Jackson Stephanie R, Yuan Jinyun, Teague Ryan M
Saint Louis University School of Medicine, Department of Molecular Microbiology & Immunology, 1100 South Grand Blvd, St Louis, MO 63104, USA.
Immunotherapy. 2014;6(7):833-52. doi: 10.2217/imt.14.51.
In the final issue of Science in 2013, the American Association of Science recognized progress in the field of cancer immunotherapy as the 'Breakthrough of the Year.' The achievements were actually twofold, owing to the early success of genetically engineered chimeric antigen receptors (CAR) and to the mounting clinical triumphs achieved with checkpoint blockade antibodies. While fundamentally very different, the common thread of these independent strategies is the ability to prevent or overcome mechanisms of CD8(+) T-cell tolerance for improved tumor immunity. Here we discuss how circumventing T-cell tolerance has provided experimental insights that have guided the field of clinical cancer immunotherapy to a place where real breakthroughs can finally be claimed.
在2013年《科学》杂志的最后一期中,美国科学促进会将癌症免疫治疗领域的进展认定为“年度突破”。这一成就实际上有两方面,一方面是基因工程嵌合抗原受体(CAR)取得的早期成功,另一方面是检查点阻断抗体在临床上取得的越来越多的胜利。虽然这两种独立策略在根本上有很大不同,但它们的共同主线是能够预防或克服CD8(+) T细胞耐受机制,以提高肿瘤免疫。在此,我们讨论规避T细胞耐受如何提供了实验性见解,这些见解将临床癌症免疫治疗领域引领至一个最终能够实现真正突破的阶段。