Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.
Cancer Cell. 2020 Dec 14;38(6):788-802. doi: 10.1016/j.ccell.2020.08.004. Epub 2020 Sep 17.
Pancreatic ductal adenocarcinoma (PDA) is among the most immune-resistant tumor types. Its unique genomic landscape shaped by oncogenic drivers promotes immune suppression from the earliest stages of tumor inception to subvert adaptive T cell immunity. Single-agent immune modulators have thus far proven clinically ineffective, and multi-modal therapies targeting mechanisms of immunotherapy resistance are likely needed. Here, we review novel immunotherapy strategies currently under investigation to (1) confer antigen specificity, (2) enhance T cell effector function, and (3) neutralize immunosuppressive elements within the tumor microenvironment that may be rationally combined to untangle the web of immune resistance in PDA and other tumors.
胰腺导管腺癌(PDA)是最具免疫抵抗性的肿瘤类型之一。其由致癌驱动因素塑造的独特基因组景观促进了从肿瘤发生的最早阶段到颠覆适应性 T 细胞免疫的免疫抑制。因此,单一药物免疫调节剂在临床上已被证明无效,可能需要针对免疫治疗耐药机制的多模式治疗。在这里,我们综述了目前正在研究的新型免疫治疗策略,以(1)赋予抗原特异性,(2)增强 T 细胞效应功能,以及(3)中和肿瘤微环境中的免疫抑制成分,这些策略可能会被合理组合,以解开 PDA 和其他肿瘤中免疫抵抗的复杂网络。