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宫颈癌肿瘤微环境中的T细胞亚群:进展与治疗机遇

T cell subsets in cervical cancer tumor microenvironment: advances and therapeutic opportunities.

作者信息

Guo Weilin, Dai Lan, Qiu Lihua

机构信息

Department of Obstetrics and Gynecology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Shanghai Key Laboratory of Gynecologic Oncology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Front Immunol. 2025 Jun 5;16:1612032. doi: 10.3389/fimmu.2025.1612032. eCollection 2025.

DOI:10.3389/fimmu.2025.1612032
PMID:40539072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12176900/
Abstract

Cervical cancer is the third most common malignancy among Chinese women in both incidence and mortality. Its progression is closely linked to complex interactions among immune cells within the tumor microenvironment (TME). As key components of the immune landscape, different T cell subsets play diverse and dynamic roles in shaping tumor immunity. This review provides a comprehensive overview of the roles of various T cell subsets in the TME of cervical cancer, with a focus on their distribution, functional heterogeneity, dynamic balance, and variations across different pathological subtypes and disease stages. We also highlight the intricate crosstalk between T cells and other immune cells in the TME and discuss recent advances in T cell-related immunotherapies for cervical cancer, including immune checkpoint inhibitors and HPV-targeted vaccines. By elucidating the roles of distinct T cell subsets and relevant immunotherapeutic approaches within the TME, this review provides insights into potential therapeutic targets and approaches for improving cervical cancer treatment and patient outcome.

摘要

宫颈癌是中国女性中发病率和死亡率均位列第三的常见恶性肿瘤。其进展与肿瘤微环境(TME)内免疫细胞之间的复杂相互作用密切相关。作为免疫格局的关键组成部分,不同的T细胞亚群在塑造肿瘤免疫方面发挥着多样且动态的作用。本综述全面概述了各种T细胞亚群在宫颈癌TME中的作用,重点关注它们的分布、功能异质性、动态平衡以及在不同病理亚型和疾病阶段的变化。我们还强调了TME中T细胞与其他免疫细胞之间的复杂相互作用,并讨论了宫颈癌T细胞相关免疫疗法的最新进展,包括免疫检查点抑制剂和HPV靶向疫苗。通过阐明TME中不同T细胞亚群的作用及相关免疫治疗方法,本综述为改善宫颈癌治疗和患者预后的潜在治疗靶点及方法提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4753/12176900/0f5866fe0dae/fimmu-16-1612032-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4753/12176900/4f1fa1837912/fimmu-16-1612032-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4753/12176900/0f5866fe0dae/fimmu-16-1612032-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4753/12176900/4f1fa1837912/fimmu-16-1612032-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4753/12176900/0f5866fe0dae/fimmu-16-1612032-g002.jpg

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本文引用的文献

1
Hyperactivity of the IL-33-ILC2s-IL-13-M-MDSCs axis promotes cervical cancer progression.IL-33-ILC2s-IL-13-M-MDSCs轴的过度活跃促进宫颈癌进展。
Int Immunopharmacol. 2025 Jan 10;144:113693. doi: 10.1016/j.intimp.2024.113693. Epub 2024 Nov 29.
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The prognostic value of Th17/Treg cell in cervical cancer: a systematic review and meta-analysis.Th17/Treg细胞在宫颈癌中的预后价值:一项系统评价与荟萃分析。
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Integrating Single-Cell RNA-Seq and Bulk RNA-Seq to Construct a Novel γδT Cell-Related Prognostic Signature for Human Papillomavirus-Infected Cervical Cancer.
整合单细胞 RNA-Seq 和批量 RNA-Seq 构建新型人乳头瘤病毒感染宫颈癌 γδT 细胞相关预后标志物。
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STING agonist inflames the cervical cancer immune microenvironment and overcomes anti-PD-1 therapy resistance.STING 激动剂激活宫颈癌免疫微环境并克服抗 PD-1 治疗耐药性。
Front Immunol. 2024 Mar 14;15:1342647. doi: 10.3389/fimmu.2024.1342647. eCollection 2024.
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The immune microenvironment of cancer of the uterine cervix.宫颈癌的免疫微环境。
Histol Histopathol. 2024 Oct;39(10):1245-1271. doi: 10.14670/HH-18-727. Epub 2024 Mar 1.
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Tumor immunity: A brief overview of tumor‑infiltrating immune cells and research advances into tumor‑infiltrating lymphocytes in gynecological malignancies (Review).肿瘤免疫:肿瘤浸润免疫细胞概述及妇科恶性肿瘤中肿瘤浸润淋巴细胞的研究进展(综述)
Exp Ther Med. 2024 Feb 26;27(4):166. doi: 10.3892/etm.2024.12453. eCollection 2024 Apr.
7
Multiomics profiling reveals the benefits of gamma-delta (γδ) T lymphocytes for improving the tumor microenvironment, immunotherapy efficacy and prognosis in cervical cancer.多组学分析揭示了 γδ T 淋巴细胞改善宫颈癌肿瘤微环境、免疫治疗疗效和预后的作用。
J Immunother Cancer. 2024 Jan 9;12(1):e008355. doi: 10.1136/jitc-2023-008355.
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immunotherapy engineered with highly efficient tumor antigen coating establishes antigen-specific CD8+ T cell immunity and increases in antitumor efficacy with type I interferon combination therapy.用高效肿瘤抗原包被工程改造的免疫疗法可建立抗原特异性 CD8+ T 细胞免疫,并与 I 型干扰素联合治疗增加抗肿瘤疗效。
Oncoimmunology. 2023 Dec 27;13(1):2298444. doi: 10.1080/2162402X.2023.2298444. eCollection 2024.
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Rebalancing TGF-β/PGE breaks RT-induced immunosuppressive barriers by enhancing tumor-infiltrated dendritic cell homing.重新平衡 TGF-β/PGE 通过增强肿瘤浸润树突状细胞归巢打破 RT 诱导的免疫抑制屏障。
Int J Biol Sci. 2024 Jan 1;20(1):367-386. doi: 10.7150/ijbs.87867. eCollection 2024.
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IL-10CD19 regulatory B cells induce CD4Foxp3regulatory T cells in serum of cervical cancer patients.白细胞介素-10 CD19 调节性 B 细胞在宫颈癌患者血清中诱导 CD4Foxp3 调节性 T 细胞。
Autoimmunity. 2024 Dec;57(1):2290909. doi: 10.1080/08916934.2023.2290909. Epub 2023 Dec 12.