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早期肝损伤呈现幼稚三级淋巴结构,并表现出免疫抑制和免疫抑制分子的高表达。

Early Hepatic Lesions Display Immature Tertiary Lymphoid Structures and Show Elevated Expression of Immune Inhibitory and Immunosuppressive Molecules.

机构信息

Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, USPC, Université de Paris, Inflammation, Complement and Cancer Team, Paris, France.

Programme Cartes d'Identité des Tumeurs, Ligue Nationale Contre le Cancer, Paris, France.

出版信息

Clin Cancer Res. 2020 Aug 15;26(16):4381-4389. doi: 10.1158/1078-0432.CCR-19-2929. Epub 2020 Apr 8.

Abstract

PURPOSE

The impact of tertiary lymphoid structures (TLS) in hepatocellular carcinoma (HCC) progression is being extensively investigated. However, their presence during the early steps of human liver carcinogenesis remains unknown. We thus aimed to determine whether TLS are induced in preneoplastic/early hepatic lesions (EHL), and whether they are associated with a particular immune profile.

EXPERIMENTAL DESIGN

A series of 127 EHLs (low/high-grade dysplastic nodules, early HCC, and small and progressed HCC) was included in the study. TLSs were investigated by pathologic reviewing. Densities of immune cells were assessed using IHC. A subset of lesions was microdissected and gene expression profiling was performed with a custom NanoString panel.

RESULTS

Compared with surrounding cirrhotic nodules, EHL of all stages displayed increased densities of T cells, B cells, and dendritic cells. Immature TLSs were identified in 24% of EHL. Gene expression profiling identified a subset of EHL with elevated mRNA levels of various cytokines involved in immune cells' recruitment and TLS induction. This subgroup of EHL also showed overexpression of genes related to T- and B-cells' activation and antigen presentation, as well as those related to immunosuppression and immune exhaustion.

CONCLUSIONS

Local immune activation occurs in the very early steps of liver carcinogenesis; however, it may not be fully efficient and paradoxically favor immune evasion and progression to full-blown HCC. These results have implications for the development of anti-HCC chemopreventive strategies in cirrhotic patients.

摘要

目的

三级淋巴结构(TLS)在肝细胞癌(HCC)进展中的作用正在被广泛研究。然而,它们在人类肝癌发生的早期阶段的存在仍然未知。因此,我们旨在确定 TLS 是否在癌前/早期肝病变(EHL)中诱导产生,以及它们是否与特定的免疫特征相关。

实验设计

本研究纳入了 127 例 EHL(低/高级别异型增生结节、早期 HCC 和小 HCC 及进展期 HCC)。通过病理复查来研究 TLS。使用 IHC 评估免疫细胞密度。对一部分病变进行微切割,并使用定制的 NanoString 面板进行基因表达谱分析。

结果

与周围肝硬化结节相比,所有阶段的 EHL 中 T 细胞、B 细胞和树突状细胞的密度均增加。在 24%的 EHL 中发现了不成熟的 TLS。基因表达谱分析确定了一组 EHL 的各种细胞因子的 mRNA 水平升高,这些细胞因子参与免疫细胞的募集和 TLS 的诱导。这组 EHL 还表现出与 T 细胞和 B 细胞激活和抗原呈递相关的基因的过度表达,以及与免疫抑制和免疫衰竭相关的基因的过度表达。

结论

局部免疫激活发生在肝癌发生的早期阶段;然而,它可能不完全有效,反而有利于免疫逃避和进展为完全成熟的 HCC。这些结果对肝硬化患者开发抗 HCC 化学预防策略具有重要意义。

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