在切除的人类食管腺癌中,PD-1 和 CD39 阳性 CD8+ 组织常驻 T 淋巴细胞的高比例与更好的临床预后相关。

IF 4.6 2区 医学 Q2 IMMUNOLOGY Cancer Immunology, Immunotherapy Pub Date : 2024-09-05 DOI:10.1007/s00262-024-03799-y
Samuel L Hill, Gessa Sugiyarto, Jack Harrington, Edward James, Timothy J Underwood, Tim Elliott
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引用次数: 0

摘要

目的了解食管腺癌(OAC)CD8+肿瘤浸润淋巴细胞(TIL)区系的淋巴细胞衰竭标志物和组织驻留情况,并确定不同治疗反应背后的可能原因:设计:通过流式细胞术评估了44例接受根治性切除术的食管腺癌患者的肿瘤样本中抗原经验丰富的TIL以及活化和衰竭标记物的存在情况。对 PD-1 和 CD39 阳性的 OAC TILs 群体进行分拣,并使用改良的 SmartSeq2 方案进行批量 RNA 测序。完成了流式细胞术功能评估:结果:抗原经验丰富的 CD8+ OAC TILs 比例越高,术后生存率越高;同时,这些 TILs 的 PD-1 和 CD39 双阳性 (DP) 也与预后有显著相关性。这些双阳性 TIL 中的少数群体对衰竭标记物 TIM3 和 LAG3 呈阳性。对 PD-1 和 CD39 DP TIL 的转录组学评估显示,组织常驻记忆 T 淋巴细胞(TRM)表型的富集与其他癌症生存率的提高有关,流式细胞术显示的典型 TRM 标记 CD103 阳性则进一步证实了这一点。这一群体在其转录组图谱和流式细胞术评估中都显示出了维持功能的能力,并保留了增殖能力:结论:切除的 OAC 会受到 PD-1 和 CD39 DP TIL 的不同程度浸润,淋巴细胞中这种 DP TIL 的丰富程度与生存率的提高有关。与 DN 相比,这种 DP 群体的 TIM3 和 LAG3 阳性率更高,但仍不高,而且符合有功能能力的 TRM 表型。
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High proportion of PD-1 and CD39 positive CD8+ tissue resident T lymphocytes correlates with better clinical outcome in resected human oesophageal adenocarcinoma.

Objective: To understand the CD8+ tumour infiltrating lymphocyte (TIL) compartment of oesophageal adenocarcinoma (OAC) with regards to markers of lymphocyte exhaustion, tissue residency and to identify possible reasons behind differential responses to therapy.

Design: Tumour samples from 44 patients undergoing curative resection for OAC were assessed by flow cytometry for presence of antigen-experienced TILs and markers of activation and exhaustion. Populations of PD-1 and CD39 positive OAC TILs were sorted, and bulk RNA sequencing undertaken using a modified SmartSeq2 protocol. Flow cytometric assessment of functionality was completed.

Results: A higher proportion of antigen experienced CD8+ OAC TILs was associated with improved survival following surgery; while, high double positivity (DP) for PD-1 and CD39 among these TILs also correlated significantly with outcome. These DP TILs possess a minority population which is positive for the markers of exhaustion TIM3 and LAG3. Transcriptomic assessment of the PD-1 and CD39 DP TILs demonstrated enrichment for a tissue resident memory T lymphocyte (TRM) phenotype associated with improved survival in other cancers, reinforced by positivity for the canonical TRM marker CD103 by flow cytometry. This population demonstrated maintained functional capacity both in their transcriptomic profile, and on flow cytometric assessment, as well as preserved proliferative capacity.

Conclusion: Resected OAC are variably infiltrated by PD-1 and CD39 DP TILs, an abundance of which among lymphocytes is associated with improved survival. This DP population has an increased, but still modest, frequency of TIM3 and LAG3 positivity compared to DN, and is in keeping with a functionally competent TRM phenotype.

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来源期刊
CiteScore
10.50
自引率
1.70%
发文量
207
审稿时长
1 months
期刊介绍: Cancer Immunology, Immunotherapy has the basic aim of keeping readers informed of the latest research results in the fields of oncology and immunology. As knowledge expands, the scope of the journal has broadened to include more of the progress being made in the areas of biology concerned with biological response modifiers. This helps keep readers up to date on the latest advances in our understanding of tumor-host interactions. The journal publishes short editorials including "position papers," general reviews, original articles, and short communications, providing a forum for the most current experimental and clinical advances in tumor immunology.
期刊最新文献
HLA-G high-expressor 3'UTR markers are linked to gastric cancer development and survival. Hepatitis associated with immune checkpoint inhibitors-based combinations of other therapies: A real-world pharmacovigilance analysis based on the FDA adverse event reporting system (FAERS) database. Hepatic arterial infusion chemotherapy combined with systemic therapy sequentially or simultaneously for advanced hepatocellular carcinoma. "Tumor immunology meets oncology" (TIMO), 18 April-20 April 2024, in Brandenburg an der Havel, Germany. Cryo-thermal therapy reshaped the tumor immune microenvironment to enhance the efficacy of adoptive T cell therapy.
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