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胆管癌的免疫学和免疫疗法。

Immunology and immunotherapy of cholangiocarcinoma.

机构信息

Gastrointestinal Malignancies Section, Thoracic and Gastrointestinal Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Liver Cancer Program, Bethesda, MD, USA.

出版信息

Nat Rev Gastroenterol Hepatol. 2023 Jun;20(6):349-365. doi: 10.1038/s41575-022-00741-4. Epub 2023 Jan 25.


DOI:10.1038/s41575-022-00741-4
PMID:36697706
Abstract

Cholangiocarcinoma is the second most common primary liver cancer. Its incidence is low in the Western world but is rising globally. Surgery, chemotherapy and radiation therapy have been the only treatment options for decades. Progress in our molecular understanding of the disease and the identification of druggable targets, such as IDH1 mutations and FGFR2 fusions, has provided new treatment options. Immunotherapy has emerged as a potent strategy for many different types of cancer and has shown efficacy in combination with chemotherapy for cholangiocarcinoma. In this Review, we discuss findings related to key immunological aspects of cholangiocarcinoma, including the heterogeneous landscape of immune cells within the tumour microenvironment, the immunomodulatory effect of the microbiota and IDH1 mutations, and the association of immune-related signatures and patient outcomes. We introduce findings from preclinical immunotherapy studies, discuss future immune-mediated treatment options, and provide a summary of results from clinical trials testing immune-based approaches in patients with cholangiocarcinoma. This Review provides a thorough survey of our knowledge on immune signatures and immunotherapy in cholangiocarcinoma.

摘要

胆管癌是第二常见的原发性肝癌。在西方世界,其发病率较低,但在全球范围内呈上升趋势。几十年来,手术、化疗和放疗一直是唯一的治疗选择。我们对该疾病分子机制的理解的进步,以及对可用药靶的识别,如 IDH1 突变和 FGFR2 融合,为提供了新的治疗选择。免疫疗法已成为许多不同类型癌症的有效治疗策略,并在胆管癌中显示出与化疗联合的疗效。在这篇综述中,我们讨论了与胆管癌的关键免疫学方面相关的发现,包括肿瘤微环境中免疫细胞的异质性、微生物群和 IDH1 突变的免疫调节作用,以及与免疫相关的特征和患者预后的关联。我们介绍了临床前免疫治疗研究的结果,讨论了未来的免疫介导治疗选择,并总结了临床试验结果,这些试验检测了免疫治疗方法在胆管癌患者中的应用。这篇综述对我们在胆管癌中的免疫特征和免疫治疗方面的知识进行了全面的调查。

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引用本文的文献

[1]
Immunological Landscape and Molecular Therapeutic Targets of the Tumor Microenvironment in Hepatocellular Carcinoma.

Int J Mol Sci. 2025-8-13

[2]
Clinical and translational study of ivosidenib plus nivolumab in advanced solid tumors harboring IDH1 mutations.

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[3]
PTP4A1 promotes intrahepatic cholangiocarcinoma development and progression by interacting with PTEN and activating the PI3K/AKT/GSKα axis.

Oncol Rep. 2025-10

[4]
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[5]
Myeloid cells in chronic liver inflammation.

Cell Mol Immunol. 2025-7-28

[6]
Association of α-SMA/FAP-positive cancer-associated fibroblasts with clinicopathological features and prognosis in extrahepatic cholangiocarcinoma.

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[7]
The DCDC2/ENO1 axis promotes tumor progression and immune evasion in intrahepatic cholangiocarcinoma via activating FGL1-LAG3 checkpoint.

J Exp Clin Cancer Res. 2025-6-18

[8]
NCAPG2 is a diagnostic biomarker associated with immune infiltration in cholangiocarcinoma.

Discov Oncol. 2025-5-30

[9]
Prognosis of cholangiocarcinoma patients based on multiple patterns of programmed cell death, integrated analysis of the immune microenvironment and drug sensitivity.

Front Genet. 2025-5-14

[10]
Causal role of immune cells in primary liver cancer: a mendelian randomization study.

BMC Cancer. 2025-5-23

本文引用的文献

[1]
Gut-liver axis: Pathophysiological concepts and clinical implications.

Cell Metab. 2022-11-1

[2]
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Nature. 2022-10

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Cell Rep. 2022-9-20

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Cancer Immunol Res. 2022-7-1

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Regulatory T cells induce a suppressive immune milieu and promote lymph node metastasis in intrahepatic cholangiocarcinoma.

Br J Cancer. 2022-9

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Gut. 2023-4

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Gut. 2022-8

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CXCR2 inhibition enables NASH-HCC immunotherapy.

Gut. 2022-4-27

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EGFR Inhibition Potentiates FGFR Inhibitor Therapy and Overcomes Resistance in FGFR2 Fusion-Positive Cholangiocarcinoma.

Cancer Discov. 2022-5-2

[10]
Combination gemcitabine and PD-L1xCD3 bispecific T cell engager (BiTE) enhances T lymphocyte cytotoxicity against cholangiocarcinoma cells.

Sci Rep. 2022-4-13

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