Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Department of Dermatology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Oncoimmunology. 2021 Nov 27;10(1):2006893. doi: 10.1080/2162402X.2021.2006893. eCollection 2021.
Immune checkpoint inhibitors (ICIs) have improved the survival of patients with non-small cell lung cancer (NSCLC) by reinvigorating tumor-specific T cell responses. However, the specificity of such T cells and the human leukocyte antigen (HLA)-associated epitopes recognized, remain elusive. In this study, we identified NSCLC T cell epitopes of recently described NSCLC-associated antigens, termed keratinocyte differentiation antigens. Epitopes of these antigens were presented by HLA-A 03:01 and HLA-C 04:01 and were associated with responses to ICI therapy. Patients with CD8 T cell responses to these epitopes had improved overall and progression-free survival. T cells specific for such epitopes could eliminate HLA class I-matched NSCLC cells and were enriched in patient lung tumors. The identification of novel lung cancer HLA-associated epitopes that correlate with improved ICI-dependent treatment outcomes suggests that keratinocyte-specific proteins are important tumor-associated antigens in NSCLC. These findings improve our understanding of the mechanisms of ICI therapy and may help support the development of vaccination strategies to improve ICI-based treatment of these tumors.
免疫检查点抑制剂 (ICIs) 通过重新激活肿瘤特异性 T 细胞反应,提高了非小细胞肺癌 (NSCLC) 患者的生存率。然而,这些 T 细胞的特异性和人类白细胞抗原 (HLA) 相关表位的识别仍然难以捉摸。在这项研究中,我们鉴定了最近描述的与 NSCLC 相关的抗原,即角蛋白分化抗原的 NSCLC T 细胞表位。这些抗原的表位由 HLA-A 03:01 和 HLA-C 04:01 呈递,与 ICI 治疗的反应相关。对这些表位有 CD8 T 细胞反应的患者具有更好的总生存期和无进展生存期。针对这些表位的 T 细胞可以消除 HLA Ⅰ类匹配的 NSCLC 细胞,并且在患者的肺肿瘤中富集。鉴定与改善 ICI 依赖性治疗结果相关的新型肺癌 HLA 相关表位表明,角蛋白特异性蛋白是非小细胞肺癌中的重要肿瘤相关抗原。这些发现提高了我们对 ICI 治疗机制的理解,并可能有助于支持疫苗接种策略的发展,以改善基于 ICI 的这些肿瘤的治疗。