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Myeloid-Derived Suppressor Cell Survival and Function Are Regulated by the Transcription Factor Nrf2.髓源性抑制细胞的存活与功能受转录因子Nrf2调控。
J Immunol. 2016 Apr 15;196(8):3470-8. doi: 10.4049/jimmunol.1501785. Epub 2016 Mar 2.
2
High-mobility group box protein 1 promotes the survival of myeloid-derived suppressor cells by inducing autophagy.高迁移率族蛋白1通过诱导自噬促进髓源性抑制细胞的存活。
J Leukoc Biol. 2016 Sep;100(3):463-70. doi: 10.1189/jlb.3HI0715-305R. Epub 2016 Feb 10.
3
Myeloid Cells and Related Chronic Inflammatory Factors as Novel Predictive Markers in Melanoma Treatment with Ipilimumab.髓样细胞及相关慢性炎症因子作为伊匹单抗治疗黑色素瘤的新型预测标志物。
Clin Cancer Res. 2015 Dec 15;21(24):5453-9. doi: 10.1158/1078-0432.CCR-15-0676. Epub 2015 Aug 19.
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Myeloid-Derived Suppressor Cells: Critical Cells Driving Immune Suppression in the Tumor Microenvironment.髓源性抑制细胞:肿瘤微环境中驱动免疫抑制的关键细胞
Adv Cancer Res. 2015;128:95-139. doi: 10.1016/bs.acr.2015.04.002. Epub 2015 May 12.
5
Immunosuppressive and Prometastatic Functions of Myeloid-Derived Suppressive Cells Rely upon Education from Tumor-Associated B Cells.髓源性抑制细胞的免疫抑制和促转移功能依赖于肿瘤相关B细胞的“教育”。
Cancer Res. 2015 Sep 1;75(17):3456-65. doi: 10.1158/0008-5472.CAN-14-3077. Epub 2015 Jul 16.
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Microenvironmental regulation of therapeutic response in cancer.癌症治疗反应的微环境调节
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7
Reduced Myeloid-derived Suppressor Cells in the Blood and Endometrium is Associated with Early Miscarriage.血液和子宫内膜中髓源性抑制细胞减少与早期流产相关。
Am J Reprod Immunol. 2015 Jun;73(6):479-86. doi: 10.1111/aji.12351. Epub 2014 Dec 13.
8
Mast cells boost myeloid-derived suppressor cell activity and contribute to the development of tumor-favoring microenvironment.肥大细胞增强髓源性抑制细胞的活性,并有助于肿瘤有利微环境的发展。
Cancer Immunol Res. 2015 Jan;3(1):85-95. doi: 10.1158/2326-6066.CIR-14-0102. Epub 2014 Oct 28.
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Ubiquitinated proteins in exosomes secreted by myeloid-derived suppressor cells.髓源性抑制细胞分泌的外泌体中的泛素化蛋白。
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10
Cross-talk among myeloid-derived suppressor cells, macrophages, and tumor cells impacts the inflammatory milieu of solid tumors.髓源性抑制细胞、巨噬细胞和肿瘤细胞之间的相互作用影响实体瘤的炎症环境。
J Leukoc Biol. 2014 Dec;96(6):1109-18. doi: 10.1189/jlb.3A0414-210R. Epub 2014 Aug 28.

肿瘤微环境中的耐受性与免疫抑制

Tolerance and immune suppression in the tumor microenvironment.

作者信息

Ostrand-Rosenberg Suzanne

机构信息

Dept. of Biological Sciences, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, United States.

出版信息

Cell Immunol. 2016 Jan;299:23-9. doi: 10.1016/j.cellimm.2015.09.011. Epub 2015 Sep 30.

DOI:10.1016/j.cellimm.2015.09.011
PMID:26435343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4698223/
Abstract

The concept of immunological tolerance has guided and permeated much of modern immunology. Ray Owen's ground-breaking observations in twin cattle provided the first mechanistic explanation for tolerance to self-molecules and established tolerance as a beneficial process that protects the host against autoreactivity. However, his studies also opened the door to understanding that tolerance may be detrimental, such as occurs when cancer cells induce tolerance/immune suppression resulting in inhibition of anti-tumor immunity. This article briefly traces the early history of the field of tumor immunology with respect to tolerance, and then focuses on a relatively recently identified population of cells called myeloid-derived suppressor cells (MDSCs). MDSC are instrumental in causing tolerance/immune suppression in individuals with cancer. They are present in most individuals with cancer and because of their potent immune suppressive activity are a major deterrent to natural anti-tumor immunity and a significant obstacle to immunotherapy.

摘要

免疫耐受的概念贯穿并指导了现代免疫学的许多方面。雷·欧文对孪生牛的开创性观察为自身分子耐受提供了首个机理解释,并确立了耐受是一种保护宿主免受自身反应性侵害的有益过程。然而,他的研究也开启了人们对耐受可能有害的认识,比如癌细胞诱导耐受/免疫抑制从而抑制抗肿瘤免疫时的情况。本文简要追溯了肿瘤免疫学领域中关于耐受的早期历史,然后重点关注一类相对较新发现的细胞群,即髓源性抑制细胞(MDSC)。MDSC在导致癌症患者出现耐受/免疫抑制方面发挥着作用。它们存在于大多数癌症患者体内,由于其强大的免疫抑制活性,是天然抗肿瘤免疫的主要阻碍以及免疫治疗的重大障碍。