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免疫检查点抑制剂治疗 NSCLC 患者的角蛋白细胞分化抗原特异性 T 细胞与改善生存相关。

Keratinocyte differentiation antigen-specific T cells in immune checkpoint inhibitor-treated NSCLC patients are associated with improved survival.

机构信息

Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Department of Dermatology, Kantonsspital St. Gallen, St. Gallen, Switzerland.

出版信息

Oncoimmunology. 2021 Nov 27;10(1):2006893. doi: 10.1080/2162402X.2021.2006893. eCollection 2021.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87c7/8632109/335360270053/KONI_A_2006893_F0001_B.jpg

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