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免疫抑制性肿瘤微环境与肝细胞癌的免疫治疗:现状与展望。

Immunosuppressive tumor microenvironment and immunotherapy of hepatocellular carcinoma: current status and prospectives.

机构信息

Hepatobiliary Surgery, Department of General Surgery, Huashan Hospital & Cancer Metastasis Institute, Fudan University, 12 Urumqi Road (M), Shanghai, 200040, China.

Institutes of Biomedical Sciences, Fudan University, Shanghai, 200032, China.

出版信息

J Hematol Oncol. 2024 Apr 29;17(1):25. doi: 10.1186/s13045-024-01549-2.


DOI:10.1186/s13045-024-01549-2
PMID:38679698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11057182/
Abstract

Hepatocellular carcinoma (HCC) is a major health concern worldwide, with limited therapeutic options and poor prognosis. In recent years, immunotherapies such as immune checkpoint inhibitors (ICIs) have made great progress in the systemic treatment of HCC. The combination treatments based on ICIs have been the major trend in this area. Recently, dual immune checkpoint blockade with durvalumab plus tremelimumab has also emerged as an effective treatment for advanced HCC. However, the majority of HCC patients obtain limited benefits. Understanding the immunological rationale and exploring novel ways to improve the efficacy of immunotherapy has drawn much attention. In this review, we summarize the latest progress in this area, the ongoing clinical trials of immune-based combination therapies, as well as novel immunotherapy strategies such as chimeric antigen receptor T cells, personalized neoantigen vaccines, oncolytic viruses, and bispecific antibodies.

摘要

肝细胞癌(HCC)是全球范围内的一个主要健康关注点,治疗选择有限,预后较差。近年来,免疫疗法(如免疫检查点抑制剂[ICIs])在 HCC 的系统治疗方面取得了重大进展。基于 ICIs 的联合治疗已成为该领域的主要趋势。最近,度伐利尤单抗联合替西木单抗的双重免疫检查点阻断也已成为晚期 HCC 的一种有效治疗方法。然而,大多数 HCC 患者获益有限。了解免疫学原理并探索提高免疫疗法疗效的新方法引起了广泛关注。在这篇综述中,我们总结了这一领域的最新进展,包括正在进行的免疫联合治疗临床试验,以及嵌合抗原受体 T 细胞、个性化新抗原疫苗、溶瘤病毒和双特异性抗体等新型免疫疗法策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48d9/11057182/b6a718b99f03/13045_2024_1549_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48d9/11057182/3ae8659d2654/13045_2024_1549_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48d9/11057182/b6a718b99f03/13045_2024_1549_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48d9/11057182/3ae8659d2654/13045_2024_1549_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48d9/11057182/b6a718b99f03/13045_2024_1549_Fig2_HTML.jpg

相似文献

[1]
Immunosuppressive tumor microenvironment and immunotherapy of hepatocellular carcinoma: current status and prospectives.

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[2]
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[4]
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[6]
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[8]
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引用本文的文献

[1]
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BMC Med Imaging. 2025-9-1

[2]
Targeting Glypican-3 for Liver Cancer Therapy: Clinical Applications and Detection Methods.

J Clin Transl Hepatol. 2025-8-28

[3]
The efficacy and safety of immune combination therapy in patients with driver gene-negative non-small cell lung cancer with liver metastasis: a systematic review and network meta-analysis.

BMC Cancer. 2025-8-18

[4]
Decoding the tumor microenvironment: insights into immunotherapy and beyond.

J Natl Cancer Cent. 2025-4-28

[5]
Beyond borders: engineering organ-targeted immunotherapies to overcome site-specific barriers in cancer.

Drug Deliv Transl Res. 2025-8-11

[6]
Advances in mechanisms and challenges in clinical translation of synergistic nanomaterial-based therapies for melanoma.

Front Cell Dev Biol. 2025-7-25

[7]
NOX1 inhibition sensitizes HCC cells to sorafenib and radiotherapy by modulating ROS-mediated programmed cell death.

Acta Pharmacol Sin. 2025-8-7

[8]
Prognostic and immunotherapeutic response prediction in hepatocellular carcinoma: role of non-histone acetylation/deacetylation scoring.

Discov Oncol. 2025-8-7

[9]
Near-infrared-triggered copper-doped carbon nitride nanocomposite inducing domino effect for synergistic tumor therapy and immune microenvironment reprogramming.

Mater Today Bio. 2025-7-25

[10]
Matching-adjusted indirect comparison of tislelizumab plus lenvatinib versus sintilimab plus bevacizumab biosimilar as first-line treatment for unresectable hepatocellular carcinoma.

Front Immunol. 2025-6-23

本文引用的文献

[1]
Regulation and impact of tumor-specific CD4 T cells in cancer and immunotherapy.

Trends Immunol. 2024-4

[2]
Cirrhotic-extracellular matrix attenuates aPD-1 treatment response by initiating immunosuppressive neutrophil extracellular traps formation in hepatocellular carcinoma.

Exp Hematol Oncol. 2024-2-22

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Pathogenic Th17 cell-mediated liver fibrosis contributes to resistance to PD-L1 antibody immunotherapy in hepatocellular carcinoma.

Int Immunopharmacol. 2024-3-10

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Nat Med. 2024-3

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Lancet Oncol. 2023-12

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J Hepatol. 2023-12

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RUNX-3-expressing CAR T cells targeting glypican-3 in patients with heavily pretreated advanced hepatocellular carcinoma: a phase I trial.

EClinicalMedicine. 2023-8-30

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