Lymphocyte activation gene-3 (LAG3) mRNA and protein expression on tumour infiltrating lymphocytes (TILs) in oesophageal adenocarcinoma

被引:29
作者
Gebauer, Florian [1 ]
Kraemer, Max [2 ]
Bruns, Christiane [1 ]
Schloesser, Hans A. [1 ]
Thelen, Martin [1 ]
Lohneis, Philipp [2 ]
Schroeder, Wolfgang [1 ,4 ]
Zander, Thomas [3 ,4 ]
Alakus, Hakan [1 ]
Buettner, Reinhard [2 ]
Loeser, Heike [2 ]
Quaas, Alexander [2 ]
机构
[1] Univ Cologne, Dept Gen Visceral Tumour & Transplantat Surg, Kerpener Str 62, D-50937 Cologne, Germany
[2] Univ Cologne, Inst Pathol, Cologne, Germany
[3] Univ Cologne, Dept Internal Med 1, Gastrointestinal Canc Grp Cologne GCGC, Ctr Integrated Oncol Aachen Bonn Cologne Duesseld, Cologne, Germany
[4] Univ Cologne, Ctr Mol Med Cologne, Cologne, Germany
关键词
LAG3; Immunohistochemistry; mRNA in-situ; Oesophageal adenocarcinoma; CD8(+) T-CELL; IMMUNE CHECKPOINT; STANDARDIZED METHOD; THERAPEUTIC TARGET; SOLID TUMORS; IMMUNOTHERAPY; PATHOLOGISTS; CARCINOMA; MELANOMA; PROPOSAL;
D O I
10.1007/s00432-020-03295-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Lymphocyte activation gene-3 (LAG3) is an immunosuppressive checkpoint molecule expressed on T cells. The frequency and distribution of LAG3 expression in oesophageal adenocarcinoma (EAC) is unknown. Aim of the study was the evaluation and distribution of LAG3 on tumour infiltrating lymphocytes (TILs) and correlation with clinico-pathological and molecular data. Methods We analysed tumor tissue samples using immunohistochemistry, multi-colour immunofluorescence and mRNA in-situ technology. The analyses were performed on a multi-spot tissue microarray (TMA) with 165 samples, followed by an evaluation on a single-spot TMA with 477 samples. These results were correlated with clinical and molecular tumour data. Results LAG3 expression on TILs was detectable in 10.5% on the multi-spot TMA and 11.4% on the single-spot TMA. There was a strong correlation between protein expression and mRNA expression (p < 0.001) in TILs. LAG 3 expression was correlated with CD4+ and CD8+ T-cells within the tumor (p < 0.001). LAG3 expression showed an improved overall survival (OS) compared to patients without LAG3 expression (median OS 70.2 vs. 26.9 months;p = 0.046). The effect was even clearer in the group of patients with tumour stages > pT2 (70.2 vs 25.0 months;p = 0.037). Conclusion This is the first description of LAG3 expression on TILs in EAC, underscoring the importance of immunomodulation in EAC. Our data suggest an impact of LAG3 in a relevant subset of EAC. Therapeutic studies investigating the efficacy of LAG3 inhibition in EAC will also provide predictive evidence and relevance of the immunohistochemical determination of LAG3 expression.
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收藏
页码:2319 / 2327
页数:9
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