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肝细胞癌免疫微环境中树突状细胞的研究进展。

Research Progress on Dendritic Cells in Hepatocellular Carcinoma Immune Microenvironments.

机构信息

The Affiliated Taizhou People's Hospital of Nanjing Medical University, Taizhou 225300, China.

Graduate School, Nanjing University of Chinese Medicine, Nanjing 210023, China.

出版信息

Biomolecules. 2024 Sep 16;14(9):1161. doi: 10.3390/biom14091161.


DOI:10.3390/biom14091161
PMID:39334927
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11430656/
Abstract

Dendritic cells (DCs) are antigen-presenting cells that play a crucial role in initiating immune responses by cross-presenting relevant antigens to initial T cells. The activation of DCs is a crucial step in inducing anti-tumor immunity. Upon recognition and uptake of tumor antigens, activated DCs present these antigens to naive T cells, thereby stimulating T cell-mediated immune responses and enhancing their ability to attack tumors. It is particularly noted that DCs are able to cross-present foreign antigens to major histocompatibility complex class I (MHC-I) molecules, prompting CD8 T cells to proliferate and differentiate into cytotoxic T cells. In the malignant progression of hepatocellular carcinoma (HCC), the inactivation of DCs plays an important role, and the activation of DCs is particularly important in anti-HCC immunotherapy. In this review, we summarize the mechanisms of DCs activation in HCC, the involved regulatory factors and strategies to activate DCs in HCC immunotherapy. It provides a basis for the study of HCC immunotherapy through DCs activation.

摘要

树突状细胞(DCs)是抗原呈递细胞,通过将相关抗原交叉呈递给初始 T 细胞,在启动免疫反应中发挥着关键作用。DCs 的激活是诱导抗肿瘤免疫的关键步骤。在识别和摄取肿瘤抗原后,激活的 DCs 将这些抗原呈递给初始 T 细胞,从而刺激 T 细胞介导的免疫反应,并增强其攻击肿瘤的能力。值得注意的是,DCs 能够将外源抗原交叉呈递给主要组织相容性复合体 I 类(MHC-I)分子,促使 CD8 T 细胞增殖并分化为细胞毒性 T 细胞。在肝细胞癌(HCC)的恶性进展中,DCs 的失活起着重要作用,而激活 DCs 在 HCC 免疫治疗中尤为重要。本综述总结了 HCC 中 DCs 激活的机制、涉及的调节因子以及在 HCC 免疫治疗中激活 DCs 的策略,为通过 DCs 激活研究 HCC 免疫治疗提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f2/11430656/810bb2e9fbc1/biomolecules-14-01161-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f2/11430656/9b3fff4bf343/biomolecules-14-01161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f2/11430656/810bb2e9fbc1/biomolecules-14-01161-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f2/11430656/9b3fff4bf343/biomolecules-14-01161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f2/11430656/810bb2e9fbc1/biomolecules-14-01161-g002.jpg

相似文献

[1]
Research Progress on Dendritic Cells in Hepatocellular Carcinoma Immune Microenvironments.

Biomolecules. 2024-9-16

[2]
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[3]
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[4]
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Int J Mol Med. 2013-9-27

[5]
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J Transl Med. 2008-9-15

[6]
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[7]
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[8]
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Cell Mol Immunol. 2006-6

[9]
[Inducing hepatocellular carcinoma-specific cytotoxic T lymphocyte response using formed by fusion of FastDCs and allogeneic human hepatocellular carcinoma cells].

Zhonghua Yi Xue Za Zhi. 2005-12-14

[10]
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引用本文的文献

[1]
Exploring the impact of galectins on liver cancer: From immunopathogenesis to potential targets.

World J Gastroenterol. 2025-7-7

[2]
Harnessing Dendritic Cell Function in Hepatocellular Carcinoma: Advances in Immunotherapy and Therapeutic Strategies.

Vaccines (Basel). 2025-5-4

[3]
Focusing on DC cells to optimize the prediction of prognosis and innovative treatment strategies for colon cancer.

Sci Rep. 2025-5-19

[4]
Advancing precision medicine in hepatocellular carcinoma: current challenges and future directions in liquid biopsy, immune microenvironment, single nucleotide polymorphisms, and conversion therapy.

Hepat Oncol. 2025-12

[5]
The Malignant Transformation of Viral Hepatitis to Hepatocellular Carcinoma: Mechanisms and Interventions.

MedComm (2020). 2025-3-8

[6]
Emerging Mechanisms and Biomarkers Associated with T-Cells and B-Cells in Autoimmune Disorders.

Clin Rev Allergy Immunol. 2025-2-11

本文引用的文献

[1]
EGR1 suppresses HCC growth and aerobic glycolysis by transcriptionally downregulating PFKL.

J Exp Clin Cancer Res. 2024-1-29

[2]
In Situ Nanofiber Patch Boosts Postoperative Hepatocellular Carcinoma Immune Activation by Trimodal Combination Therapy.

ACS Nano. 2024-1-9

[3]
Identification of subclusters and prognostic genes based on glycolysis/gluconeogenesis in hepatocellular carcinoma.

Front Immunol. 2023

[4]
Autophagy-amplifying nanoparticles evoke immunogenic cell death combined with anti-PD-1/PD-L1 for residual tumors immunotherapy after RFA.

J Nanobiotechnology. 2023-10-3

[5]
A Booster for Radiofrequency Ablation: Advanced Adjuvant Therapy via Nanovaccine Synergized with Anti-programmed Death Ligand 1 Immunotherapy for Systemically Constraining Hepatocellular Carcinoma.

ACS Nano. 2023-10-10

[6]
Synergistic efficacy of simultaneous anti-TGF-β/VEGF bispecific antibody and PD-1 blockade in cancer therapy.

J Hematol Oncol. 2023-8-12

[7]
Caveolin-mediated cytosolic delivery of spike nanoparticle enhances antitumor immunity of neoantigen vaccine for hepatocellular carcinoma.

Theranostics. 2023

[8]
New techniques: a roadmap for the development of HCC immunotherapy.

Front Immunol. 2023

[9]
Abrine, an IDO1 inhibitor, suppresses the immune escape and enhances the immunotherapy of anti-PD-1 antibody in hepatocellular carcinoma.

Front Immunol. 2023

[10]
Activation, Amplification, and Ablation as Dynamic Mechanisms of Dendritic Cell Maturation.

Biology (Basel). 2023-5-14

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