Medizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, Würzburg, Germany.
Curr Opin Oncol. 2020 Sep;32(5):510-517. doi: 10.1097/CCO.0000000000000653.
Immunotherapy with gene-engineered chimeric antigen receptor (CAR)-T cells has curative potential in advanced malignancies and undergoes a surging preclinical and clinical development. Here, we present a selection of new targets and technologies that illustrate the progress that is being made with the aspiration to make CAR-T cell therapy a universally applicable and effective treatment in cancer medicine.
There is a rich pipeline of new target antigens for CAR-T cells in hematology and oncology that are rated based on uniformity but also stability of expression on tumor cells under therapeutic pressure. New technologies in CAR-T cell engineering are directed at neutralizing inhibitory ligands and factors in the tumor microenvironment, preventing CAR-T cell exhaustion and enhancing selectivity for tumor cells with 'smart' CAR designs. The manufacture of CAR-T cells using virus-free protocols is anticipated to reduce supply-chain complexity and to improve patient access.
CD19 CAR-T cell therapy is an approved treatment for B-cell leukemia and -lymphoma and considering the current 'target and technology' pipeline, we anticipate that additional CAR-T cell products will accomplish their 'breakthrough' and clinical proof-of-concept in other indications in hematology and in oncology. Technologies to enhance therapeutic index and facilitate manufacturing will be key for assuring availability and accessibility of CAR-T cell products and their implementation into routine clinical practice.
基因工程嵌合抗原受体(CAR)-T 细胞免疫疗法在晚期恶性肿瘤中有治愈的潜力,并正在进行大量的临床前和临床开发。在这里,我们选择了一些新的靶点和技术,这些新的靶点和技术展示了在使 CAR-T 细胞疗法成为癌症治疗中普遍适用和有效的治疗方法方面所取得的进展。
在血液学和肿瘤学中有丰富的 CAR-T 细胞新靶点,这些靶点基于肿瘤细胞在治疗压力下表达的均匀性和稳定性进行评估。CAR-T 细胞工程的新技术针对的是中和肿瘤微环境中的抑制性配体和因子,防止 CAR-T 细胞衰竭,并通过“智能”CAR 设计增强对肿瘤细胞的选择性。使用无病毒方案制造 CAR-T 细胞有望降低供应链的复杂性,并提高患者的可及性。
CD19 CAR-T 细胞疗法已被批准用于治疗 B 细胞白血病和淋巴瘤,考虑到目前的“靶点和技术”管道,我们预计其他 CAR-T 细胞产品将在血液学和肿瘤学的其他适应症中实现其“突破”和临床概念验证。增强治疗指数和促进制造的技术将是确保 CAR-T 细胞产品的可用性和可及性并将其纳入常规临床实践的关键。