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CD161⁺CD8⁺ T 细胞匮乏的人胰腺癌临床结局不良及免疫逃逸微环境

英文原题:Poor clinical outcomes and immunoevasive contexture in CD161(+)CD8(+) T cells barren human pancreatic cancer.

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Poor clinical outcomes and immunoevasive contexture in CD161(+)CD8(+) T cells barren human pancreatic cancer.

PubMed 2024/03/26(内容时间) J Immunother Cancer Q1 · IF 11.7(JCR 2025)

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研究概要

CD161 + CD8 + T 细胞表现出细胞毒性和免疫检查点分子水平升高,提示其作为免疫治疗潜在且有吸引力的靶点。肿瘤浸润性 CD161 + CD8 + T 细胞是 PDAC 生存及辅助化疗治疗反应的有价值且有望的预测指标。需要进一步研究以验证其在风险分层和治疗策略优化中的作用。

研究思路结论见上方概要

CD161在CD8+ T细胞上的表达在肿瘤免疫学中的作用已在少数研究中进行了探索,而CD161+CD8+T细胞在胰腺导管腺癌(PDAC)中的临床意义仍不清楚。本研究旨在阐明PDAC中CD161+CD8+T细胞浸润相关的预后价值和分子特征。

本研究纳入186例根治性切除术后经组织学确诊为PDAC的患者。采用肿瘤组织芯片免疫荧光染色评估CD161 + CD8 + T细胞浸润情况。采用流式细胞术和单细胞RNA测序评估其功能状态。

我们观察到肿瘤浸润性CD161 + CD8 + T细胞与临床病理因素(如肿瘤分化、神经周围侵犯和血清CA19-9水平)之间存在显著关联。肿瘤浸润性CD161 + CD8 + T细胞水平较高的患者比水平较低的患者具有更长的总生存期(OS)和无复发生存期(RFS)。多变量分析证实,肿瘤浸润性CD161 + CD8 + T细胞是OS和RFS的独立预后指标。值得注意的是,肿瘤浸润性CD161 + CD8 + T细胞与CA19-9水平的联合在生存预测方面显示出更优的效能,且肿瘤浸润性CD161 + CD8 + T细胞低而CA19-9水平高的患者生存最差。此外,较低的肿瘤浸润性CD161 + CD8 + T细胞与对辅助化疗更好的反应相关。最后,我们将肿瘤浸润性CD161 + CD8 + T细胞鉴定为一种独特的反应性CD8 + T细胞亚型,其特征是细胞毒性细胞因子和免疫检查点分子水平升高。

展开英文摘要原文

The role of CD161 expression on CD8 + T cells in tumor immunology has been explored in a few studies, and the clinical significance of CD161 + CD8 + T cells in pancreatic ductal adenocarcinoma (PDAC) remains unclear. This study seeks to clarify the prognostic value and molecular characteristics linked to CD161 + CD8 + T cell infiltration in PDAC.

This study included 186 patients with confirmed PDAC histology after radical resection. CD161 + CD8 + T cell infiltration was assessed using immunofluorescence staining on tumor microarrays. Flow cytometry and single-cell RNA sequencing were used to evaluate their functional status.

We observed significant associations between tumor-infiltrating CD161 + CD8 + T cells and clinicopathological factors, such as tumor differentiation, perineural invasion, and serum CA19-9 levels. Patients with higher tumor-infiltrating CD161 + CD8 + T cell levels had longer overall survival (OS) and recurrence-free survival (RFS) than those with lower levels. Multivariable analysis confirmed tumor-infiltrating CD161 + CD8 + T cell as an independent prognostic indicator for both OS and RFS. Notably, a combination of tumor-infiltrating CD161 + CD8 + T cell and CA19-9 levels showed a superior power for survival prediction, and patients with low tumor-infiltrating CD161 + CD8 + T cell and high CA19-9 levels had the worst survival. Furthermore, lower tumor-infiltrating CD161 + CD8 + T cells were associated with a better response to adjuvant chemotherapy. Finally, we identified tumor-infiltrating CD161 + CD8 + T cells as a unique subtype of responsive CD8 + T cells characterized by increased levels of cytotoxic cytokines and immune checkpoint molecules.

CD161 + CD8 + T cells exhibit elevated levels of both cytotoxic and immune-checkpoint molecules, indicating as a potential and attractive target for immunotherapy. The tumor-infiltrating CD161 + CD8 + T cell is a valuable and promising predictor for survival and therapeutic response to adjuvant chemotherapy in PDAC. Further research is warranted to validate its role in the risk stratification and optimization of therapeutic strategies.

论文信息

作者
Chen Q、Yin H、Jiang Z、He T、Xie Y、Mao W、Han J、Liu S
第一作者单位
Department of Pancreatic Surgery, Zhongshan Hospital Fudan University, Shanghai, China.China
通讯作者单位
Department of Pancreatic Surgery, Zhongshan Hospital Fudan University, Shanghai, China npu15@fudan.edu.cn liu.liang@zs-hospital.sh.cn.China
文献类型
非美国政府资助研究
期刊
Journal for immunotherapy of cancer2024 Mar 26
原文标识
PubMed 38531664 · DOI 10.1136/jitc-2023-008694