肿瘤基质细胞也表达异常糖蛋白,因此也有可能成为糖结合 CAR T 细胞的靶点。这篇综述将讨论 CAR T 细胞在实体瘤治疗中的现状、癌症糖组及其作为治疗靶点的潜力,以及糖结合 CAR T 细胞治疗的现状和未来。