Program in Immunology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109.
Program in Immunology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109
J Immunol. 2018 Jan 15;200(2):459-468. doi: 10.4049/jimmunol.1701155.
Immunotherapy with T cells genetically modified to express chimeric Ag receptors (CARs) that target tumor-associated molecules have impressive efficacy in hematological malignancies. The field has now embraced the challenge of applying this approach to treat common epithelial malignancies, which make up the majority of cancer cases but evade immunologic attack by a variety of subversive mechanisms. In this study, we review the principles that have guided CAR T cell design and the extraordinary clinical results being achieved in B cell malignancies targeting CD19 with a single infusion of engineered T cells. This success has raised expectations that CAR T cells can be applied to solid tumors, but numerous obstacles must be overcome to achieve the success observed in hematologic cancers. Potential solutions driven by advances in genetic engineering, synthetic biology, T cell biology, and improved tumor models that recapitulate the obstacles in human tumors are discussed.
经基因修饰表达嵌合抗原受体(CAR)的 T 细胞免疫疗法靶向肿瘤相关分子,在血液恶性肿瘤中具有显著疗效。目前,该领域已经接受了将这一方法应用于治疗常见上皮性恶性肿瘤的挑战,这些恶性肿瘤构成了大多数癌症病例,但通过多种颠覆机制逃避免疫攻击。在这项研究中,我们回顾了指导 CAR T 细胞设计的原则,以及通过单次输注工程化 T 细胞靶向 CD19 在 B 细胞恶性肿瘤中取得的非凡临床结果。这一成功带来了将 CAR T 细胞应用于实体瘤的期望,但要实现血液癌症中观察到的成功,还必须克服许多障碍。讨论了由基因工程、合成生物学、T 细胞生物学和改进的肿瘤模型的进步驱动的潜在解决方案,这些模型重现了人类肿瘤中的障碍。