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肿瘤微环境中巨噬细胞耐受发展的机制。

The Mechanism of the Development of Macrophage Tolerance in Tumor Microenvironment.

机构信息

N. N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow, Russia.

出版信息

Bull Exp Biol Med. 2022 Mar;172(5):653-657. doi: 10.1007/s10517-022-05449-8. Epub 2022 Mar 30.

DOI:10.1007/s10517-022-05449-8
PMID:35352254
Abstract

Bacteria forming the resident microbiome of the tumor are an integral component of its microenvironment. The interaction of the tumor microbiome with the tumor or tumor stromal cells is not well understood. We hypothesized that bacteria in the tumor microenvironment induce macrophage tolerance. Macrophage tolerance is a phenomenon of macrophage inability to respond to a repetitive inflammatory stimulus, which leads to a loss of cytotoxic activity. We studied the development of macrophage tolerance under the influence of bacteria and cytokines of the tumor microenvironment in vitro. It was found that the macrophage tolerance in the tumor stroma can develop in response to bacterial cell wall components and inflammatory factors. The acquired tolerance is inability of macrophages to produce proinflammatory cytokines TNFα, IL-1β, and MCP-1 and activation of the production of immunosuppressive IL-10.

摘要

肿瘤常驻微生物组中的细菌是其微环境的一个组成部分。肿瘤微生物组与肿瘤或肿瘤基质细胞的相互作用还没有被很好地理解。我们假设肿瘤微环境中的细菌会诱导巨噬细胞耐受。巨噬细胞耐受是巨噬细胞无法对重复的炎症刺激作出反应的现象,这导致细胞毒性活性丧失。我们在体外研究了在细菌和肿瘤微环境细胞因子的影响下巨噬细胞耐受的发展。结果发现,肿瘤基质中的巨噬细胞耐受可以对细菌细胞壁成分和炎症因子作出反应而发展。获得性耐受是指巨噬细胞无法产生促炎细胞因子 TNFα、IL-1β 和 MCP-1,并且抑制性细胞因子 IL-10 的产生被激活。

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本文引用的文献

1
The human tumor microbiome is composed of tumor type-specific intracellular bacteria.人类肿瘤微生物组由肿瘤类型特异性的内共生细菌组成。
Science. 2020 May 29;368(6494):973-980. doi: 10.1126/science.aay9189.
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Galactan isolated from Cantharellus cibarius modulates antitumor immune response by converting tumor-associated macrophages toward M1-like phenotype.从鸡油菌中分离出的半乳聚糖通过将肿瘤相关巨噬细胞向 M1 样表型转化来调节抗肿瘤免疫反应。
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Chloroquine modulates antitumor immune response by resetting tumor-associated macrophages toward M1 phenotype.氯喹通过将肿瘤相关巨噬细胞重置为 M1 表型来调节抗肿瘤免疫反应。
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Clin Vaccine Immunol. 2014 Apr;21(4):534-45. doi: 10.1128/CVI.00688-13. Epub 2014 Feb 12.
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Macrophage plasticity and polarization: in vivo veritas.巨噬细胞的可塑性和极化:体内的真实情况。
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Comparative study of tumorigenesis and tumor immunity in invertebrates and nonmammalian vertebrates.无脊椎动物和非哺乳动物脊椎动物的肿瘤发生和肿瘤免疫的比较研究。
Dev Comp Immunol. 2010 Sep;34(9):915-25. doi: 10.1016/j.dci.2010.05.011. Epub 2010 Jun 2.
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miR-146a is critical for endotoxin-induced tolerance: IMPLICATION IN INNATE IMMUNITY.miR-146a 对于内毒素诱导的耐受至关重要:在先天免疫中的意义。
J Biol Chem. 2009 Dec 11;284(50):34590-9. doi: 10.1074/jbc.M109.056317. Epub 2009 Oct 19.
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Endotoxin tolerance: new mechanisms, molecules and clinical significance.内毒素耐受:新机制、分子及临床意义。
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