Pardoll Drew
Department of Oncology and Director Cancer Immunology Program, Johns Hopkins University School of Medicine and Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD.
Semin Oncol. 2015 Aug;42(4):523-38. doi: 10.1053/j.seminoncol.2015.05.003. Epub 2015 Jun 3.
A number of consensuses regarding cancer immunology have recently emerged from both preclinical immunotherapy models and analysis of cancer patients. First and foremost, the natural state of endogenous tumor reactive T cells is characterized by general hyporesponsiveness or anergy. This is likely due to a number of mechanisms that tumors use to induce tolerance as they develop. While many of the newer generation vaccines can effectively transfer antigen to and activate dendritic cells, T-cell tolerance remains a major barrier that is difficult to overcome by vaccination alone. Preclinical models demonstrate that for poorly immunogenic tumors, once tolerance has been established, therapeutic vaccines alone are ineffective at curing animals with a significant established tumor burden. However, combination strategies of vaccination together with inhibitors of immunologic checkpoints and agonists for co-stimulatory pathways are proving capable of overcoming tolerance and generating significant anti-tumor responses even in cases of established metastatic cancer.
最近,从临床前免疫治疗模型和癌症患者分析中得出了一些关于癌症免疫学的共识。首先,内源性肿瘤反应性T细胞的自然状态的特征是普遍反应低下或无反应。这可能是由于肿瘤在发展过程中用于诱导耐受的多种机制。虽然许多新一代疫苗可以有效地将抗原传递给树突状细胞并激活它们,但T细胞耐受仍然是一个主要障碍,仅靠疫苗接种很难克服。临床前模型表明,对于免疫原性较差的肿瘤,一旦建立了耐受,单独使用治疗性疫苗对于治愈具有显著肿瘤负荷的动物是无效的。然而,疫苗接种与免疫检查点抑制剂和共刺激途径激动剂的联合策略已被证明能够克服耐受,甚至在已发生转移的癌症病例中也能产生显著的抗肿瘤反应。