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髓源性抑制细胞在肝癌中的作用。

The role of myeloid-derived suppressor cells in liver cancer.

作者信息

Zhou Shiyue, Zhao Zixuan, Zhong Hao, Ren Zehao, Li Yuye, Wang Hong, Qiu Yuling

机构信息

State Key Laboratory of Component-based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, 10 Poyanghu Road, Jinghai District, Tianjin, 301617, People's Republic of China.

School of Medical Technology, Tianjin University of Traditional Chinese Medicine, 10 Poyanghu Rd., West Area, Tuanbo New Town, Jinghai Dist, Tianjin, 301617, China.

出版信息

Discov Oncol. 2023 May 23;14(1):77. doi: 10.1007/s12672-023-00681-8.

DOI:10.1007/s12672-023-00681-8
PMID:37217620
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10203092/
Abstract

MDSCs are immature myeloid immune cells, which accumulate in models of liver cancer to reduce effector immune cell activity, contribute to immune escape and treatment resistance. The accumulation of MDSCs suppresses the role of CTL and the killing effects of NK cells, induces the accumulation of Treg cells, and blocks the antigen presentation of DCs, thus promoting the progression of liver cancer. Recently, immunotherapy has emerged a valuable approach following chemoradiotherapy in the therapy of advanced liver cancer. A considerable increasing of researches had proved that targeting MDSCs has become one of the therapeutic targets to enhance tumor immunity. In preclinical study models, targeting MDSCs have shown encouraging results in both alone and in combination administration. In this paper, we elaborated immune microenvironment of the liver, function and regulatory mechanisms of MDSCs, and therapeutic approaches to target MDSCs. We also expect these strategies to supply new views for future immunotherapy for the treatment of liver cancer.

摘要

髓源性抑制细胞(MDSCs)是未成熟的髓系免疫细胞,在肝癌模型中会积累,以降低效应免疫细胞的活性,导致免疫逃逸和治疗抵抗。MDSCs的积累会抑制细胞毒性T淋巴细胞(CTL)的作用和自然杀伤(NK)细胞的杀伤效应,诱导调节性T细胞(Treg细胞)的积累,并阻断树突状细胞(DCs)的抗原呈递,从而促进肝癌的进展。近年来,免疫疗法已成为晚期肝癌放化疗后的一种有价值的治疗方法。大量研究已证明,靶向MDSCs已成为增强肿瘤免疫的治疗靶点之一。在临床前研究模型中,靶向MDSCs在单独给药和联合给药方面均显示出令人鼓舞的结果。在本文中,我们阐述了肝脏的免疫微环境、MDSCs的功能和调节机制以及靶向MDSCs的治疗方法。我们还期望这些策略能为未来肝癌免疫治疗提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/bd90f4f699fa/12672_2023_681_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/74e85d6a0886/12672_2023_681_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/bd90f4f699fa/12672_2023_681_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/74e85d6a0886/12672_2023_681_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/828b/10203092/bd90f4f699fa/12672_2023_681_Fig2_HTML.jpg

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2
"Open Sesame" to the complexity of pattern recognition receptors of myeloid-derived suppressor cells in cancer.揭示髓系来源抑制细胞模式识别受体在癌症中的复杂性。
Front Immunol. 2023 Feb 22;14:1130060. doi: 10.3389/fimmu.2023.1130060. eCollection 2023.
3
Functional states of myeloid cells in cancer.髓系细胞在癌症中的功能状态。
在急性冠脉综合征中,髓系来源的抑制性细胞 CD14HLA-DR 的增加可以作为疾病严重程度和治疗反应的生物标志物。
PeerJ. 2024 Oct 8;12:e18154. doi: 10.7717/peerj.18154. eCollection 2024.
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Dietary vitamin B3 supplementation induces the antitumor immunity against liver cancer via biased GPR109A signaling in myeloid cell.膳食维生素 B3 补充通过髓样细胞中偏向的 GPR109A 信号诱导肝癌的抗肿瘤免疫。
Cell Rep Med. 2024 Sep 17;5(9):101718. doi: 10.1016/j.xcrm.2024.101718.
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IMbrave152/SKYSCRAPER-14: a Phase III study of atezolizumab, bevacizumab and tiragolumab in advanced hepatocellular carcinoma.IMbrave152/SKYSCRAPER-14 研究:阿替利珠单抗、贝伐珠单抗和替西木单抗治疗晚期肝细胞癌的 III 期研究。
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