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本文引用的文献

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Recognition of cytosolic DNA by cGAS and other STING-dependent sensors.环鸟苷酸-腺苷酸合成酶(cGAS)和其他 STING 依赖性传感器对细胞质 DNA 的识别。
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Commensal bacteria control cancer response to therapy by modulating the tumor microenvironment.共生菌通过调节肿瘤微环境来控制癌症对治疗的反应。
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Interferon-dependent IL-10 production by Tregs limits tumor Th17 inflammation.调节性 T 细胞依赖干扰素产生的白细胞介素 10 限制肿瘤 Th17 炎症。
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Inflammation-induced cancer: crosstalk between tumours, immune cells and microorganisms.炎症相关癌症:肿瘤、免疫细胞和微生物之间的串扰。
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Spatiotemporal dynamics of intratumoral immune cells reveal the immune landscape in human cancer.肿瘤内免疫细胞的时空动态揭示了人类癌症中的免疫景观。
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Nature. 2013 Oct 31;502(7473):637-43. doi: 10.1038/nature12612. Epub 2013 Oct 9.
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Hypoxia-inducible factors enhance the effector responses of CD8(+) T cells to persistent antigen.缺氧诱导因子增强 CD8(+) T 细胞对持续性抗原的效应反应。
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Mucus enhances gut homeostasis and oral tolerance by delivering immunoregulatory signals.黏液通过传递免疫调节信号来增强肠道稳态和口腔耐受。
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宿主对感染和癌症的免疫反应:出人意料的共同之处。

Host immune response to infection and cancer: unexpected commonalities.

机构信息

Cancer and Inflammation Program, National Cancer Institute, Frederick, MD 21702, USA.

Cancer and Inflammation Program, National Cancer Institute, Frederick, MD 21702, USA; Leidos Biomedical Research, Inc., Frederick, MD 21701, USA.

出版信息

Cell Host Microbe. 2014 Mar 12;15(3):295-305. doi: 10.1016/j.chom.2014.02.003.

DOI:10.1016/j.chom.2014.02.003
PMID:24629336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3996827/
Abstract

Both microbes and tumors activate innate resistance, tissue repair, and adaptive immunity. Unlike acute infection, tumor growth is initially unapparent; however, inflammation and immunity affect all phases of tumor growth from initiation to progression and dissemination. Here, we discuss the shared features involved in the immune response to infection and cancer including modulation by commensal microbiota, reactive hematopoiesis, chronic immune responses and regulatory mechanisms to prevent collateral tissue damage. This comparative analysis of immunity to infection and cancer furthers our understanding of the basic mechanisms underlying innate resistance and adaptive immunity and their translational application to the design of new therapeutic approaches.

摘要

微生物和肿瘤均可激活固有免疫、组织修复和适应性免疫。与急性感染不同,肿瘤生长起初并不明显;然而,炎症和免疫会影响肿瘤生长的各个阶段,从起始到进展和扩散。在这里,我们讨论了感染和癌症免疫反应所涉及的共同特征,包括共生微生物群的调节、反应性造血、慢性免疫反应和防止继发组织损伤的调节机制。这种对感染和癌症免疫的比较分析增进了我们对固有抵抗和适应性免疫基本机制的理解,并将其转化应用于新治疗方法的设计。