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本文引用的文献

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Identification of monocyte-like precursors of granulocytes in cancer as a mechanism for accumulation of PMN-MDSCs.鉴定癌症中粒细胞样单核细胞前体细胞作为 PMN-MDSC 积累的机制。
J Exp Med. 2019 Sep 2;216(9):2150-2169. doi: 10.1084/jem.20181952. Epub 2019 Jun 25.
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iDEP: an integrated web application for differential expression and pathway analysis of RNA-Seq data.iDEP:一个用于 RNA-Seq 数据差异表达和通路分析的集成网络应用程序。
BMC Bioinformatics. 2018 Dec 19;19(1):534. doi: 10.1186/s12859-018-2486-6.
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Characterization of Human Monocyte Subsets by Whole Blood Flow Cytometry Analysis.通过全血流式细胞术分析对人单核细胞亚群进行表征
J Vis Exp. 2018 Oct 17(140):57941. doi: 10.3791/57941.
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Developmental and Functional Heterogeneity of Monocytes.单核细胞的发育和功能异质性。
Immunity. 2018 Oct 16;49(4):595-613. doi: 10.1016/j.immuni.2018.10.005.
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How to measure the immunosuppressive activity of MDSC: assays, problems and potential solutions.如何测量 MDSC 的免疫抑制活性:检测方法、问题及潜在解决方案。
Cancer Immunol Immunother. 2019 Apr;68(4):631-644. doi: 10.1007/s00262-018-2170-8. Epub 2018 May 21.
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The pro-inflammatory phenotype of the human non-classical monocyte subset is attributed to senescence.人类非经典单核细胞亚群的促炎表型归因于衰老。
Cell Death Dis. 2018 Feb 15;9(3):266. doi: 10.1038/s41419-018-0327-1.
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Granulocyte-Monocyte Progenitors and Monocyte-Dendritic Cell Progenitors Independently Produce Functionally Distinct Monocytes.粒细胞-单核细胞祖细胞和单核细胞-树突状细胞祖细胞独立产生功能不同的单核细胞。
Immunity. 2017 Nov 21;47(5):890-902.e4. doi: 10.1016/j.immuni.2017.10.021.
8
The fate and lifespan of human monocyte subsets in steady state and systemic inflammation.稳态和全身炎症状态下人类单核细胞亚群的命运与寿命。
J Exp Med. 2017 Jul 3;214(7):1913-1923. doi: 10.1084/jem.20170355. Epub 2017 Jun 12.
9
Splicing modulators act at the branch point adenosine binding pocket defined by the PHF5A-SF3b complex.剪接调节剂作用于由 PHF5A-SF3b 复合物定义的分支点腺苷结合口袋。
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Genomic Characterization of Murine Monocytes Reveals C/EBPβ Transcription Factor Dependence of Ly6C Cells.鼠源单核细胞的基因组特征揭示了 C/EBPβ 转录因子对 Ly6C 细胞的依赖性。
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CD66b 单核细胞代表癌症中促炎的髓系亚群。

CD66b monocytes represent a proinflammatory myeloid subpopulation in cancer.

机构信息

Department of Basic Oncology, Hacettepe University Cancer Institute, 06230, Ankara, Turkey.

Department of Immunology, Faculty of Medicine, Bursa Uludag University, Bursa, Turkey.

出版信息

Cancer Immunol Immunother. 2021 Jan;70(1):75-87. doi: 10.1007/s00262-020-02656-y. Epub 2020 Jul 6.

DOI:10.1007/s00262-020-02656-y
PMID:32632664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10992132/
Abstract

Myeloid-derived suppressor cells (MDSC) populate the peripheral blood and contribute to immune regulation in cancer. However, there is limited knowledge on the myeloid cell types with proinflammatory capacities that may serve as opponents of MDSC. In the circulation of cancer patients, a monocyte subpopulation was identified with a specific immunophenotype and transcriptomic signature. They were predominantly CD14CD33CD16HLA-DR cells that typically expressed CD66b. In accordance with the transcriptomics data, NALP3, LOX-1 and PAI-1 levels were also significantly upregulated. The CD66b monocytes displayed high phagocytic activity, matrix adhesion and migration, and provided costimulation for T cell proliferation and IFN-γ secretion; thus, they did not suppress T cell responses. Irrespective of clinical stage, they were identified in various cancers. In conclusion, the CD66b monocytes represent a novel myeloid subpopulation which is devoid of immune regulatory influences of cancer and displays enhanced proinflammatory capacities.

摘要

髓系来源的抑制细胞(MDSC)存在于外周血中,并参与癌症的免疫调节。然而,对于具有促炎能力的髓系细胞类型,我们知之甚少,这些细胞可能是 MDSC 的拮抗物。在癌症患者的循环中,鉴定出一种具有特定免疫表型和转录组特征的单核细胞亚群。它们主要是 CD14CD33CD16HLA-DR 细胞,通常表达 CD66b。根据转录组学数据,NALP3、LOX-1 和 PAI-1 的水平也显著上调。CD66b 单核细胞表现出高吞噬活性、基质黏附和迁移,并为 T 细胞增殖和 IFN-γ 分泌提供共刺激作用;因此,它们不会抑制 T 细胞反应。无论临床分期如何,它们都存在于各种癌症中。总之,CD66b 单核细胞代表了一种新型的髓系亚群,它没有癌症的免疫调节影响,并显示出增强的促炎能力。