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三阴性乳腺癌的免疫治疗进展。

Advances in immunotherapy for triple-negative breast cancer.

机构信息

Department of Oncology, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning Province, China.

Department of Health Management, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning Province, China.

出版信息

Mol Cancer. 2023 Sep 2;22(1):145. doi: 10.1186/s12943-023-01850-7.


DOI:10.1186/s12943-023-01850-7
PMID:37660039
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10474743/
Abstract

BACKGROUND: Immunotherapy has recently emerged as a treatment strategy which stimulates the human immune system to kill tumor cells. Tumor immunotherapy is based on immune editing, which enhances the antigenicity of tumor cells and increases the tumoricidal effect of immune cells. It also suppresses immunosuppressive molecules, activates or restores immune system function, enhances anti-tumor immune responses, and inhibits the growth f tumor cell. This offers the possibility of reducing mortality in triple-negative breast cancer (TNBC). MAIN BODY: Immunotherapy approaches for TNBC have been diversified in recent years, with breakthroughs in the treatment of this entity. Research on immune checkpoint inhibitors (ICIs) has made it possible to identify different molecular subtypes and formulate individualized immunotherapy schedules. This review highlights the unique tumor microenvironment of TNBC and integrates and analyzes the advances in ICI therapy. It also discusses strategies for the combination of ICIs with chemotherapy, radiation therapy, targeted therapy, and emerging treatment methods such as nanotechnology, ribonucleic acid vaccines, and gene therapy. Currently, numerous ongoing or completed clinical trials are exploring the utilization of immunotherapy in conjunction with existing treatment modalities for TNBC. The objective of these investigations is to assess the effectiveness of various combined immunotherapy approaches and determine the most effective treatment regimens for patients with TNBC. CONCLUSION: This review provides insights into the approaches used to overcome drug resistance in immunotherapy, and explores the directions of immunotherapy development in the treatment of TNBC.

摘要

背景:免疫疗法最近成为一种治疗策略,它可以刺激人体免疫系统杀死肿瘤细胞。肿瘤免疫疗法基于免疫编辑,它增强了肿瘤细胞的抗原性,增加了免疫细胞的杀瘤效应。它还抑制免疫抑制分子,激活或恢复免疫系统功能,增强抗肿瘤免疫反应,抑制肿瘤细胞的生长。这为降低三阴性乳腺癌(TNBC)的死亡率提供了可能。

正文:近年来,TNBC 的免疫治疗方法已经多样化,在该实体的治疗方面取得了突破。免疫检查点抑制剂(ICIs)的研究使得能够识别不同的分子亚型,并制定个体化的免疫治疗方案。这篇综述强调了 TNBC 独特的肿瘤微环境,并整合和分析了 ICI 治疗的进展。它还讨论了将 ICI 与化疗、放疗、靶向治疗以及新兴治疗方法(如纳米技术、核糖核酸疫苗和基因治疗)相结合的策略。目前,许多正在进行或已完成的临床试验正在探索免疫疗法与 TNBC 现有治疗方式联合应用的效果。这些研究的目的是评估各种联合免疫治疗方法的有效性,并确定 TNBC 患者的最佳治疗方案。

结论:本文综述了克服免疫治疗药物耐药性的方法,并探讨了免疫治疗在 TNBC 治疗中的发展方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/0b5166d4e49f/12943_2023_1850_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/a0af7159222a/12943_2023_1850_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/a4dc80cf9d03/12943_2023_1850_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/ba1f9490398c/12943_2023_1850_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/f6cd9207590b/12943_2023_1850_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/56e50b2aa796/12943_2023_1850_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/0b5166d4e49f/12943_2023_1850_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/a0af7159222a/12943_2023_1850_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/a4dc80cf9d03/12943_2023_1850_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/ba1f9490398c/12943_2023_1850_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/f6cd9207590b/12943_2023_1850_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/56e50b2aa796/12943_2023_1850_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e60/10474743/0b5166d4e49f/12943_2023_1850_Fig6_HTML.jpg

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[3]
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[4]
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引用本文的文献

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From trash to treasure: tumor draining lymph nodes as a multi-omics goldmine in cancer therapy.

Front Oncol. 2025-8-19

[2]
Molecular characterization and prognostic modeling associated with M2-like tumor-associated macrophages in breast cancer: revealing the immunosuppressive role of DLG3.

Front Immunol. 2025-8-13

[3]
H4K79 and H4K91 histone lactylation, newly identified lactylation sites enriched in breast cancer.

J Exp Clin Cancer Res. 2025-8-23

[4]
Targeting Reticulin 4 (RTN4) Within Small Extracellular Vesicles Combats Metastasis and Reinforces Immunotherapy in Triple-Negative Breast Cancer.

J Extracell Vesicles. 2025-8

[5]
Inhibition of ATM enhances the immunogenicity of triple-negative breast cancer by promoting MHC-I expression.

Cell Death Dis. 2025-8-18

[6]
Targeting LINC02544/miR-497-5p/CAPRIN1 axis via exosome-based siRNA to overcome immunotherapy resistance in triple-negative breast cancer.

Mol Med. 2025-8-16

[7]
CARG-2020 targets IL-12, IL-17, and PD-L1 pathways to effectively treat melanoma and breast cancer.

Sci Rep. 2025-8-13

[8]
Application of Immune Checkpoint Inhibitors in Cancer.

MedComm (2020). 2025-8-10

[9]
TIGIT, as a potential immune checkpoint target for immunotherapy of breast cancer.

Med Oncol. 2025-8-5

[10]
An immunomodulatory photosensitizer-mediated photodynamic therapy synergizes with PD-L1 blockade against metastatic triple-negative breast cancer.

Front Pharmacol. 2025-7-17

本文引用的文献

[1]
Combination of FAK inhibitor and cytokine-induced killer cell therapy: An alternative therapeutic strategy for patients with triple-negative breast cancer.

Biomed Pharmacother. 2023-7

[2]
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Biomed Pharmacother. 2023-7

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Sci Transl Med. 2023-3-8

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Front Cell Dev Biol. 2023-1-30

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Sci Adv. 2023-1-13

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Nat Commun. 2022-11-2

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J Control Release. 2022-11

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A tumor cell membrane-coated self-amplified nanosystem as a nanovaccine to boost the therapeutic effect of anti-PD-L1 antibody.

Bioact Mater. 2022-9-13

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