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增强CD8 T细胞的抗肿瘤免疫力:一种改善晚期前列腺癌治疗反应的有前景的策略。

Bolstering CD8 T Cells' Antitumor Immunity: A Promising Strategy to Improve the Response to Advanced Prostate Cancer Treatment.

作者信息

Dang Beijing, Liang Lixin, Li Zhijun, Luo Junli, Zhong Shangwei

机构信息

The Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang 421009, China.

出版信息

Biology (Basel). 2025 May 14;14(5):544. doi: 10.3390/biology14050544.

DOI:10.3390/biology14050544
PMID:40427733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12108615/
Abstract

Prostate cancer is among the most frequently diagnosed and deadly cancers among men in the Western world. It is typically classified as an immune "cold" tumor due to its sparse immune cell presence and limited immunogenic response. Recent research has revealed the significant role of immune cells, especially CD8 T cells, in both prostate cancer progression and treatment efficacy. This review integrates recent findings to provide a comprehensive overview of the current understanding of CD8 T cell dynamics in prostate cancer and discusses emerging strategies to improve treatment outcomes. The ongoing exploration of new molecular targets and the development of innovative immunotherapeutic approaches hold promise for more effective management of prostate cancer, particularly in the context of advanced and resistant forms of the disease.

摘要

前列腺癌是西方世界男性中最常被诊断出且致命的癌症之一。由于其免疫细胞数量稀少且免疫原性反应有限,它通常被归类为免疫“冷”肿瘤。最近的研究揭示了免疫细胞,尤其是CD8 T细胞,在前列腺癌进展和治疗效果中的重要作用。本综述整合了近期的研究结果,全面概述了目前对前列腺癌中CD8 T细胞动态的理解,并讨论了改善治疗结果的新兴策略。对新分子靶点的持续探索和创新免疫治疗方法的开发,有望更有效地管理前列腺癌,特别是在该疾病的晚期和耐药形式的背景下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2976/12108615/01f5e01e82a4/biology-14-00544-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2976/12108615/edf35a1d7ef5/biology-14-00544-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2976/12108615/0832f550f64b/biology-14-00544-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2976/12108615/01f5e01e82a4/biology-14-00544-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2976/12108615/edf35a1d7ef5/biology-14-00544-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2976/12108615/0832f550f64b/biology-14-00544-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2976/12108615/01f5e01e82a4/biology-14-00544-g003.jpg

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本文引用的文献

1
Pembrolizumab Plus Docetaxel Versus Docetaxel for Previously Treated Metastatic Castration-Resistant Prostate Cancer: The Randomized, Double-Blind, Phase III KEYNOTE-921 Trial.帕博利珠单抗联合多西他赛对比多西他赛用于既往治疗过的转移性去势抵抗性前列腺癌:随机、双盲、III期KEYNOTE-921试验
J Clin Oncol. 2025 May 10;43(14):1638-1649. doi: 10.1200/JCO-24-01283. Epub 2025 Mar 5.
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Evolution of myeloid-mediated immunotherapy resistance in prostate cancer.前列腺癌中髓系介导的免疫治疗耐药性的演变
Nature. 2025 Jan;637(8048):1207-1217. doi: 10.1038/s41586-024-08290-3. Epub 2024 Dec 4.
3
Reduction of myeloid-derived suppressor cells in prostate cancer murine models and patients following white button mushroom treatment.
白蘑菇处理后前列腺癌小鼠模型和患者中髓源性抑制细胞的减少。
Clin Transl Med. 2024 Oct;14(10):e70048. doi: 10.1002/ctm2.70048.
4
The Immune Microenvironment in Prostate Cancer: A Comprehensive Review.前列腺癌中的免疫微环境:综述
Oncology. 2024 Oct 9:1-25. doi: 10.1159/000541881.
5
Intrinsic ADRB2 inhibition improves CAR-T cell therapy efficacy against prostate cancer.内在 ADRB2 抑制可提高 CAR-T 细胞疗法治疗前列腺癌的疗效。
Mol Ther. 2024 Oct 2;32(10):3539-3557. doi: 10.1016/j.ymthe.2024.08.028. Epub 2024 Sep 2.
6
YAP1 Inhibition Induces Phenotype Switching of Cancer-Associated Fibroblasts to Tumor Suppressive in Prostate Cancer.YAP1 抑制诱导前列腺癌中癌相关成纤维细胞向肿瘤抑制表型的转变。
Cancer Res. 2024 Nov 15;84(22):3728-3742. doi: 10.1158/0008-5472.CAN-24-0932.
7
Comprehensive investigation in oncogenic functions and immunological roles of NCBP2 and its validation in prostate cancer.NCBP2致癌功能及免疫作用的综合研究及其在前列腺癌中的验证
Transl Oncol. 2024 Sep;47:102049. doi: 10.1016/j.tranon.2024.102049. Epub 2024 Jul 3.
8
Microsatellite Instability, Tumor Mutational Burden, and Response to Immune Checkpoint Blockade in Patients with Prostate Cancer.前列腺癌患者的微卫星不稳定性、肿瘤突变负担与免疫检查点阻断治疗反应
Clin Cancer Res. 2024 Sep 3;30(17):3894-3903. doi: 10.1158/1078-0432.CCR-23-3403.
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PSCA-CAR T cell therapy in metastatic castration-resistant prostate cancer: a phase 1 trial.PSCA-CAR T 细胞疗法治疗转移性去势抵抗性前列腺癌:一项 1 期试验。
Nat Med. 2024 Jun;30(6):1636-1644. doi: 10.1038/s41591-024-02979-8. Epub 2024 Jun 12.
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J Exp Clin Cancer Res. 2024 May 23;43(1):149. doi: 10.1186/s13046-024-03063-2.