Tran Eric, Robbins Paul F, Lu Yong-Chen, Prickett Todd D, Gartner Jared J, Jia Li, Pasetto Anna, Zheng Zhili, Ray Satyajit, Groh Eric M, Kriley Isaac R, Rosenberg Steven A
From the Surgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD.
N Engl J Med. 2016 Dec 8;375(23):2255-2262. doi: 10.1056/NEJMoa1609279.
We identified a polyclonal CD8+ T-cell response against mutant KRAS G12D in tumor-infiltrating lymphocytes obtained from a patient with metastatic colorectal cancer. We observed objective regression of all seven lung metastases after the infusion of approximately 1.11×10 HLA-C08:02-restricted tumor-infiltrating lymphocytes that were composed of four different T-cell clonotypes that specifically targeted KRAS G12D. However, one of these lesions had progressed on evaluation 9 months after therapy. The lesion was resected and found to have lost the chromosome 6 haplotype encoding the HLA-C08:02 class I major histocompatibility complex (MHC) molecule. The loss of expression of this molecule provided a direct mechanism of tumor immune evasion. Thus, the infusion of CD8+ cells targeting mutant KRAS mediated effective antitumor immunotherapy against a cancer that expressed mutant KRAS G12D and HLA-C*08:02.
我们在一名转移性结直肠癌患者的肿瘤浸润淋巴细胞中鉴定出针对突变型KRAS G12D的多克隆CD8 + T细胞反应。在输注约1.11×10个由四种不同T细胞克隆型组成的HLA-C08:02限制性肿瘤浸润淋巴细胞后,我们观察到所有七个肺转移灶均出现客观消退,这些T细胞克隆型特异性靶向KRAS G12D。然而,其中一个病灶在治疗后9个月的评估中出现进展。该病灶被切除,发现其丢失了编码HLA-C08:02 I类主要组织相容性复合体(MHC)分子的6号染色体单倍型。该分子表达的缺失提供了肿瘤免疫逃逸的直接机制。因此,输注靶向突变型KRAS的CD8 +细胞介导了针对表达突变型KRAS G12D和HLA-C*08:02的癌症的有效抗肿瘤免疫治疗。