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可溶性程序性死亡配体1:从免疫逃逸到癌症治疗

Soluble PD-L1: From Immune Evasion to Cancer Therapy.

作者信息

Dragu Denisa, Necula Laura Georgiana, Bleotu Coralia, Diaconu Carmen C, Chivu-Economescu Mihaela

机构信息

Stefan S. Nicolau Institute of Virology, 030304 Bucharest, Romania.

Faculty of Medicine, Titu Maiorescu University, 031593 Bucharest, Romania.

出版信息

Life (Basel). 2025 Apr 8;15(4):626. doi: 10.3390/life15040626.

DOI:10.3390/life15040626
PMID:40283180
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12028844/
Abstract

Immunotherapy has emerged as a promising approach to cancer treatment, but only a small percentage of cancer patients benefit from it. To enhance therapeutic outcomes, it is essential to understand factors influencing immune response and tumor progression. Soluble PD-L1 (sPD-L1) has been identified as an essential element in immune regulation, with potential implications in cancer biology and treatment. This manuscript explores the sources and mechanisms of sPD-L1 production, its role in immune evasion and tumor progression, and its clinical significance. Elevated sPD-L1 levels have been linked to disease severity, survival, and treatment response in various malignancies, and as a consequence, strategies for combinatorial targeting of sPD-L1 with other immunotherapies are considered. Further studies are needed to understand sPD-L1 dynamics and to clarify the mechanisms of sPD-L1-mediated immunosuppression and its therapeutic implications.

摘要

免疫疗法已成为一种很有前景的癌症治疗方法,但只有一小部分癌症患者能从中受益。为提高治疗效果,了解影响免疫反应和肿瘤进展的因素至关重要。可溶性程序性死亡配体1(sPD-L1)已被确定为免疫调节中的一个关键要素,对癌症生物学和治疗具有潜在影响。本文探讨了sPD-L1的产生来源和机制、其在免疫逃逸和肿瘤进展中的作用及其临床意义。sPD-L1水平升高与多种恶性肿瘤的疾病严重程度、生存率和治疗反应相关,因此,考虑将sPD-L1与其他免疫疗法联合靶向治疗的策略。需要进一步研究来了解sPD-L1的动态变化,并阐明sPD-L1介导的免疫抑制机制及其治疗意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69f4/12028844/1e7f0b33d932/life-15-00626-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69f4/12028844/bc7052180cbd/life-15-00626-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69f4/12028844/1e7f0b33d932/life-15-00626-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69f4/12028844/bc7052180cbd/life-15-00626-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69f4/12028844/1e7f0b33d932/life-15-00626-g002.jpg

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Mol Ther. 2024 Dec 4;32(12):4235-4255. doi: 10.1016/j.ymthe.2024.09.026. Epub 2024 Sep 28.
2
Targeting PD-1/PD-L-1 immune checkpoint inhibition for cancer immunotherapy: success and challenges.靶向PD-1/PD-L-1免疫检查点抑制用于癌症免疫治疗:成功与挑战
Front Immunol. 2024 Apr 10;15:1383456. doi: 10.3389/fimmu.2024.1383456. eCollection 2024.
3
Soluble immune checkpoint factors reflect exhaustion of antitumor immunity and response to PD-1 blockade.
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J Clin Invest. 2024 Apr 1;134(7):e168318. doi: 10.1172/JCI168318.
4
The combination of soluble forms of PD-1 and PD-L1 as a predictive marker of PD-1 blockade in patients with advanced cancers: a multicenter retrospective study.可溶性 PD-1 和 PD-L1 联合作为预测晚期癌症患者 PD-1 阻断疗效的标志物:一项多中心回顾性研究。
Front Immunol. 2023 Dec 11;14:1325462. doi: 10.3389/fimmu.2023.1325462. eCollection 2023.
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