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活化巨噬细胞杀伤肿瘤细胞的分子机制

Molecular mechanisms in tumor-cell killing by activated macrophages.

作者信息

Adams D O, Nathan C F

机构信息

Departments of Pathology and Microbiology and Immunology, Duke University, Durham, NC 27710, USA.

Department of Cellular Physiology and Immunology, The Rockefeller University, New York, NY 10021, USA.

出版信息

Immunol Today. 1983 Jun;4(6):166-70. doi: 10.1016/0167-5699(83)90005-1.

DOI:10.1016/0167-5699(83)90005-1
PMID:25289537
Abstract

Macrophages kill tumor cells with and without the aid of antibody and evidence suggests that secreted cytotoxic substances are at work in each system. Here Dolph Adams and Carl Nathan discuss the likely involvement in both pathways of several such substances including cytolytic protease and hydrogen peroxide.

摘要

巨噬细胞在有或没有抗体协助的情况下杀死肿瘤细胞,且有证据表明分泌的细胞毒性物质在每个系统中都发挥着作用。在此,多尔夫·亚当斯和卡尔·内森讨论了几种此类物质(包括溶细胞蛋白酶和过氧化氢)可能在这两种途径中所起的作用。

相似文献

1
Molecular mechanisms in tumor-cell killing by activated macrophages.活化巨噬细胞杀伤肿瘤细胞的分子机制
Immunol Today. 1983 Jun;4(6):166-70. doi: 10.1016/0167-5699(83)90005-1.
2
Mechanisms of target recognition and destruction in macrophage-mediated tumor cytotoxicity.巨噬细胞介导的肿瘤细胞毒性中靶点识别与破坏的机制。
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3
Cytolytic mechanisms of activated macrophages. Tumor necrosis factor and L-arginine-dependent mechanisms act synergistically as the major cytolytic mechanisms of activated macrophages.活化巨噬细胞的细胞溶解机制。肿瘤坏死因子和L-精氨酸依赖性机制协同作用,作为活化巨噬细胞的主要细胞溶解机制。
J Immunol. 1990 Feb 15;144(4):1425-31.
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Ex vivo-activated human macrophages kill chronic lymphocytic leukemia cells in the presence of rituximab: mechanism of antibody-dependent cellular cytotoxicity and impact of human serum.体外激活的人巨噬细胞在利妥昔单抗存在的情况下可杀死慢性淋巴细胞白血病细胞:抗体依赖性细胞毒性机制及人血清的影响
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The respiratory burst is not required for killing of intracellular and extracellular parasites by a lymphokine-activated macrophage cell line.淋巴细胞因子激活的巨噬细胞系杀灭细胞内和细胞外寄生虫并不需要呼吸爆发。
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Macrophage-mediated tumor cell killing: regulation of expression of cytolytic activity by prostaglandin E.巨噬细胞介导的肿瘤细胞杀伤作用:前列腺素E对细胞溶解活性表达的调节
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Molecular mechanisms of signal transduction in macrophages.巨噬细胞中信号转导的分子机制。
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Failure of Trypanosoma cruzi to trigger the respiratory burst of activated macrophages. Mechanism for immune evasion and importance of oxygen-independent killing.克氏锥虫无法触发活化巨噬细胞的呼吸爆发。免疫逃避机制及非氧依赖杀伤的重要性。
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Effector mechanisms of the anti-cancer immune responses of macrophages in SR/CR mice.SR/CR小鼠中巨噬细胞抗癌免疫反应的效应机制。
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In vitro generation of human activated lymphocyte killer cells: separate precursors and modes of generation of NK-like cells and "anomalous" killer cells.人活化淋巴细胞杀伤细胞的体外生成:自然杀伤样细胞和“异常”杀伤细胞的不同前体及生成模式。
J Immunol. 1984 Sep;133(3):1656-63.

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Biomedicines. 2022 Aug 15;10(8):1977. doi: 10.3390/biomedicines10081977.
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Production of TNF-alpha, IL-1beta, IL-12 and IFN-gamma in murine peritoneal macrophages on treatment with wheat germ agglutinin in vitro: involvement of tyrosine kinase pathways.体外用麦胚凝集素处理小鼠腹腔巨噬细胞时肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-12和干扰素-γ的产生:酪氨酸激酶途径的参与
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Enhanced killing capacity of human Kupffer cells after activation with human granulocyte/macrophage-colony-stimulating factor and interferon gamma.用人粒细胞/巨噬细胞集落刺激因子和干扰素γ激活后,人库普弗细胞的杀伤能力增强。
Cancer Immunol Immunother. 1994 Sep;39(3):179-84. doi: 10.1007/BF01533384.
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Dynamics of actin filaments in microglia during Fc receptor-mediated phagocytosis.Fc受体介导的吞噬作用过程中小胶质细胞中肌动蛋白丝的动态变化。
Acta Neuropathol. 1994;88(6):527-37. doi: 10.1007/BF00296489.
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Defective interleukin-1 production by monocytes from patients with malignant disease. Interferon increases IL-1 production.恶性疾病患者单核细胞白细胞介素-1产生缺陷。干扰素可增加白细胞介素-1的产生。
Cancer Immunol Immunother. 1984;16(3):182-5. doi: 10.1007/BF00205426.
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Tuftsin induced tumor necrosis activity.
Mol Cell Biochem. 1987 Jun;75(2):169-74. doi: 10.1007/BF00229905.
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Effects of tumor growth on host defenses.肿瘤生长对宿主防御的影响。
Cancer Metastasis Rev. 1986;5(1):15-27. doi: 10.1007/BF00049528.
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The role of phospholipases from inflammatory macrophages in demyelination.炎症巨噬细胞中的磷脂酶在脱髓鞘中的作用。
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Cytotoxic effector cells of the immune system.免疫系统的细胞毒性效应细胞。
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TNF-alpha mediated selection of macrophage-resistant gene-regulatory tumor variants.肿瘤坏死因子-α介导的巨噬细胞抗性基因调控肿瘤变体的选择。
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