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找到你的利基:静止肿瘤库中的免疫逃逸。

Finding your niche: immune evasion in quiescent tumor reservoirs.

机构信息

Division of Biological Sciences, University of California, San Diego, CA 92093, USA.

Division of Biological Sciences, University of California, San Diego, CA 92093, USA.

出版信息

Trends Immunol. 2022 Jul;43(7):500-502. doi: 10.1016/j.it.2022.05.003. Epub 2022 Jun 5.

DOI:10.1016/j.it.2022.05.003
PMID:35672237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9674368/
Abstract

Emerging immunotherapies offer a new hope for cancer patients but are not always effective even when a tumor is recognized by the immune system. Baldominos and colleagues address this challenge by characterizing a resilient niche of metabolically unique quiescent cancer cells (QCCs) that resist T cell-mediated control.

摘要

新兴的免疫疗法为癌症患者带来了新的希望,但即使肿瘤被免疫系统识别,这些疗法也并不总是有效。Baldominos 及其同事通过描述代谢上独特的静止癌细胞(QCC)的弹性小生境来应对这一挑战,这些 QCC 能够抵抗 T 细胞介导的控制。

相似文献

1
Finding your niche: immune evasion in quiescent tumor reservoirs.找到你的利基:静止肿瘤库中的免疫逃逸。
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Mechanisms of HIF1A-mediated immune evasion in gastric cancer and the impact on therapy resistance.HIF1A 介导的胃癌免疫逃逸机制及其对治疗抵抗的影响。
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Quiescent cancer cells resist T cell attack by forming an immunosuppressive niche.静止期癌细胞通过形成免疫抑制微环境来抵抗 T 细胞攻击。
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本文引用的文献

1
Quiescent cancer cells resist T cell attack by forming an immunosuppressive niche.静止期癌细胞通过形成免疫抑制微环境来抵抗 T 细胞攻击。
Cell. 2022 May 12;185(10):1694-1708.e19. doi: 10.1016/j.cell.2022.03.033. Epub 2022 Apr 20.
2
Transforming growth factor-β-regulated mTOR activity preserves cellular metabolism to maintain long-term T cell responses in chronic infection.转化生长因子-β调节的 mTOR 活性可维持细胞代谢,以保持慢性感染中 T 细胞的长期应答。
Immunity. 2021 Aug 10;54(8):1698-1714.e5. doi: 10.1016/j.immuni.2021.06.007. Epub 2021 Jul 6.
3
Towards a Framework for Better Understanding of Quiescent Cancer Cells.迈向更好理解静止癌细胞的框架。
Cells. 2021 Mar 5;10(3):562. doi: 10.3390/cells10030562.
4
Infection and cancer suppress pDC derived IFN-I.感染和癌症抑制 pDC 产生的 IFN-I。
Curr Opin Immunol. 2020 Oct;66:114-122. doi: 10.1016/j.coi.2020.08.001. Epub 2020 Sep 15.
5
Single-Cell RNA Sequencing Reveals Stromal Evolution into LRRC15 Myofibroblasts as a Determinant of Patient Response to Cancer Immunotherapy.单细胞 RNA 测序揭示了间质向 LRRC15 肌成纤维细胞的演化是决定癌症免疫治疗患者反应的决定因素。
Cancer Discov. 2020 Feb;10(2):232-253. doi: 10.1158/2159-8290.CD-19-0644. Epub 2019 Nov 7.
6
Dendritic Cell Metabolism and Function in Tumors.树突状细胞代谢与肿瘤功能
Trends Immunol. 2019 Aug;40(8):699-718. doi: 10.1016/j.it.2019.06.004. Epub 2019 Jul 10.
7
Genomic correlates of response to immune checkpoint blockade.免疫检查点阻断治疗反应的基因组相关性。
Nat Med. 2019 Mar;25(3):389-402. doi: 10.1038/s41591-019-0382-x. Epub 2019 Mar 6.
8
CD8 T Cell Exhaustion During Chronic Viral Infection and Cancer.慢性病毒感染和癌症中的 CD8 T 细胞耗竭。
Annu Rev Immunol. 2019 Apr 26;37:457-495. doi: 10.1146/annurev-immunol-041015-055318. Epub 2019 Jan 24.
9
Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments.Foxp3重编程T细胞代谢以在低糖、高乳酸环境中发挥功能。
Cell Metab. 2017 Jun 6;25(6):1282-1293.e7. doi: 10.1016/j.cmet.2016.12.018. Epub 2017 Apr 13.
10
GFP-specific CD8 T cells enable targeted cell depletion and visualization of T-cell interactions.绿色荧光蛋白特异性CD8 T细胞可实现靶向细胞清除并可视化T细胞相互作用。
Nat Biotechnol. 2015 Dec;33(12):1287-1292. doi: 10.1038/nbt.3386. Epub 2015 Nov 2.